Various rising carbon seize applied sciences depend upon having the ability to reliably and persistently develop carbon dioxide hydrate, notably in packed media. However, there are restricted kinetic knowledge for carbon dioxide hydrates at this size scale. In this work, carbon dioxide hydrate propagation charges and conversion have been evaluated in a excessive stress silicon microfluidic gadget. The carbon dioxide part boundary was first measured in the microfluidic gadget, which confirmed little deviation from bulk predictions. Additionally, measuring the part boundary takes on the order of hours in comparison with weeks or longer for bigger scale experimental setups.
Next, propagation charges of carbon dioxide hydrate have been measured in the channels at low subcoolings (<2 Okay from part boundary) and reasonable pressures (200-500 psi). Growth was dominated by mass switch limitations till a crucial stress was reached, and response kinetics restricted development upon additional will increase in stress. Additionally, hydrate conversion was estimated from Raman spectroscopy in the microfluidics channels. A most worth of 47% conversion was reached inside 1 h of a fixed stream experiment, almost 4% of the time required for comparable outcomes in a giant scale system. The fast response instances and excessive throughput allowed by excessive stress microfluidics present a new method for carbon dioxide gasoline hydrate to be characterised.
The proposed technique consists of picture restoration, picture segmentation, crystal measurement measurement, and measurement prediction. To cope with the consequences of noise air pollution, uneven illumination and motion blurring, the picture processing technique is performed for segmenting crystal photographs captured from the stirring reactor. Thus, the crystal measurement distribution for crystal inhabitants is obtained through the use of a chance density operate. In addition, a short-term prediction technique is given for crystal sizes. An experimental research on the cooling crystallization strategy of β-form LGA is proven to reveal the effectiveness of the proposed technique.
On the Gibbs-Thomson equation for the crystallization of confined fluids
The Gibbs-Thomson (GT) equation describes the shift of the crystallization temperature for a confined fluid with respect to the majority as a operate of pore measurement. While this century previous relation is efficiently used to research experiments, its derivations discovered in the literature typically depend on nucleation principle arguments (i.e., kinetics as an alternative of thermodynamics) or fail to state their assumptions, subsequently resulting in comparable however completely different expressions. Here, we revisit the derivation of the GT equation to make clear the system definition, corresponding thermodynamic ensemble, and assumptions made alongside the way in which.
We additionally focus on the position of the thermodynamic situations in the exterior reservoir on the ultimate end result. We then flip to numerical simulations of a mannequin system to compute independently the varied phrases getting into in the GT equation and evaluate the predictions of the latter with the melting temperatures decided beneath confinement via hyper-parallel tempering grand canonical Monte Carlo simulations. We spotlight some difficulties associated to the sampling of crystallization beneath confinement in simulations.
This strategy might, for instance, be used to analyze the nanoscale capillary freezing of ionic liquids lately noticed experimentally between the tip of an atomic drive microscope and a substrate. In this paper, a crystal picture evaluation technique is offered to measure and predict crystal sizes, primarily based on cooling crystallization of β-form L-glutamic acid (LGA) through the use of an in-situ non-invasive imaging system. Overall, regardless of its limitations, the GT equation might present an fascinating different path to predict the melting temperature in giant pores utilizing molecular simulations to judge the related portions getting into in this equation.

Simulation Study on Prediction of Urea Crystallization of a Diesel Engine Integrated after-Treatment Device
An built-in after-treatment gadget mannequin was established for our goal engine primarily based on the fluid simulation software program (Converge), and simulation was carried out to find out the NH3, temperature, and velocity uniformity on the front-end cross part of its SCR catalyst, urea deposition fee, liquid movie mass of the mixer, and its positions beneath a low-load situation. Moreover, the construction of the mixer and injection stress have been optimized to enhance the uniformity and cut back the liquid movie mass.
Our simulation outcomes present the next information: the liquid movie is definitely collected beneath a low-load situation and the construction of the mixer and the injection stress considerably have an effect on the urea deposition fee and uniformities and accumulation plenty of the liquid movie. As a end result, our remaining optimization outcomes point out that the mass of the NH3 and the NH3 uniformity on the front-end cross part of the SCR catalyst enhance by 2.83 instances and 5.65%. The urea deposition fee and the cumulative mass of the liquid movie fall by 4.82 and 10.4%, respectively. This research has sure theoretical guiding significance for the optimum design of one of these after-treatment units.
Membrane Protein Extraction Kit |
K3014005 |
Biochain |
1 kit |
EUR 382 |
Description: Can be used for various proteomics studies in both normal and pathological cases. It is an excellent control and suitable for educational purposes. This product is prepared from whole tissue homogenates and has undergone SDS-PAGE quality control analysis. The protein is stored in a buffer with protease inhibitor cocktail fo prevent degradation. |
Membrane Cofactor Protein (CD46) Protein |
20-abx261046 |
Abbexa |
-
EUR 3418.00
-
EUR 328.00
-
EUR 230.00
|
|
|
Golgi Membrane Protein 1 Protein |
20-abx262719 |
Abbexa |
-
EUR 328.00
-
EUR 6397.00
-
EUR 230.00
|
|
|
Dialysis Membrane |
2392344 |
Atto |
8unit |
EUR 276 |
Membrane Remover |
MVSMR100 |
Neuromics |
Complete |
EUR 2653 |
Spoligotyping Membrane |
IM9702 |
Mapmygenome |
|
EUR 1280 |
Description: A very simple, inexpensive and effective tool for Tuberculosis/ Mycobacterium research. Spoligotyping is a PCR-based Method to Simultaneously Detect and Type Mycobacterium Tuberculosis Complex Bacteria. Spoligotyping, which uses RLB (Reversed Line Blotting) offers an alternative for typical Southern blotting when rapid results are required. The method is particularly useful to simultaneously detect and type M. tuberculosis complex bacteria in clinical samples (suspected nosocomial infections, outbreaks in prisons, etc.). The level of differentiation by spoligotyping is less compared to IS6110 fingerprinting for strains having five or more IS6110 copies, but higher for strains with less than five copies. Thus, Spoligotyping is a preferred method to type M. bovis strains, which usually contain only one or two IS6110 copies. Note, that Mycobacterium bovis can be recognized by the absence of reactivity with spacers 39-43. |
Membrane Protein FAM174A (FAM174A) Antibody |
20-abx301608 |
Abbexa |
-
EUR 411.00
-
EUR 1845.00
-
EUR 599.00
-
EUR 182.00
-
EUR 300.00
|
- 100 ug
- 1 mg
- 200 ug
- 20 ug
- 50 ug
|
|
Membrane Protein MLC1 (MLC1) Antibody |
20-abx302145 |
Abbexa |
-
EUR 411.00
-
EUR 1845.00
-
EUR 599.00
-
EUR 182.00
-
EUR 300.00
|
- 100 ug
- 1 mg
- 200 ug
- 20 ug
- 50 ug
|
|
Membrane Cofactor Protein (CD46) Antibody |
20-abx302453 |
Abbexa |
-
EUR 411.00
-
EUR 1845.00
-
EUR 599.00
-
EUR 182.00
-
EUR 300.00
|
- 100 ug
- 1 mg
- 200 ug
- 20 ug
- 50 ug
|
|
Mammalian Membrane Protein Extraction Kit |
AR0155 |
BosterBio |
1 kit |
EUR 152 |
Outer membrane protein A Antibody |
20-abx110631 |
Abbexa |
-
EUR 411.00
-
EUR 1845.00
-
EUR 599.00
-
EUR 182.00
-
EUR 300.00
|
- 100 ug
- 1 mg
- 200 ug
- 20 ug
- 50 ug
|
|
Membrane Protein MLC1 (MLC1) Antibody |
20-abx113650 |
Abbexa |
|
|
|
Membrane Cofactor Protein (MCP) Antibody |
20-abx102461 |
Abbexa |
-
EUR 411.00
-
EUR 133.00
-
EUR 1149.00
-
EUR 565.00
-
EUR 314.00
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Membrane Cofactor Protein (MCP) Antibody |
20-abx102462 |
Abbexa |
-
EUR 425.00
-
EUR 133.00
-
EUR 1177.00
-
EUR 578.00
-
EUR 328.00
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Membrane Cofactor Protein (MCP) Antibody |
20-abx102463 |
Abbexa |
-
EUR 439.00
-
EUR 133.00
-
EUR 1247.00
-
EUR 592.00
-
EUR 328.00
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Glomerular Basement Membrane (GBM) Protein |
abx061497-200ug |
Abbexa |
200 ug |
EUR 1539 |
|
Campylobacter jejuni outer membrane Protein |
abx061523-100ug |
Abbexa |
100 ug |
EUR 1010 |
|
Entamoeba dispar outer membrane Protein |
abx061530-100ug |
Abbexa |
100 ug |
EUR 1010 |
|
Mammalian Membrane Protein Extraction Kit |
20-abx098855 |
Abbexa |
|
|
|
Membrane Cofactor Protein (CD46) Antibody |
abx034950-400ul |
Abbexa |
400 ul |
EUR 523 |
|
Membrane Cofactor Protein (CD46) Antibody |
abx034950-80l |
Abbexa |
80 µl |
EUR 286 |
|
Membrane Cofactor Protein (CD46) Antibody |
20-abx001390 |
Abbexa |
-
EUR 411.00
-
EUR 592.00
-
EUR 182.00
-
EUR 314.00
|
- 100 ul
- 200 ul
- 20 ul
- 50 ul
|
|
Membrane Protein MLC1 (MLC1) Antibody |
abx030675-400ul |
Abbexa |
400 ul |
EUR 523 |
|
Membrane Protein MLC1 (MLC1) Antibody |
abx030675-80l |
Abbexa |
80 µl |
EUR 286 |
|
Membrane Cofactor Protein (CD46) Antibody |
abx032307-400ul |
Abbexa |
400 ul |
EUR 523 |
|
Membrane Cofactor Protein (CD46) Antibody |
abx032307-80l |
Abbexa |
80 µl |
EUR 286 |
|
EMP-1 (Epithelial Membrane Protein) |
5-01091 |
CHI Scientific |
4 x 1mg |
Ask for price |
Membrane Protein MLC1 (MLC1) Antibody |
abx432971-200ul |
Abbexa |
200 ul |
EUR 384 |
|
Helicobacter Pylori Outer Membrane Protein |
20-abx260304 |
Abbexa |
-
EUR 885.00
-
EUR 342.00
-
EUR 1609.00
|
|
|
Prostate Specific Membrane Antigen Protein |
20-abx263559 |
Abbexa |
-
EUR 829.00
-
EUR 411.00
-
EUR 537.00
|
|
|
Membrane Cofactor Protein (CD46) Antibody |
20-abx339216 |
Abbexa |
|
|
|
Membrane Cofactor Protein (CD46) Antibody |
20-abx339217 |
Abbexa |
|
|
|
Membrane Cofactor Protein (MCP) Antibody |
20-abx173533 |
Abbexa |
|
|
|
Prolytic Membrane Protein Extraction Kit |
P6300-020 |
GenDepot |
20 prep |
EUR 266 |
Prolytic Membrane Protein Extraction Kit |
P6300-050 |
GenDepot |
50 prep |
EUR 469 |
Mouse Membrane cofactor protein (Cd46) |
1-CSB-EP004939MO |
Cusabio |
-
EUR 505.00
-
EUR 265.00
-
EUR 1827.00
-
EUR 766.00
-
EUR 1218.00
-
EUR 335.00
|
- 100ug
- 10ug
- 1MG
- 200ug
- 500ug
- 50ug
|
|
Description: Recombinant Mouse Membrane cofactor protein(Cd46) ,partial expressed in E.coli |
Recombinant Membrane Cofactor Protein (MCP) |
4-RPB275Hu01 |
Cloud-Clone |
-
EUR 485.28
-
EUR 233.00
-
EUR 1544.80
-
EUR 581.60
-
EUR 1063.20
-
EUR 388.00
-
EUR 3712.00
|
- 100 ug
- 10ug
- 1 mg
- 200 ug
- 500 ug
- 50ug
- 5 mg
|
|
Description: Recombinant Human Membrane Cofactor Protein expressed in: E.coli |
Recombinant Membrane Cofactor Protein (MCP) |
4-RPB275Mu01 |
Cloud-Clone |
-
EUR 494.24
-
EUR 235.00
-
EUR 1578.40
-
EUR 592.80
-
EUR 1085.60
-
EUR 394.00
-
EUR 3796.00
|
- 100 ug
- 10ug
- 1 mg
- 200 ug
- 500 ug
- 50ug
- 5 mg
|
|
Description: Recombinant Mouse Membrane Cofactor Protein expressed in: E.coli |
Recombinant Membrane Cofactor Protein (MCP) |
4-RPB275Ra01 |
Cloud-Clone |
-
EUR 515.74
-
EUR 241.00
-
EUR 1659.04
-
EUR 619.68
-
EUR 1139.36
-
EUR 408.00
-
EUR 3997.60
|
- 100 ug
- 10ug
- 1 mg
- 200 ug
- 500 ug
- 50ug
- 5 mg
|
|
Description: Recombinant Rat Membrane Cofactor Protein expressed in: E.coli |
Membrane Protein from Lupus: Kidney |
P3236142Lup |
Biochain |
0.1 mg |
EUR 408 |
Description: Can be used for various proteomics studies in both normal and pathological cases. It is an excellent control and suitable for educational purposes. This product is prepared from whole tissue homogenates and has undergone SDS-PAGE quality control analysis. The protein is stored in a buffer with protease inhibitor cocktail fo prevent degradation. |
SARS Coronavirus Membrane Recombinant protein |
39-107 |
ProSci |
0.05 mg |
EUR 464 |
Description: SARS Membrane protein is a membranal protein which plays a crucial role in the virus’ life cycle. This protein has 3 outer cell structural antigens, the envelope (E), membrane (M)and spike (S) antigens. SARS Membrane protein is essential to the process of assembly, budding, creation of the envelope and pathogenesis. |
Human Golgi membrane protein GP73 Protein |
abx060158-100ug |
Abbexa |
100 ug |
EUR 1135 |
|
Human Membrane Cofactor Protein (MCP) Protein |
20-abx067989 |
Abbexa |
-
EUR 676.00
-
EUR 286.00
-
EUR 2082.00
-
EUR 801.00
-
EUR 481.00
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Rat Membrane Cofactor Protein (MCP) Protein |
20-abx067990 |
Abbexa |
-
EUR 718.00
-
EUR 286.00
-
EUR 2235.00
-
EUR 857.00
-
EUR 509.00
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Mouse Membrane Cofactor Protein (MCP) Protein |
20-abx067991 |
Abbexa |
-
EUR 690.00
-
EUR 286.00
-
EUR 2124.00
-
EUR 815.00
-
EUR 495.00
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Vesicle-Associated Membrane Protein 7 Protein |
20-abx260935 |
Abbexa |
-
EUR 3418.00
-
EUR 328.00
-
EUR 230.00
|
|
|
CXADR-Like Membrane Protein (CLMP) Protein |
20-abx261302 |
Abbexa |
-
EUR 3418.00
-
EUR 328.00
-
EUR 230.00
|
|
|
Lysosomal-Associated Membrane Protein 2 Protein |
20-abx262567 |
Abbexa |
-
EUR 328.00
-
EUR 6397.00
-
EUR 230.00
|
|
|
Vesicle-Associated Membrane Protein 4 Protein |
20-abx262862 |
Abbexa |
-
EUR 328.00
-
EUR 6397.00
-
EUR 230.00
|
|
|
Bacterial Outer Membrane Protein-A Protein |
20-abx263222 |
Abbexa |
-
EUR 481.00
-
EUR 1790.00
-
EUR 578.00
|
|
|
Probable outer membrane protein pmp10 Protein |
20-abx600004 |
Abbexa |
-
EUR 2207.00
-
EUR 4351.00
-
EUR 2834.00
-
EUR 1567.00
|
|
|
Probable outer membrane protein pmp10 Protein |
20-abx600017 |
Abbexa |
-
EUR 2875.00
-
EUR 1678.00
-
EUR 1873.00
-
EUR 1274.00
|
|
|
Probable outer membrane protein pmp10 Protein |
20-abx600018 |
Abbexa |
-
EUR 2277.00
-
EUR 1428.00
-
EUR 1553.00
-
EUR 1094.00
|
|
|
Probable outer membrane protein pmp10 Protein |
20-abx600019 |
Abbexa |
|
|
|
Golgi Membrane Protein 1 Recombinant Protein |
91-689 |
ProSci |
0.05 mg |
EUR 542.75 |
Description: Golgi Membrane Protein 1 (GOLM1) belongs to the GOLM1/CASC4 family, GOLM1 is a single-pass type II membrane protein and can be found in many tissues . GOLM1 is overexpressed in prostate cancer and lung adenocarcinoma tissue. GOLM1 can be up-regulated in response to viral infection. GOLM1 is induced by the E1A adenoviral protein. GOLM1 plays a key role in the sorting and modification of proteins exported from the endoplasmic reticulum. |
Campylobacter coli outer membrane protein (OMP) Protein |
abx061519-100ug |
Abbexa |
100 ug |
EUR 1010 |
|
Salmonella Typhi Outer Membrane Protein (omp) Protein |
abx061570-1mg |
Abbexa |
1 mg |
EUR 1790 |
|
Human Membrane Protein, Palmitoylated 2 (MPP2) Protein |
20-abx167830 |
Abbexa |
-
EUR 718.00
-
EUR 286.00
-
EUR 2207.00
-
EUR 843.00
-
EUR 509.00
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Mouse Membrane Protein, Palmitoylated 6 (MPP6) Protein |
20-abx167831 |
Abbexa |
-
EUR 732.00
-
EUR 286.00
-
EUR 2263.00
-
EUR 871.00
-
EUR 523.00
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Salmonella Enteritidis Outer Membrane Protein-A Protein |
20-abx260301 |
Abbexa |
-
EUR 885.00
-
EUR 342.00
-
EUR 1609.00
|
|
|
Borrelia Burgdorferi Basic Membrane Protein A Protein |
20-abx261860 |
Abbexa |
-
EUR 4490.00
-
EUR 328.00
-
EUR 230.00
|
|
|
Borrelia Afzelii Basic Membrane Protein A Protein |
20-abx261866 |
Abbexa |
-
EUR 4490.00
-
EUR 328.00
-
EUR 230.00
|
|
|
Zymogen Granule Membrane Protein 16 (ZG16) Protein |
20-abx263238 |
Abbexa |
-
EUR 1609.00
-
EUR 328.00
-
EUR 230.00
|
|
|
Human Membrane Protein, Palmitoylated 5 (MPP5) Protein |
20-abx165876 |
Abbexa |
-
EUR 690.00
-
EUR 286.00
-
EUR 2124.00
-
EUR 815.00
-
EUR 495.00
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Human Membrane Protein, Palmitoylated 6 (MPP6) Protein |
20-abx165878 |
Abbexa |
-
EUR 718.00
-
EUR 286.00
-
EUR 2221.00
-
EUR 857.00
-
EUR 509.00
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Mouse Membrane Protein, Palmitoylated 2 (MPP2) Protein |
20-abx165880 |
Abbexa |
-
EUR 732.00
-
EUR 286.00
-
EUR 2305.00
-
EUR 885.00
-
EUR 523.00
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Human Epithelial Membrane Protein 3 (EMP3) Protein |
20-abx653303 |
Abbexa |
-
EUR 578.00
-
EUR 258.00
-
EUR 1720.00
-
EUR 690.00
-
EUR 425.00
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Rat Membrane Protein, Palmitoylated 2 (MPP2) Protein |
20-abx654340 |
Abbexa |
-
EUR 578.00
-
EUR 258.00
-
EUR 1720.00
-
EUR 690.00
-
EUR 425.00
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Human Membrane Protein, Palmitoylated 3 (MPP3) Protein |
20-abx650281 |
Abbexa |
-
EUR 592.00
-
EUR 258.00
-
EUR 1748.00
-
EUR 690.00
-
EUR 425.00
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Rat Membrane Protein, Palmitoylated 3 (MPP3) Protein |
20-abx650282 |
Abbexa |
-
EUR 634.00
-
EUR 272.00
-
EUR 1929.00
-
EUR 759.00
-
EUR 467.00
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Mouse Glycosylated Lysosomal Membrane Protein (GLMP) Protein |
20-abx650833 |
Abbexa |
-
EUR 690.00
-
EUR 286.00
-
EUR 2124.00
-
EUR 815.00
-
EUR 495.00
|
- 100 ug
- 10 ug
- 1 mg
- 200 ug
- 50 ug
|
|
Porcine Vesicle- associated membrane protein- associated protein |
ELI-44663p |
Lifescience Market |
96 Tests |
EUR 928 |
Nylon Membrane (30cmx3m) |
D0157-3 |
Bio Basic |
1(30cmx3m), 1 UNIT |
EUR 869.25 |
|
Nitrocellulose Membrane 0.22um |
NT020S1 |
Bio Basic |
5(20x20cm), 5UNIT |
EUR 126.56 |
|
Dialysis membrane, 34mm |
TX0111 |
Bio Basic |
2m, 2m |
EUR 65.66 |
|
Dialysis membrane, 44mm |
TX0112 |
Bio Basic |
2m, 2m |
EUR 69.14 |
|
Dialysis membrane, 77mm |
TX0113 |
Bio Basic |
2m, 2m |
EUR 77.84 |
|
Nitrocellulose Membrane Roll |
B500 |
ABM |
3m x 30cm Roll |
EUR 272 |
Nitrocellulose Membrane Precut |
B501 |
ABM |
Pack of 30, 6cm x 8.5cm |
EUR 124 |
TMB Membrane Substrate |
42-TB07 |
Fitzgerald |
100 ml |
EUR 132 |
Description: High sensitivity HRP membrane substrate (containing TMB) |
Zika Membrane Peptide |
8667P |
ProSci |
0.05 mg |
EUR 164.75 |
Description: Zika Membrane Peptide |
Brain Membrane Lysate |
21-138 |
ProSci |
0.1 mg |
EUR 569 |
Description: Monkey (Cynomolgus) brain tissue membrane protein lysate was prepared by homogenization using a proprietary technique. The tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The monkey (Cynomolgus) brain tissue membrane is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, Sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the brain tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot. |
Brain Membrane Lysate |
21-241 |
ProSci |
0.1 mg |
EUR 516.5 |
Description: Monkey (Rhesus) brain tissue membrane protein lysate was prepared by homogenization using a proprietary technique. The tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The monkey (Rhesus) brain tissue membrane is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, Sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the brain tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot. |
Heart Membrane Lysate |
21-243 |
ProSci |
0.1 mg |
EUR 516.5 |
Description: Monkey (Rhesus) heart tissue membrane protein lysate was prepared by homogenization using a proprietary technique. The tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The monkey (Rhesus) heart tissue membrane is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, Sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the heart tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated heart tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot. |
Brain Membrane Lysate |
21-358 |
ProSci |
0.1 mg |
EUR 516.5 |
Description: Mouse brain tissue membrane protein lysate was prepared by homogenization using a proprietary technique. The tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The mouse brain tissue membrane is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, Sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the brain tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot. |
Brain Membrane Lysate |
21-440 |
ProSci |
0.1 mg |
EUR 516.5 |
Description: Rat brain tissue membrane protein lysate was prepared by homogenization using a proprietary technique. The tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The rat brain tissue membrane is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, Sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the brain tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot. |
Brain Membrane Lysate |
XBL-10166 |
ProSci |
0.1 mg |
EUR 516.5 |
Description: Human brain tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human brain tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated brain tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
Hippocampus Membrane Lysate |
XBL-10180 |
ProSci |
0.1 mg |
EUR 852.5 |
Description: Human brain hippocamps tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human hippocamps tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated brain hippocamps tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain hippocamps tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
Thalamus Membrane Lysate |
XBL-10204 |
ProSci |
0.1 mg |
EUR 516.5 |
Description: Human brain thalamus tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human thalamus tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated brain thalamus tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain thalamus tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
Amygdala Membrane Lysate |
XBL-10237 |
ProSci |
0.1 mg |
EUR 737 |
Description: Human brain amygdala tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human amygdala tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated brain amygdala tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain amygdala tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
Pituitary Membrane Lysate |
XBL-10263 |
ProSci |
0.1 mg |
EUR 989 |
Description: Human brain pituitary tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human pituitary tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated brain pituitary tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated brain pituitary tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
A431 Membrane Lysate |
XBL-10438 |
ProSci |
0.1 mg |
EUR 516.5 |
Description: A431 (Human Epidermoid Carcinoma) cell membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The A431 (Human Epidermoid Carcinoma) cell was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated A431 (Human Epidermoid Carcinoma) cell membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated A431 (Human Epidermoid Carcinoma) cell membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
HeLa Membrane Lysate |
XBL-10439 |
ProSci |
0.1 mg |
EUR 516.5 |
Description: Hela (Human cervix Adenocarcinoma) cell membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The Hela (Human cervix Adenocarcinoma) cell was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated Hela (cervix Adenocarcinoma) cell membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated Hela (cervix Adenocarcinoma) cell membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
Jurkat Membrane Lysate |
XBL-10440 |
ProSci |
0.1 mg |
EUR 516.5 |
Description: Jurkat (Human Acute T cell Leukemia) cell membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The Jurkat (Human Acute T cell Leukemia) cell was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated Jurkat (Human Acute T cell Leukemia) cell membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated Jurkat (Human Acute T cell Leukemia) cell membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
K562 Membrane Lysate |
XBL-10441 |
ProSci |
0.1 mg |
EUR 516.5 |
Description: K562 (Human Chronic Myelogenous Leukemia; Bone Marrow) cell membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The K562 (Human Chronic Myelogenous Leukemia; Bone Marrow) cell was frozen in liquid nitrogen immediately after excision and then stored at -70ºC. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated K562 (Human Chronic Myelogenous Leukemia; Bone Marrow) cell membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated K562 (Human Chronic Myelogenous Leukemia; Bone Marrow) cell membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
Raji Membrane Lysate |
XBL-10443 |
ProSci |
0.1 mg |
EUR 516.5 |
Description: Raji (Human lymphoma; B lymphoma) cell membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The Raji (Human lymphoma; B lymphoma) cell was frozen in liquid nitrogen immediately after excision and then stored at -70ºC. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated Raji (Human lymphoma; B lymphoma) cell membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated Raji (Human lymphoma; B lymphoma) cell membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
In specific, perovskite single crystals have emerged as promising candidates for ionization radiation detection, because of the wonderful opto-electronic properties. However, a lot of the reported crystals are grown in natural solvents and require excessive temperature. In this work, we develop a low-temperature crystallization technique to develop CsPbBr3 perovskite single crystals in water. Then, we fastidiously examine the construction and optoelectronic properties of the crystals obtained, and evaluate them with CsPbBr3 crystals grown in dimethyl sulfoxide. Interestingly, the water grown crystals exhibit a distinct crystal behavior, superior cost transport properties and higher stability in air.