China Good Wholesale Vendors Oncology Drugs - Glutathione reduced Cas: 70-18-8 98-101% Clear and colourless – XD BIOCHEM Manufacturer and Supplier

Good Wholesale Vendors Oncology Drugs - Glutathione reduced Cas: 70-18-8 98-101% Clear and colourless – XD BIOCHEM

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Good Wholesale Vendors Oncology Drugs - Glutathione reduced Cas: 70-18-8 98-101% Clear and colourless – XD BIOCHEM Detail:

Catalog Number	XD90284
Product Name	Glutathione reduced
CAS	70-18-8
Molecular Formula	C10H17N3O6S
Molecular Weight	307.32
Storage Details	2 to 8 °C
Harmonized Tariff Code	29309098

Product Specification

Assay	98% – 101%
Appearance	White crystalline powder
Grade	EP 7.0
Impurity A	<0.5%
Impurity B	<0.5%
Heavy metals	<10ppm
Bacterial endotoxin	<0.10EU/mg
Impurity C	<1.5%
Impurity D	<1.0%
Loss on Drying	<0.5%
Solubility	Freely soluble in water, slightly soluble in ethanol and methylene chloride
Iron	<10ppm
Chlorides	<200ppm
Appearance of Solution	Clear and colourless
Specific optical rotation	-15.5 to -17.5
Total Impurities	<2.5%
Ammonium	<200ppm
Sulfated ash	<0.1%
Sulphates	<300ppm
Impurity E	<0.5%

Post-translational protein modifications, such as tyrosine phosphorylation, regulate protein-protein interactions (PPIs) critical for signal processing and cellular phenotypes. We extended an established yeast two-hybrid system employing human protein kinases for the analyses of phospho-tyrosine (pY)-dependent PPIs in a direct experimental, large-scale approach. We identified 292 mostly novel pY-dependent PPIs which showed high specificity with respect to kinases and interacting proteins and validated a large fraction in co-immunoprecipitation experiments from mammalian cells. About one-sixth of the interactions are mediated by known linear sequence binding motifs while the majority of pY-PPIs are mediated by other linear epitopes or governed by alternative recognition modes. Network analysis revealed that pY-mediated recognition events are tied to a highly connected protein module dedicated to signaling and cell growth pathways related to cancer. Using binding assays, protein compleme ntation and phenotypic readouts to characterize the pY-dependent interactions of TSPAN2 (tetraspanin 2) and GRB2 or PIK3R3 (p55γ), we exemplarily provide evidence that the two pY-dependent PPIs dictate cellular cancer phenotypes.

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