MGST2 (GeneName), Microsomal glutathione S-transferase 2 (ProteinName), MGST2_BOVIN.
Bovine MGST2/ Microsomal glutathione S-transferase 2 ELISA Kit
Natural and recombinant bovine Microsomal glutathione S-transferase 2
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Can catalyze the production of LTC4 from LTA4 and reduced glutathione. Can catalyze the conjugation of 1-chloro-2,4-dinitrobenzene with reduced glutathione.
Endoplasmic reticulum membrane Multi-pass membrane protein Microsome membrane Multi-pass membrane protein
MAGNSILLAA | LSVLSACQQS | YFAMQVGKAR | SKYKVTPPSV | SGSPDFERIF |
RAQQNCVEFY | PIFIITLWMA | GWYFNQVFAT | CLGLVYIYSR | HQYFWGYAEA |
AKKRVTGFRL | SLGVLALLTV | LGAVGILNSF | LDEYLDIDIA | KKLRHF
This product has not yet been referenced specifically in any publications.
"A novel MGST2 non-synonymous mutation in a Chinese pedigree with psoriasis vulgaris."
"Systematic evaluation of association between the microsomal glutathione S-transferase 2 common variation and psoriasis vulgaris in Chinese population."
"Identification and characterization of a novel human microsomal glutathione S-transferase with leukotriene C4 synthase activity and significant sequence identity to 5-lipoxygenase-activating protein and leukotriene C4 synthase."
"Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score."
"Association study between single-nucleotide polymorphisms in 199 drug-related genes and commonly measured quantitative traits of 752 healthy Japanese subjects."
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
"Human umbilical vein endothelial cells generate leukotriene C4 via microsomal glutathione S-transferase type 2 and express the CysLT(1) receptor."
"Architecture of the human interactome defines protein communities and disease networks."
"Global mapping of herpesvirus-host protein complexes reveals a transcription strategy for late genes."
"Widespread macromolecular interaction perturbations in human genetic disorders."
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