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CHSTB Polyclonal Antibody, 50ul Miscellaneous a disorder characterized by urinary

SKU: 13018208348

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CHSTB Polyclonal Antibody, 50ul Miscellaneous a disorder characterized by urinaryThe protein encoded by this gene belongs to the sulfotransferase 2 family. It is localized to the golgi membrane, and catalyzes the transfer of sulfate to position 4 of the N acetylgalactosamine (GalNAc) residue of chondroitin. Chondroitin sulfate constitutes the predominant proteoglycan present in cartilage, and is distributed on the surfaces of many cells and extracellular matrices. A chromosomal translocation involving this gene and IgH, t(12;

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Description

a disorder characterized by urinary salt wasting

mismatch repair system component forms heterodimers with the gene product of the mutL homolog 1 (MLH1) gene to form the MutL-alpha heterodimer

The active protein is a homodimer that binds to the interferon gamma receptor which triggers a cellular response to viral and microbial infections

Mutations in this gene may be associated with a range of autoimmune disorders including Type 1 Diabetes

displaying diverse cytoplasm-to-nucleus trafficking patterns and distinct transcriptional activities (PMID: 15866175)

CHSTB Polyclonal Antibody, 50ul Miscellaneous a disorder characterized by urinaryThe protein encoded by this gene belongs to the sulfotransferase 2 family. It is localized to the golgi membrane, and catalyzes the transfer of sulfate to position 4 of the N acetylgalactosamine (GalNAc) residue of chondroitin. Chondroitin sulfate constitutes the predominant proteoglycan present in cartilage, and is distributed on the surfaces of many cells and extracellular matrices. A chromosomal translocation involving this gene and IgH, t(12;

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