Recombinant Human POMT1, GST-tagged
Cat.No. : | POMT1-1856H |
Product Overview : | Recombinant Human POMT1 protein, fused to GST-tag, was expressed in E.coli and purified by GSH-sepharose. |
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Source : | E.coli |
Species : | Human |
Tag : | GST |
Protein length : | 285-595aa |
Storage : | The protein is stored in PBS buffer at -20℃. Avoid repeated freezing and thawing cycles. |
Storage Buffer : | 1M PBS (58mM Na2HPO4,17mM NaH2PO4, 68mM NaCl, pH8. ) added with 100mM GSH and 1% Triton X-100,15%glycerol. |
Gene Name : | POMT1?protein-O-mannosyltransferase 1 [?Homo sapiens?(human) ] |
Official Symbol : | POMT1 |
Synonyms : | POMT1; RT; LGMD2K; MDDGA1; MDDGB1; MDDGC1; protein-O-mannosyltransferase 1; protein O-mannosyl-transferase 1; dolichyl-phosphate-mannose-protein mannosyltransferase; dolichyl-phosphate-mannose--protein mannosyltransferase 1; NP_001070833.1; EC 2.4.1.109; NP_001070834.1; NP_001129585.1; NP_009102.3 |
Gene ID : | 10585 |
mRNA Refseq : | NM_001077365 |
Protein Refseq : | NP_001070833 |
MIM : | 607423 |
UniProt ID : | Q9Y6A1 |
Chromosome Location : | 9q34.1 |
Pathway : | Other types of O-glycan biosynthesis |
Function : | dolichyl-phosphate-mannose-protein mannosyltransferase activity; mannosyltransferase activity; metal ion binding |
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For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
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Q&As (7)
Ask a questionGenetic defects in POMT1 can lead to impaired muscle development and function, contributing to muscular dystrophies.
Targeting POMT1 in therapy could provide new treatments for various forms of muscular dystrophy.
Altered POMT1 activity impacts the stability and function of muscle proteins, exacerbating neuromuscular diseases.
POMT1 plays a role in maintaining cell membrane integrity, crucial for muscle and nerve cells.
POMT1 works with other glycosylation enzymes, playing a critical role in protein modification processes.
POMT1 is involved in the O-mannosylation of proteins, an important type of glycosylation for protein function.
Mutations in POMT1 are linked to certain types of muscular dystrophies, affecting muscle structure and function.
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