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Rabbit Anti-MOCS2 Antibody (CSB-PA014706ESR1HU)
Supplier: CUSABIO BIOTECH CO.
Molybdopterin synthase sulfur carrier subunit Antibody,MOCO1-A Antibody,Molybdenum cofactor synthesis protein 2 small subunit Antibody,MOCS2 Antibody,MOCO1 AntibodyMore alternative names for the antibody
MCBPE antibody|MOCO1 antibody|MOCO1 B antibody|MOCO1B antibody|MOCS 2 antibody|MOCS2 antibody|MOCS2A antibody|MOCS2B antibody|Molybdenum cofactor biosynthesis protein E antibody|Molybdenum cofactor synthesis 2 antibody|Molybdenum cofactor synthesis protein 2 large subunit antibody|molybdenum cofactor synthesis protein 2 small subunit antibody|molybdenum cofactor synthesis protein 2A antibody|Molybdenum cofactor synthesis protein 2B antibody|Molybdopterin synthase antibody|Molybdopterin synthase large subunit antibody|molybdopterin-synthase small subunit antibody|MPT synthase antibody|MPTS antibody|OTTHUMP00000122459 antibody|sulfur carrier protein MOCS2A antibody
Anti-MOCS2 antibody (ab122406)
Anti-MOCS2 antibody (ab122406)
Recommended applications: ELISA, WB, IHC, IP
Recommended dilution: Recommended dilution:WB:1:1000-1:5000,IHC:1:20-1:200,IP:1:200-1:2000
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Molybdopterin synthase sulfur carrier subunit protein (1-188AA)
ELISA, WB, IHC, IP
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Protein function|| |
Catalytic subunit of the molybdopterin synthase complex, a complex that catalyzes the conversion of precursor Z into molybdopterin. Acts by mediating the incorporation of 2 sulfur atoms from thiocarboxylated MOCS2A into precursor Z to generate a dithiolene group. .
|Protein tissue specificity|| |
Highest levels are found in heart and skeletal muscle. Lower levels are present in brain, kidney and pancreas. Very low levels are found in lung and peripheral blood leukocytes. .
|Involvement in disease|| |
Molybdenum cofactor deficiency, complementation group B (MOCODB) [MIM:252160]: An autosomal recessive metabolic disorder characterized by neonatal onset of intractable seizures, opisthotonus, and facial dysmorphism associated with hypouricemia and elevated urinary sulfite levels. Affected individuals show severe neurologic damage and often die in early childhood. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the MoaE family. MOCS2B subfamily.
|Protein cellular localization|| |
Cytoplasm, cytosol .
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CUSABIO BIOTECH CO.
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