MOCS1 antibody (AA 52-84)

Catalog No. ABIN7875572

This Rabbit Polyclonal antibody specifically detects MOCS1 in WB, ELISA, IHC (p), IF and FACS. It exhibits reactivity toward Human, Mouse and Rat.

Quick Overview for MOCS1 antibody (AA 52-84) (ABIN7875572)

Target: MOCS1 (Molybdenum Cofactor Synthesis 1 (MOCS1))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MOCS1 antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF), Flow Cytometry (FACS)

Product Details anti-MOCS1 Antibody

Binding Specificity: AA 52-84

Purpose: MOCS1 Antibody / Molybdenum cofactor biosynthesis protein 1

Purification: Antigen affinity purified

Immunogen: An E.coli-derived human recombinant protein (E52-R84) was used as the immunogen for the MOCS1 antibody.

Isotype: IgG

Application Details

Application Notes: Optimal dilution of the MOCS1 antibody should be determined by the researcher.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Storage: 4 °C,-20 °C

Storage Comment: After reconstitution, the MOCS1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Target Details for MOCS1

Target: MOCS1 (Molybdenum Cofactor Synthesis 1 (MOCS1))

Alternative Name: MOCS1

Background: Molybdenum cofactor biosynthesis protein 1 is a protein that in humans and other animals, fungi, and cellular slime molds, is encoded by the MOCS1 gene. Molybdenum cofactor biosynthesis is a conserved pathway leading to the biological activation of molybdenum. The protein encoded by this gene is involved in this pathway. This gene was originally thought to produce a bicistronic mRNA with the potential to produce two proteins (MOCS1A and MOCS1B) from adjacent open reading frames. However, only the first open reading frame (MOCS1A) has been found to encode a protein from the putative bicistronic mRNA, whereas additional splice variants are likely to produce a fusion between the two open reading frames. This gene is defective in patients with molybdenum cofactor deficiency, type A. A related pseudogene has been identified on chromosome 16.

UniProt: Q9NZB8