MOCS1 antibody (N-Term)

Catalog No. ABIN1539287

The Rabbit Polyclonal anti-MOCS1 antibody has been validated for WB. It is suitable to detect MOCS1 in samples from Human.

Quick Overview for MOCS1 antibody (N-Term) (ABIN1539287)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MOCS1 antibody is un-conjugated

Application: Western Blotting (WB)

Clone: RB38897

Product Details anti-MOCS1 Antibody

Binding Specificity: AA 31-58, N-Term

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This MOCS1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 31-58 amino acids from the N-terminal region of human MOCS1.

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: MOCS1 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Expiry Date: 6 months

Target Details for MOCS1

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

Alternative Name: MOCS1

Background: 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, whose full-length natures have yet to be determined, 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.

Molecular Weight: 70105

Gene ID: 4337

NCBI Accession: NP_001068566, NP_005934

UniProt: Q9NZB8