MMAB antibody

Catalog No. ABIN2726116

The Mouse Monoclonal anti-MMAB antibody is suitable to detect MMAB in samples from Human. It has been validated for WB, FACS and IF.

Quick Overview for MMAB antibody (ABIN2726116)

Target: MMAB (Methylmalonic Aciduria (Cobalamin Deficiency) CblB Type (MMAB))

Reactivity: Human

Host: Mouse

Clonality: Monoclonal

Conjugate: This MMAB antibody is un-conjugated

Application: Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (IF)

Clone: 4D12

Product Details anti-MMAB Antibody

Characteristics: Homo sapiens methylmalonic aciduria (cobalamin deficiency) cblB type (MMAB), nuclear gene encoding mitochondrial protein, transcript variant 1

Purification: Purified from mouse ascites fluids by affinity chromatography

Immunogen: Full length human recombinant protein of human MMAB (NP_443077) produced in HEK293T cell.

Isotype: IgG2a

Application Details

Application Notes: WB 1:2000, IF 1:100, FLOW 1:100

Comment:

The concentration of the product may vary between diferrent lots.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.5-1.0 mg/mL

Buffer: PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % 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: -20 °C

Target Details for MMAB

Target: MMAB (Methylmalonic Aciduria (Cobalamin Deficiency) CblB Type (MMAB))

Alternative Name: MMAB

Background: This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group.

Molecular Weight: 24 kDa

Gene ID: 326625

NCBI Accession: NM_052845

HGNC: 326625