ARG55862

anti-MMAB antibody

anti-MMAB antibody for Western blot and Human

Overview

Product Description Rabbit Polyclonal antibody recognizes MMAB
Tested Reactivity Hu
Predict Reactivity Ms
Tested Application WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name MMAB
Antigen Species Human
Immunogen KLH-conjugated synthetic peptide corresponding to aa. 50-81 (Center) of Human MMAB.
Conjugation Un-conjugated
Alternate Names ATR; cob; cblB; CFAP23; Cob(I)yrinic acid a,c-diamide adenosyltransferase, mitochondrial; EC 2.5.1.17; Cob(I)alamin adenosyltransferase; Methylmalonic aciduria type B protein

Application Instructions

Application Suggestion
Tested Application Dilution
WB1:1000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Positive Control HepG2

Properties

Form Liquid
Purification Purification with Protein A and immunogen peptide.
Buffer PBS and 0.09% (W/V) Sodium azide
Preservative 0.09% (W/V) Sodium azide
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 326625 Human MMAB

Swiss-port # Q96EY8 Human Cob(I)yrinic acid a,c-diamide adenosyltransferase, mitochondrial

Gene Symbol MMAB
Gene Full Name methylmalonic aciduria (cobalamin deficiency) cblB type
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. Alternatively spliced transcript variants have been found. [provided by RefSeq, Apr 2011]
Cellular Localization Mitochondrion.
Calculated MW 27 kDa