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Rabbit monoclonal [EPR8695] to MMAB
ICC/IF more details Unsuitable for:
Flow Cyt,IHC-P or IP
Rat, Human Does not react with:
Synthetic peptide within Human MMAB aa 1-100 (Cysteine residue). The exact sequence is proprietary.
Database link: Q96EY8
HepG2, A673 and Human fetal liver lysates; HepG2 cells.
® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMab ® patents
This product is a recombinant rabbit monoclonal antibody.
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C. Avoid freeze / thaw cycle.
Preservative: 0.01% Sodium azide Constituents: 9% PBS, 40% Glycerol, 0.05% BSA, 50% Tissue culture supernatant
Tissue culture supernatant
Abpromise guarantee covers the use of
in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
1/1000 - 1/10000. Predicted molecular weight: 27 kDa.
1/50 - 1/100.
Is unsuitable for Flow Cyt,IHC-P or IP.
Expressed in liver and skeletal muscle.
Cofactor biosynthesis; adenosylcobalamin biosynthesis; adenosylcobalamin from cob(II)yrinate a,c-diamide: step 2/7.
Involvement in disease
Defects in MMAB are the cause of methylmalonic aciduria type cblB (MMAB) [MIM:251110]; also known as methylmalonic aciduria type B or vitamin B12-responsive methylmalonicaciduria of cblB complementation type. MMAB is a disorder of methylmalonate and cobalamin metabolism due to defective synthesis of adenosylcobalamin. Inheritance is autosomal recessive.
Belongs to the Cob(I)alamin adenosyltransferase family.
Information by UniProt
aquocob(I)alamin vitamin B12s adenosyltransferase antibody
ATP:cob(I)alamin adenosyltransferase antibody
ATP:corrinoid adenosyltransferase antibody
has not yet been referenced specifically in any publications.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"