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cblA Rabbit anti-Human, Polyclonal, Bioss
SDP

Catalog No. 501989488
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100 μL
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50-198-9488 100 μL
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Catalog No. 50-198-9488 Supplier Bioss Supplier No. BS9961R
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Rabbit Polyclonal Antibody

The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria.

Specifications

Antigen cblA
Applications Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot
Classification Polyclonal
Concentration 1 μg/mL
Conjugate Unconjugated
Formulation PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH
Gene MMAA
Gene Accession No. Q8IVH4
Gene Alias cblA; methylmalonic aciduria (cobalamin deficiency) cblA type; Methylmalonic aciduria type A protein, mitochondrial; MMAA; mutant adenosylcobalamin
Gene Symbols MMAA
Host Species Rabbit
Immunogen KLH conjugated synthetic peptide derived from human MMAA/cblA.
Purification Method Protein A
Quantity 100 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 166785
Target Species Human
Content And Storage -20°C
Product Type Antibody
Form Liquid
Isotype IgG
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