MMAA Antibody

Product Specifications

Background

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.

NCBI Gene ID

166785

Swiss Prot

Q8IVH4

Accession Number

Q8IVH4

Host

Rabbit

Reactivity

Human, Mouse

Immunogen

This MMAA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 56-84 amino acids from the N-terminal region of human MMAA.

Clonality

Polyclonal

Conjugation

Unconjugated

Type

Primary Antibodies

Field of Research

Obesity, Signal Transduction

Purification

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

Concentration

Batch dependent

Buffer

Supplied in PBS with 0.09% (W/V) sodium azide.

Modification

None

Shipping Conditions

Blue Ice

Storage Conditions

Store at 4˚ C for three months and -20˚ C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Calculated Molecular Weight

47 kDa

Fragment

Rabbit Ig

Symbol

MMAA

NCBI Official Name

Methylmalonic aciduria type A protein, mitochondrial

NCBI Organism

Homo sapiens

Background Reference 01

Honjo, R.S., et al. Genet Test Mol Biomarkers 13 (2) :181-183 (2009)

Background Reference 02

Merinero, B., et al. J. Inherit. Metab. Dis. 31 (1) :55-66 (2008)

Background Reference 03

Horster, F., et al. Pediatr. Res. 62 (2) :225-230 (2007)

Background Reference 04

Padovani, D., et al. J. Biol. Chem. 281 (26) :17838-17844 (2006)

Other Product Names

Methylmalonic aciduria type A protein, mitochondrial, 36--, MMAA

Tested Applications

WB, IHC-P

Protein ID

38258173

Physical Properties

Liquid

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