MMAA purified MaxPab mouse polyclonal antibody (B03P)
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More Files
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Specification
Product Description
Mouse polyclonal antibody raised against a full-length human MMAA protein.
Immunogen
MMAA (NP_758454.1, 1 a.a. ~ 418 a.a) full-length human protein.
Sequence
MPMLLPHPHQHFLKGLLRAPFRCYHFIFHSSTHLGSGIPCAQPFNSLGLHCTKWMLLSDGLKRKLCVQTTLKDHTEGLSDKEQRFVDKLYTGLIQGQRACLAEAITLVESTHSRKKELAQVLLQKVLLYHREQEQSNKGKPLAFRVGLSGPPGAGKSTFIEYFGKMLTERGHKLSVLAVDPSSCTSGGSLLGDKTRMTELSRDMNAYIRPSPTRGTLGGVTRTTNEAILLCEGAGYDIILIETVGVGQSEFAVADMVDMFVLLLPPAGGDELQGIKRGIIEMADLVAVTKSDGDLIVPARRIQAEYVSALKLLRKRSQVWKPKVIRISARSGEGISEMWDKMKDFQDLMLASGELTAKRRKQQKVWMWNLIQESVLEHFRTHPTVREQIPLLEQKVLIGALSPGLAADFLLKAFKSRD
Host
Mouse
Reactivity
Human
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Transfected lysate)
Western Blot analysis of MMAA expression in transfected 293T cell line (H00166785-T02) by MMAA MaxPab polyclonal antibody.
Lane 1: MMAA transfected lysate(45.98 KDa).
Lane 2: Non-transfected lysate.
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Gene Info — MMAA
Entrez GeneID
166785GeneBank Accession#
NM_172250Protein Accession#
NP_758454.1Gene Name
MMAA
Gene Alias
MGC120010, MGC120011, MGC120012, MGC120013
Gene Description
methylmalonic aciduria (cobalamin deficiency) cblA type
Gene Ontology
HyperlinkGene Summary
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. [provided by RefSeq
Other Designations
methylmalonic aciduria type A
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