MMAB DNAxPab
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More Files
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Specification
Product Description
Rabbit polyclonal antibody raised against a full-length human MMAB DNA using DNAx™ Immune technology.
Technology
Immunogen
Full-length human DNA
Sequence
MAVCGLGSRLGLGSRLGLRGCFGAARLLYPRFQSRGPQGVEDGDRPQPSSKTPRIPKIYTKTGDKGFSSTFTGERRPKDDQVFEAVGTTDELSSAIGFALELVTEKGHTFAEELQKIQCTLQDVGSALATPCSSAREAHLKYTTFKAGPILELEQWIDKYTSQLPPLTAFILPSGGKISSALHFCRAVCRRAERRVVPLVQMGETDANVAKFLNRLSDYLFTLARYAAMKEGNQEKIYMKNDPSAESEGL
Host
Rabbit
Reactivity
Human
Purification
Protein A
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)
Immunofluorescence (Transfected cell)
Flow Cytometry (Transfected cell)
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Gene Info — MMAB
Entrez GeneID
326625GeneBank Accession#
NM_052845.2Protein Accession#
NP_443077.1Gene Name
MMAB
Gene Alias
ATR, MGC20496
Gene Description
methylmalonic aciduria (cobalamin deficiency) cblB type
Gene Ontology
HyperlinkGene Summary
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. [provided by RefSeq
Other Designations
ATP:cob(I)alamin adenosyltransferase|ATP:corrinoid adenosyltransferase|aquocob(I)alamin vitamin B12s adenosyltransferase|cob(I)alamin adenosyltransferase|cob(I)yrinic acid a,c-diamide adenosyltransferase|methylmalonic aciduria type B protein
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Interactome
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Pathway
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Disease
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