MCCC2 purified MaxPab rabbit polyclonal antibody (D01P)
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More Files
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Specification
Product Description
Rabbit polyclonal antibody raised against a full-length human MCCC2 protein.
Immunogen
MCCC2 (NP_071415.1, 1 a.a. ~ 563 a.a) full-length human protein.
Sequence
MWAVLRLALRPCARASPAGPRAYHGDSVASLGTQPDLGSALYQENYKQMKALVNQLHERVEHIKLGGGEKARALHISRGKLLPRERIDNLIDPGSPFLELSQFAGYQLYDNEEVPGGGIITGIGRVSGVECMIIANDATVKGGAYYPVTVKKQLRAQEIAMQNRLPCIYLVDSGGAYLPRQADVFPDRDHFGRTFYNQAIMSSKNIAQIAVVMGSCTAGGAYVPAMADENIIVRKQGTIFLAGPPLVKAATGEEVSAEDLGGADLHCRKSGVSDHWALDDHHALHLTRKVVRNLNYQKKLDVTIEPSEEPLFPADELYGIVGANLKRSFDVREVIARIVDGSRFTEFKAFYGDTLVTGFARIFGYPVGIVGNNGVLFSESAKKGTHFVQLCCQRNIPLLFLQNITGFMVGREYEAEGIAKDGAKMVAAVACAQVPKITLIIGGSYGAGNYGMCGRAYSPRFLYIWPNARISVMGGEQAANVLATITKDQRAREGKQFSSADEAALKEPIIKKFEEEGNPYYSSARVWDDGIIDPADTRLVLGLSFSAALNAPIEKTDFGIFRM
Host
Rabbit
Reactivity
Human, Mouse
Interspecies Antigen Sequence
Mouse (88); Rat (88)
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 (Tissue lysate)
MCCC2 MaxPab rabbit polyclonal antibody. Western Blot analysis of MCCC2 expression in human colon.Western Blot (Tissue lysate)
MCCC2 MaxPab rabbit polyclonal antibody. Western Blot analysis of MCCC2 expression in mouse lung.Western Blot (Cell lysate)
MCCC2 MaxPab rabbit polyclonal antibody. Western Blot analysis of MCCC2 expression in HepG2.Western Blot (Transfected lysate)
Western Blot analysis of MCCC2 expression in transfected 293T cell line (H00064087-T01) by MCCC2 MaxPab polyclonal antibody.
Lane 1: MCCC2 transfected lysate(61.30 KDa).
Lane 2: Non-transfected lysate.
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Gene Info — MCCC2
Entrez GeneID
64087GeneBank Accession#
NM_022132.3Protein Accession#
NP_071415.1Gene Name
MCCC2
Gene Alias
MCCB
Gene Description
methylcrotonoyl-Coenzyme A carboxylase 2 (beta)
Gene Ontology
HyperlinkGene Summary
This gene encodes the small subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA. Mutations in this gene are associated with 3-Methylcrotonylglycinuria, an autosomal recessive disorder of leucine catabolism. [provided by RefSeq
Other Designations
biotin carboxylase|non-biotin containing subunit of 3-methylcrotonyl-CoA carboxylase
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Interactome
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Pathway
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Disease
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