UBAP1 rabbit pAb
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UBAP1 rabbit pAb
Background :
This gene is a member of the UBA domain family, whose members include proteins having connections to ubiquitin and the ubiquitination pathway. The ubiquitin associated domain is thought to be a non-covalent ubiquitin binding domain consisting of a compact three helix bundle. This particular protein originates from a gene locus in a refined region on chromosome 9 undergoing loss of heterozygosity in nasopharyngeal carcinoma (NPC) . Taking into account its cytogenetic location, this UBA domain family member is being studies as a putative target for mutation in nasopharyngeal carcinomas. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]Description :
This gene is a member of the UBA domain family, whose members include proteins having connections to ubiquitin and the ubiquitination pathway. The ubiquitin associated domain is thought to be a non-covalent ubiquitin binding domain consisting of a compact three helix bundle. This particular protein originates from a gene locus in a refined region on chromosome 9 undergoing loss of heterozygosity in nasopharyngeal carcinoma (NPC). Taking into account its cytogenetic location, this UBA domain family member is being studies as a putative target for mutation in nasopharyngeal carcinomas. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010],UniProt :
Q9NZ09Swiss Prot :
Q9NZ09Reactivity :
Human; Rat; MouseImmunogen :
Synthesized peptide derived from part region of human proteinClonality :
PolyclonalSource :
RabbitApplications :
WB; ELISAConcentration :
1 mg/mlDilution :
WB 1:500-2000 ELISA 1:5000-20000Molecular Weight :
55kDStorage Conditions :
-20°C/1 yearObserved Molecular Weight :
55kDFragment :
IgGSubcellular Location :
Cytoplasm, cytosol . Endosome . Predominantly cytosolic (PubMed:21757351) . Recruited to endosomes as part of the ESCRT-I complex (PubMed:21757351) . .Gene ID (Human) :
51271

