HMGB3 rabbit pAb
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HMGB3 rabbit pAb
Background :
This gene encodes a member of a family of proteins containing one or more high mobility group DNA-binding motifs. The encoded protein plays an important role in maintaining stem cell populations, and may be aberrantly expressed in tumor cells. A mutation in this gene was associated with microphthalmia, syndromic 13. There are numerous pseudogenes of this gene on multiple chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]Description :
This gene encodes a member of a family of proteins containing one or more high mobility group DNA-binding motifs. The encoded protein plays an important role in maintaining stem cell populations, and may be aberrantly expressed in tumor cells. A mutation in this gene was associated with microphthalmia, syndromic 13. There are numerous pseudogenes of this gene on multiple chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014],UniProt :
O15347Swiss Prot :
O15347Reactivity :
Human; MouseImmunogen :
Synthesized peptide derived from human HMGB3 AA range: 123-173Target :
HMGB3Clonality :
PolyclonalSource :
RabbitApplications :
WBConcentration :
1 mg/mlDilution :
WB 1:500-2000Buffer :
-20°C/1 yearStorage Conditions :
-20°C/1 yearFragment :
IgGSubcellular Location :
Nucleus . Chromosome . Cytoplasm .Gene ID (Human) :
3149

