CHD2 rabbit pAb
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CHD2 rabbit pAb
Background:
The CHD family of proteins is characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. CHD genes alter gene expression possibly by modification of chromatin structure thus altering access of the transcriptional apparatus to its chromosomal DNA template. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]Description:
The CHD family of proteins is characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. CHD genes alter gene expression possibly by modification of chromatin structure thus altering access of the transcriptional apparatus to its chromosomal DNA template. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008],UniProt:
O14647Swiss Prot:
O14647Reactivity:
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:
201kDStorage Conditions:
-20°C/1 yearObserved Molecular Weight:
201kDFragment:
IgGSubcellular Location:
Nucleus . Binds to myogenic gene promoters. .Gene ID (Human):
1106
