CHD7 rabbit pAb
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CHD7 rabbit pAb
Background:
This gene encodes a protein that contains several helicase family domains. Mutations in this gene have been found in some patients with the CHARGE syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]Description:
This gene encodes a protein that contains several helicase family domains. Mutations in this gene have been found in some patients with the CHARGE syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015],UniProt:
Q9P2D1Swiss Prot:
Q9P2D1Reactivity:
Human; MouseImmunogen:
Synthesized peptide derived from human CHD7 AA range: 1703-1753Clonality:
PolyclonalSource:
RabbitApplications:
IHC; IFConcentration:
1 mg/mlDilution:
IHC-p 1: 50-200Storage Conditions:
-20°C/1 yearFragment:
IgGSubcellular Location:
[Isoform 1]: Nucleus .; [Isoform 3]: Nucleus, nucleolus .Gene ID (Human):
55636
