GTD2A rabbit pAb
This gene is one of several closely related genes on chromosome 7 encoding proteins containing helix-loop-helix motifs. These proteins may function as regulators of transcription. The encoded protein is unique in that its C-terminus is derived from CHARLIE8 transposable element sequence. This gene is located in a region of chromosome 7 that is deleted in Williams-Beuren syndrome, and loss of this locus may contribute to the cognitive phenotypes observed in this disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013],
Product Specifications
Background
Product Name Alternative
UniProt
Q86UP8
Swiss Prot
Q86UP8
Reactivity
Human; Rat; Mouse
Immunogen
Synthesized peptide derived from human GTD2A AA range: 529-579
Target
GTD2A
Clonality
Polyclonal
Source
Rabbit
Applications
WB
Concentration
1 mg/ml
Dilution
WB 1:500-2000
Buffer
-20°C/1 year
Molecular Weight
105kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
105kD
Fragment
IgG
Subcellular Location
Nucleus.
Other Product Names
Gene ID (Human)
84163
Available Sizes
Explore Other Products
Discover premium biology products from our extensive collection of 20M+ items