Further Information
IFT122, SPG, WDR10, WDR10p, WDR140, CED, CED1
IFT122 antibody can be used for detection of IFT122 by ELISA at 1:1562500. IFT122 antibody can be used for detection of IFT122 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
IFT122 is a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. IFT122 contains seven WD repeats and an AF-2 domain which function by recruiting coregulatory molecules and in transcriptional activation.This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This cytoplasmic protein contains seven WD repeats and an AF-2 domain which function by recruiting coregulatory molecules and in transcriptional activation. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
- Gross, C., (2001) DNA Cell Biol. 20 (1), 41-52.
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
batch dependent
Unconjugated
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human IFT122.
55764
intraflagellar transport 122 homolog (Chlamydomonas)
IFT122
Homo sapiens
Liquid
PREDICTED MOLECULAR WEIGHT:
129 kDa
NP_443716
16554625
Antibody is purified by peptide affinity chromatography method.
Q9HBG6
Optimal dilutions for each application to be determined by the researcher.