
Western blot analysis of human RAD17 in heart lysate with anti-huRAD17 (GTX30134) at a 1:500 dilution.
Rad17 antibody
GTX30134
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry
Product group Antibodies
ReactivityHuman
TargetRAD17
Overview
- SupplierGeneTex
- Product NameRad17 antibody
- Delivery Days Customer9
- ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry
- CertificationResearch Use Only
- ClonalityPolyclonal
- Concentration1 mg/ml
- ConjugateUnconjugated
- Gene ID5884
- Target nameRAD17
- Target descriptionRAD17 checkpoint clamp loader component
- Target synonymsCCYC, HRAD17, R24L, RAD17SP, RAD24, cell cycle checkpoint protein RAD17, RAD1 homolog, RAD17 homolog, RF-C activator 1 homolog, Rad17-like protein, cell cycle checkpoint protein (RAD17)
- HostRabbit
- IsotypeIgG
- Protein IDO75943
- Protein NameCell cycle checkpoint protein RAD17
- Scientific DescriptionThe protein encoded by this gene is highly similar to the gene product of Schizosaccharomyces pombe rad17, a cell cycle checkpoint gene required for cell cycle arrest and DNA damage repair in response to DNA damage. This protein shares strong similarity with DNA replication factor C (RFC), and can form a complex with RFCs. This protein binds to chromatin prior to DNA damage and is phosphorylated by the checkpoint kinase ATR following damage. This protein recruits the RAD1-RAD9-HUS1 checkpoint protein complex onto chromatin after DNA damage, which may be required for its phosphorylation. The phosphorylation of this protein is required for the DNA-damage-induced cell cycle G2 arrest, and is thought to be a critical early event during checkpoint signaling in DNA-damaged cells. Multiple alternatively spliced transcript variants of this gene, which encode four distinct protein isoforms, have been reported. Two pseudogenes, located on chromosomes 7 and 13, have been identified. [provided by RefSeq, Jul 2013]
- ReactivityHuman
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC41116161





![Untreated (–) and treated (+) HeLa whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membranes were blotted with Rad17 (phospho Ser645) antibody [HL3676] (GTX641704) diluted at 1:500 and competitor's antibody () diluted at 1:. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.](https://www.genetex.com/upload/website/prouct_img/normal/GTX641704/GTX641704_T-45649_20250207_WB_treatment_UVC_25021320_850.webp)

