PIPA595666

Phospho-CtIP (Thr847) Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA595666-Each-of-1 In Stock ₹ 49,439.50

PIPA595666 - Each of 1

₹ 49,439.50

In Stock

Quantity

1

Base Price: ₹ 49,439.50

GST (18%): ₹ 8,899.11

Total Price: ₹ 58,338.61

Antigen

Phospho-CtIP (Thr847)

Classification

Polyclonal

Conjugate

Unconjugated

Gene

Rbbp8

Gene Alias

9930104E21Rik, COM1, CtBP-interacting protein, CtIP, DNA endonuclease RBBP8, JWDS, RB binding protein 8, endonuclease, RBBP8, RBBP-8, retinoblastoma binding protein 8, retinoblastoma-binding protein 8, Retinoblastoma-interacting protein and myosin-like, RGD1308872, RIM, SAE2, SCKL2, Sporulation in the absence of SPO11 protein 2 homolog

Host Species

Rabbit

Purification Method

Antigen Affinity Chromatography

Regulatory Status

RUO

Gene ID (Entrez)

5932

Content And Storage

-20°, C, Avoid Freeze/Thaw Cycles

Form

Liquid

Applications

Western Blot

Concentration

∽0.15 mg/mL

Formulation

10mM HEPES with 0.15M NaCl, 100μg/mL BSA, 50% glycerol and no preservative, pH 7.5

Gene Accession No.

Q99708

Gene Symbols

Rbbp8

Immunogen

Synthetic phospho-peptide corresponding to amino acid residues surrounding Thr847 conjugated to KLH

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

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Description

  • Antigen Affinity Purified from Pooled Serum CtIP, a 125 kD protein, was originally found interacting with a transcription repressor, CtBP, through the PLDLS motif (CtBP-Interacting Protein) thus suggested a role in transcription
  • Studies have shown that CtIP also interacts with BRCA1 protein through the c-terminus BRCT domains also suggested that CtIP is a potential tumor suppressor
  • This CtIP-BRCA1 interaction can be disrupted by DNA damaging agents including UV or gamma-irradiation
  • Li et al (Nature 406, 210 - 215 (2000)) have shown that ATM phosphorylates CtIP at serine residues 664 and 745, and mutation of these sites abrogates the dissociation of BRCA1 from CtIP, resulting in persistent repression of BRCA1-dependent induction of GADD45 upon ionizing radiation.