BRCA1 Interacting Protein C-Terminal Helicase 1 Peptide 3


Background

Catalog Number:

CPTC-BRIP1-5

Target Antigen:

BRCA1 Interacting Protein C-Terminal Helicase 1 Peptide 3

Isotype:

IgG

Species:

Rabbit Monoclonal Antibody

Last Updated:

10/10/2019

Antigen Recognition(s):

Peptide, Phosphorylation

SOP:

External Links
Characterization Data [Compare Characterization Data]
  Immuno-MRM
Click to enlarge image Immuno-MRM chromatogram of CPTC-BRIP1-5 antibody (see CPTAC assay portal for details:
https://assays.cancer.gov/CPTAC-3281) Click image to enlarge

CPTC-BRIP1-5 iMRM

Result: Positive

Immuno-MRM chromatogram of CPTC-BRIP1-5 antibody (see CPTAC assay portal for details:
https://assays.cancer.gov/CPTAC-3281)


Background

NCI Identification Number:

00231

Antigen Name:

BRCA1 Interacting Protein C-Terminal Helicase 1 Peptide 3

CPTC Name:

CPTC-BRIP1 Peptide 3

Keywords:

BRCA1 Interacting Protein C-Terminal Helicase 1; BACH1; FANCJ; BRCA1/BRCA2-Associated Helicase 1; ATP-Dependent RNA Helicase BRIP1; BRCA1-Associated C-Terminal Helicase 1; OF; BRCA1-Binding Helicase-Like Protein; Fanconi Anemia Group J Protein; EC 3.6.4.13; BRCA1-Interacting Protein 1; RCA1-Interacting Protein C-Terminal Helicase 1; Protein FACJ; EC 3.6.1

Function:

The protein encoded by this gene is a member of the RecQ DEAH helicase family and interacts with the BRCT repeats of breast cancer, type 1 (BRCA1). The bound complex is important in the normal double-strand break repair function of breast cancer, type 1 (BRCA1). This gene may be a target of germline cancer-inducing mutations.

BRIP1 (BRCA1 interacting protein C-terminal helicase 1) is a protein-coding gene. Diseases associated with BRIP1 include brip1-related fanconi anemia, and brip1-related breast cancer. GO annotations related to this gene include ATP-dependent DNA helicase activity and 4 iron, 4 sulfur cluster binding. An important paralog of this gene is DDX11.

DNA-dependent ATPase and 5' to 3' DNA helicase required for the maintenance of chromosomal stability. Acts late in the Fanconi anemia pathway, after FANCD2 ubiquitination. Involved in the repair of DNA double-strand breaks by homologous recombination in a manner that depends on its association with BRCA1.

Chromosomal Localization:

17q22.2

NCBI Accession Number:

NP_114432.2

Swiss Prot Accession Number:

Q9BX63

DNA Source:

N/A

Immunogen:

Synthetic Peptide

Vector Name:

N/A

Extinction Coefficient:

Buffers:

Expressed Sequence:

YSTPPYLLEAASHL(pS)PENFVEDEAK (pS930))

Native Sequence:

Calculated Isoelectric Point:

0

Molecular Weight:

2750

Last Updated:

03/08/2018

Links

Characterization Data

SOPs

No SOPs available.

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