Rat Breast cancer type 1 susceptibility protein ELISA Kit | Brca1 elisa kit

Rat Breast cancer type 1 susceptibility protein homolog ELISA Kit

Cat. Num. AAA2886984

• Reactivity: Rat
• Synonyms: Breast cancer type 1 susceptibility protein; Rat Breast cancer type 1 susceptibility protein homolog ELISA Kit; Breast cancer type 1 susceptibility protein homolog; Brca1; Brca1 elisa kit

• Reactivity: Rat
• Sequence Length: 1817

• Preparation and Storage: For long term storage, please store the entire kit at -20 degree C.

Typical Testing Data/Standard Curve (for reference only)

NCBI and Uniprot Product Information

• NCBI GI #: 6978573
• NCBI GeneID: 497672
• NCBI Accession #: NP_036646.1
• NCBI GenBank Nucleotide #: NM_012514.1
• UniProt Accession #: O54952; P97951
• Molecular Weight: 199,879 Da
• NCBI Official Full Name: breast cancer type 1 susceptibility protein homolog
• NCBI Official Synonym Full Names: breast cancer 1, early onset
• NCBI Official Symbol: Brca1
• NCBI Protein Information: breast cancer type 1 susceptibility protein homolog
• UniProt Protein Name: Breast cancer type 1 susceptibility protein homolog
• Protein Family: Breast cancer type 1 susceptibility protein
• UniProt Gene Name: Brca1
• UniProt Entry Name: BRCA1_RAT

NCBI Description

involved in the DNA damage response and DNA repair [RGD, Feb 2006]

Uniprot Description

BRCA1: the BRCA1-BARD1 heterodimer coordinates a diverse range of cellular pathways such as DNA damage repair, ubiquitination and transcriptional regulation to maintain genomic stability. Acts by mediating ubiquitin E3 ligase activity that is required for its tumor suppressor function. Plays a central role in DNA repair by facilitating cellular response to DNA repair. Required for appropriate cell cycle arrests after ionizing irradiation in both the S-phase and the G2 phase of the cell cycle. Involved in transcriptional regulation of P21 in response to DNA damage. Required for FANCD2 targeting to sites of DNA damage. May function as a transcriptional regulator. Inhibits lipid synthesis by binding to inactive phosphorylated ACC1 and preventing its dephosphorylation. Defects in BRCA1 are a cause of genetic susceptibility to breast cancer. Mutations in BRCA1 are thought to be responsible for more than 80% of inherited breast-ovarian cancer. Part of the BRCA1-associated genome surveillance complex (BASC), which contains BRCA1, MSH2, MSH6, MLH1, ATM, BLM, PMS2 and the RAD50-MRE11-NBN protein complex. This association may be a dynamic process changing throughout the cell cycle and within subnuclear domains. Interacts (via BRCT domains) with CTIP. Associates with RNA polymerase II holoenzyme. Interacts with SMC1 and COBRA1. Interacts (via BRCT domains) with BRIP1. Interacts with FANCD2 (ubiquitinated). Interacts with BAP1. Interacts with Artemis and claspin. Interacts with H2AFX (phosphorylated on S140). Interacts with CHK1. Interacts with BRCC3. Five human isoforms are produced by alternative splicing and alternative initiation. Isoform 1 and isoform 3 are widely expressed. Isoform 1 is largely nuclear, while isoforms 3 and 5 are cytoplasmic.

Protein type: EC 6.3.2.-; Ubiquitin ligase; Transcription, coactivator/corepressor; Tumor suppressor; Nuclear receptor co-regulator; Ubiquitin conjugating system

Cellular Component: BRCA1-BARD1 complex; chromosome; condensed chromosome; condensed nuclear chromosome; cytoplasm; mitochondrial matrix; nucleus; plasma membrane; protein complex; ribonucleoprotein complex

Molecular Function: chromatin binding; damaged DNA binding; DNA binding; enzyme binding; ligase activity; protein binding; RNA binding; ubiquitin protein ligase binding; ubiquitin-protein ligase activity; zinc ion binding

Biological Process: brain development; centrosome cycle; chordate embryonic development; chromosome breakage; chromosome segregation; DNA damage response, signal transduction resulting in induction of apoptosis; DNA recombination; DNA replication; dosage compensation, by inactivation of X chromosome; double-strand break repair; double-strand break repair via homologous recombination; fatty acid biosynthetic process; genetic imprinting; negative regulation of estrogen receptor signaling pathway; negative regulation of fatty acid biosynthetic process; negative regulation of histone acetylation; negative regulation of histone H3-K4 methylation; negative regulation of histone H3-K9 methylation; negative regulation of transcription, DNA-dependent; positive regulation of angiogenesis; positive regulation of DNA repair; positive regulation of histone acetylation; positive regulation of histone H3-K4 methylation; positive regulation of histone H3-K9 methylation; positive regulation of protein import into nucleus, translocation; positive regulation of protein ubiquitination; positive regulation of transcription from RNA polymerase II promoter; positive regulation of transcription, DNA-dependent; postreplication repair; protein autoubiquitination; protein ubiquitination; regulation of cell proliferation; response to DNA damage stimulus; response to estradiol stimulus; response to estrogen stimulus; response to ionizing radiation; response to lipid; response to nutrient; response to organic substance; transcription, DNA-dependent