BRCA1 anticorps (AA 341-748)
Aperçu rapide pour BRCA1 anticorps (AA 341-748) (ABIN7468063)
Antigène
Voir toutes BRCA1 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
Classe de qualité
Clone
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Épitope
- AA 341-748
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Specificité
- This antibody recognizes BRCA1, a 220- kDa nuclear phosphoprotein, and does not recognize the exon 11 splice variant. Mutations in this tumor suppressor gene greatly increase the risk of breast cancer.
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Réactivité croisée
- Humain
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Purification
- Protein G purified
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Immunogène
- BRCA1 protein fragment expressed in E. coli corresponding to amino acids 341-748.
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Isotype
- IgG1
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Indications d'application
- WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
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Commentaires
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Positive Control: 293T , MCF7 , U2OS , HeLa Validation: KO/KD
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 2.75 mg/mL
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Buffer
- PBS, No Preservative
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Agent conservateur
- Without preservative
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- BRCA1 (Breast Cancer 1 (BRCA1))
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Autre désignation
- BRCA1 DNA repair associated
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Sujet
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Synonyms: BRCA1 DNA repair associated , BRCAI , BRCC1 , BROVCA1 , FANCS , IRIS , PNCA4 , PPP1R53 , PSCP , RNF53
Background: This gene encodes a nuclear phosphoprotein that plays a role in maintaining genomic stability, and it also acts as a tumor suppressor. The encoded protein combines with other tumor suppressors, DNA damage sensors, and signal transducers to form a large multi-subunit protein complex known as the BRCA1-associated genome surveillance complex (BASC). This gene product associates with RNA polymerase II, and through the C-terminal domain, also interacts with histone deacetylase complexes. This protein thus plays a role in transcription, DNA repair of double-stranded breaks, and recombination. Mutations in this gene are responsible for approximately 40 % of inherited breast cancers and more than 80 % of inherited breast and ovarian cancers. Alternative splicing plays a role in modulating the subcellular localization and physiological function of this gene. Many alternatively spliced transcript variants, some of which are disease-associated mutations, have been described for this gene, but the full-length natures of only some of these variants has been described. A related pseudogene, which is also located on chromosome 17, has been identified. [provided by RefSeq, May 2009]
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Poids moléculaire
- 208 kDa
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ID gène
- 672
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UniProt
- P38398
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Pathways
- Cycle Cellulaire, Réparation de l'ADN, Intracellular Steroid Hormone Receptor Signaling Pathway, Positive Regulation of Response to DNA Damage Stimulus
Antigène
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