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Retinoblastoma 1 (RB1) (N-Term) Peptide

RB1 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN982701
  • Antigène Tous les produits Retinoblastoma 1 (RB1)
    Retinoblastoma 1 (RB1)
    Protein Region
    N-Term
    Origine
    Humain
    Source
    • 11
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Séquence
    MPPKTPRKTA ATAAAAAAEP PAPPPPPPPE EDPEQDSGPE DLPLVRLEFE
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti-RB1 Antibody(ARP58065_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    Purification
    Purified
  • Indications d'application
    Each Investigator should determine their own optimal working dilution for specific applications.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Concentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Conseil sur la manipulation
    Avoid repeated freeze-thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène
    Retinoblastoma 1 (RB1)
    Synonymes
    OSRC Peptide, RB Peptide, p105-Rb Peptide, pRb Peptide, pp110 Peptide, Rb Peptide, Rb-1 Peptide, P105-RB Peptide, PP110 Peptide, RB11 Peptide, zgc:154147 Peptide, RB transcriptional corepressor 1 Peptide, RB transcriptional corepressor like 1 Peptide, retinoblastoma 1 Peptide, RB1 Peptide, RBL1 Peptide, Rb1 Peptide, rb1 Peptide
    Sujet
    The protein encoded by this gene is a negative regulator of the cell cycle and was the first tumor suppressor gene found. The encoded protein also stabilizes constitutive heterochromatin to maintain the overall chromatin structure. The active, hypophosphorylated form of the protein binds transcription factor E2F1. Defects in this gene are a cause of childhood cancer retinoblastoma (RB), bladder cancer, and osteogenic sarcoma.

    Alias Symbols: OSRC, RB, pRb, pp110, p105-Rb

    Protein Interaction Partner: AATF,ABL1,AR,ATF2,BDP1,BGLAP,BIRC5,BNC2,BRCA1,BRD2,BRD8,CASP10,CASP2,CASP3,CASP6,CASP7,CASP8,CASP9,CCND1,CDK2,CDK4,CDK6,CDK6,CDKN1A,CEBPD,CEBPE,DNMT1,E1A,E2F1,E2F1,E2F1,E2F1,E2F1,E2F1,E2F2,E2F2,E2F2,EID1,EID1,EPO,FRK,GNB2L1,GTF3C2,HDAC1,HDAC1,HIF1A,HMGB1,

    Protein Size: 928
    Poids moléculaire
    106 kDa
    ID gène
    5925
    NCBI Accession
    NM_000321, NP_000312
    UniProt
    P06400
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