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KRCC1 anticorps

KRCC1 Reactivité: Humain, Souris WB, ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7247672
  • Antigène Tous les produits KRCC1
    KRCC1 (Lysine-Rich Coiled-Coil 1 (KRCC1))
    Reactivité
    • 26
    • 17
    • 17
    • 2
    • 1
    Humain, Souris
    Hôte
    • 26
    Lapin
    Clonalité
    • 26
    Polyclonal
    Conjugué
    • 7
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp KRCC1 est non-conjugé
    Application
    • 21
    • 13
    • 5
    • 3
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Fusion protein of human KRCC1
    Isotype
    IgG
  • Indications d'application
    WB 1:500-1:2000, IHC 1:100-1:300, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.68 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    KRCC1 (Lysine-Rich Coiled-Coil 1 (KRCC1))
    Autre désignation
    KRCC1 (KRCC1 Produits)
    Synonymes
    anticorps DKFZp468N1119, anticorps CHBP2, anticorps AA792894, anticorps RGD1306495, anticorps lysine rich coiled-coil 1, anticorps lysine-rich coiled-coil 1, anticorps KRCC1, anticorps Krcc1
    Sujet
    KRCC1 (lysine-rich coiled-coil 1), also known as CHBP2 (cryptogenic hepatitis-binding protein 2), is a 259 amino acid protein that is encoded by a gene located on human chromosome 2p11.2. Consisting of 237 million bases, chromosome 2 is the second largest human chromosome and encodes over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstrm syndrome, is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.
    Poids moléculaire

    Observed_MW: Refer to figures

    Calculated_MW: 31 kDa

    UniProt
    Q9NPI7
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