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KRCC1 Antikörper

KRCC1 Reaktivität: Human, Maus WB, ELISA, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7247672
  • Target Alle KRCC1 Produkte
    KRCC1 (Lysine-Rich Coiled-Coil 1 (KRCC1))
    Reaktivität
    • 26
    • 17
    • 17
    • 2
    • 1
    Human, Maus
    Wirt
    • 26
    Kaninchen
    Klonalität
    • 26
    Polyklonal
    Konjugat
    • 7
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser KRCC1 Antikörper ist unkonjugiert
    Applikation
    • 21
    • 13
    • 5
    • 3
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Antigen affinity purification
    Immunogen
    Fusion protein of human KRCC1
    Isotyp
    IgG
  • Applikationshinweise
    WB 1:500-1:2000, IHC 1:100-1:300, ELISA 1:5000-1:10000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1.68 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    KRCC1 (Lysine-Rich Coiled-Coil 1 (KRCC1))
    Andere Bezeichnung
    KRCC1 (KRCC1 Produkte)
    Synonyme
    DKFZp468N1119 antikoerper, CHBP2 antikoerper, AA792894 antikoerper, RGD1306495 antikoerper, lysine rich coiled-coil 1 antikoerper, lysine-rich coiled-coil 1 antikoerper, KRCC1 antikoerper, Krcc1 antikoerper
    Hintergrund
    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.
    Molekulargewicht

    Observed_MW: Refer to figures

    Calculated_MW: 31 kDa

    UniProt
    Q9NPI7
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