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KRCC1 Antikörper (AbBy Fluor® 350)

Dieses Anti-KRCC1-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von KRCC1 in WB und IF (p). Geeignet für Human, Maus und Ratte.
Produktnummer ABIN1403421

Kurzübersicht für KRCC1 Antikörper (AbBy Fluor® 350) (ABIN1403421)

Target

KRCC1 (Lysine-Rich Coiled-Coil 1 (KRCC1))

Reaktivität

  • 26
  • 17
  • 16
  • 2
  • 1
Human, Maus, Ratte

Wirt

  • 26
Kaninchen

Klonalität

  • 26
Polyklonal

Konjugat

  • 8
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser KRCC1 Antikörper ist konjugiert mit AbBy Fluor® 350

Applikation

  • 21
  • 12
  • 6
  • 3
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Kreuzreaktivität

    Human, Maus, Ratte

    Aufreinigung

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human KRCC1

    Isotyp

    IgG
  • Applikationshinweise

    IF(IHC-P) 1:50-200

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Konservierungsmittel

    ProClin

    Vorsichtsmaßnahmen

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Haltbarkeit

    12 months
  • Target

    KRCC1 (Lysine-Rich Coiled-Coil 1 (KRCC1))

    Andere Bezeichnung

    KRCC1

    Hintergrund

    Synonyms: CHBP2, cryptogenic hepatitis binding protein, Cryptogenic hepatitis-binding protein 2, KRCC1, KRCC1_HUMAN, lysine rich coiled coil 1, Lysine-rich coiled-coil protein 1.

    Background: KRCC1 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, Alstr 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.

    Gen-ID

    51315
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