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DPCR1 Antikörper (PE-Cy5)

Dieses Anti-DPCR1-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von DPCR1 in WB. Geeignet für Human.
Produktnummer ABIN1434234

Kurzübersicht für DPCR1 Antikörper (PE-Cy5) (ABIN1434234)

Target

Alle DPCR1 Antikörper anzeigen
DPCR1 (Diffuse Panbronchiolitis Critical Region 1 (DPCR1))

Reaktivität

Human

Wirt

  • 29
Kaninchen

Klonalität

  • 29
Polyklonal

Konjugat

  • 7
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser DPCR1 Antikörper ist konjugiert mit PE-Cy5

Applikation

  • 28
  • 13
  • 8
  • 3
Western Blotting (WB)
  • Kreuzreaktivität

    Human

    Aufreinigung

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human DPCR1

    Isotyp

    IgG
  • 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

    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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Haltbarkeit

    12 months
  • Target

    DPCR1 (Diffuse Panbronchiolitis Critical Region 1 (DPCR1))

    Andere Bezeichnung

    DPCR1

    Hintergrund

    Synonyms: Dfuse panbronchiolitis critical region 1, Dfuse panbronchiolitis critical region, Dfuse panbronchiolitis critical region protein 1, DKFZp666O235, DPCR protein, MGC126710, MGC126712, OTTHUMP00000062447, PBLT, bCX105N19.6, DPCR1_HUMAN.

    Background: Making up nearly 6 % of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer, suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6.

    Molekulargewicht

    56kDa

    Gen-ID

    135656
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