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Complement Factor H Antikörper (AA 527-588)

Dieses Anti-Complement Factor H-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von Complement Factor H in WB. Geeignet für Human.
Produktnummer ABIN1886532

Kurzübersicht für Complement Factor H Antikörper (AA 527-588) (ABIN1886532)

Target

Alle Complement Factor H (CFH) Antikörper anzeigen
Complement Factor H (CFH)

Reaktivität

  • 78
  • 15
  • 14
  • 3
  • 2
Human

Wirt

  • 63
  • 33
  • 3
  • 2
Kaninchen

Klonalität

  • 59
  • 41
  • 1
Polyklonal

Konjugat

  • 64
  • 12
  • 7
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Dieser Complement Factor H Antikörper ist unkonjugiert

Applikation

  • 78
  • 49
  • 32
  • 32
  • 26
  • 17
  • 14
  • 6
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Bindungsspezifität

    • 9
    • 9
    • 6
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 527-588

    Aufreinigung

    Purified by antigen-affinity chromatography.

    Immunogen

    527 - 588 of Human Complement factor H
  • Applikationshinweise

    Suggested dilutions:
    Western blotting: 1.500-1.3000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    1 x PBS, 1 % BSA, 20 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Konservierungsmittel

    Thimerosal (Merthiolate)

    Vorsichtsmaßnahmen

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

    Complement Factor H (CFH)

    Andere Bezeichnung

    Complement factor H

    Hintergrund

    This gene is a member of the Regulator of Complement Activation (RCA) gene cluster and encodes a protein with twenty short concensus repeat (SCR) domains.This protein is secreted into the bloodstream and has an essential role in the regulation of complement activation, restricting this innate defense mechanism to microbial infections.Mutations in this gene have been associated with hemolytic-uremic syndrome (HUS) and chronic hypocomplementemic nephropathy.Alternate transcriptional splice variants, encoding different isoforms, have been characterized.[provided by RefSeq]

    Molekulargewicht

    139 kDa

    Gen-ID

    3075

    NCBI Accession

    NP_000177, NM_000186

    Pathways

    Komplementsystem, Cellular Response to Molecule of Bacterial Origin
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