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Complement Factor H antibody (Center)

This Rabbit Polyclonal antibody specifically detects Complement Factor H in WB, IHC and IF. It exhibits reactivity toward Human.
Catalog No. ABIN2797150

Quick Overview for Complement Factor H antibody (Center) (ABIN2797150)

Target

See all Complement Factor H (CFH) Antibodies
Complement Factor H (CFH)

Reactivity

  • 78
  • 15
  • 14
  • 3
  • 2
Human

Host

  • 63
  • 33
  • 3
  • 2
Rabbit

Clonality

  • 59
  • 41
  • 1
Polyclonal

Conjugate

  • 64
  • 12
  • 7
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
This Complement Factor H antibody is un-conjugated

Application

  • 78
  • 48
  • 32
  • 32
  • 26
  • 16
  • 14
  • 6
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Binding Specificity

    • 9
    • 8
    • 6
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 751-780, Center

    Purpose

    Rabbit Anti-Human CFH (Center) Antibody

    Immunogen

    This CFH antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 751-780 amino acids from the Central region of human CFH.

    Isotype

    Ig Fraction
  • Application Notes

    Western Blot, Immunohistochemistry, Immunofluorescence
    Recommended Dilutions
    WB: 1:1000, IHC: 1:50-100, IF: 1:10-50CFH Antibody (Center) .

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.287 mg/mL

    Storage

    4 °C,-20 °C

    Storage Comment

    2-8°C (short-term), -20°C (long-term)
  • Target

    Complement Factor H (CFH)

    Alternative Name

    CFH

    Background

    Target Description: 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.

    Gene Symbol: CFH

    Molecular Weight

    139096 Da

    Gene ID

    3075

    UniProt

    P08603

    Pathways

    Complement System, Cellular Response to Molecule of Bacterial Origin
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