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Complement Factor H antibody

The Rabbit Monoclonal anti-Complement Factor H antibody has been validated for WB. It is suitable to detect Complement Factor H in samples from Human.
Catalog No. ABIN7266479
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$310.25
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Quick Overview for Complement Factor H antibody (ABIN7266479)

Target

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

Reactivity

  • 80
  • 13
  • 12
  • 2
  • 2
Human

Host

  • 65
  • 27
  • 3
  • 2
  • 1
Rabbit

Clonality

  • 52
  • 45
  • 1
Monoclonal

Conjugate

  • 57
  • 10
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
This Complement Factor H antibody is un-conjugated

Application

  • 71
  • 33
  • 26
  • 26
  • 22
  • 15
  • 13
  • 6
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Purpose

    Complement factor H Rabbit mAb

    Cross-Reactivity

    Human

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human Complement factor H

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Complement Factor H (CFH)

    Alternative Name

    CFH

    Background

    This gene is a member of the Regulator of Complement Activation (RCA) gene cluster and encodes a protein with twenty short consensus 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, Oct 2011],AHUS1, AMBP1, ARMD4, ARMS1, CFHL3, FH, FHL1, HF, HF1, HF2, HUS,Cell Intrinsic Innate Immunity Signaling Pathway,Immunology & Inflammation,CFH

    Molecular Weight

    180kDa

    Gene ID

    3075

    UniProt

    P08603

    Pathways

    Complement System, Cellular Response to Molecule of Bacterial Origin
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