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Complement Factor H antibody (AA 527-588)

This anti-Complement Factor H antibody is a Rabbit Polyclonal antibody detecting Complement Factor H in WB. Suitable for Human.
Catalog No. ABIN1886532

Quick Overview for Complement Factor H antibody (AA 527-588) (ABIN1886532)

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

    • 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

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    527 - 588 of Human Complement factor H
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

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

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Storage

    4 °C/-20 °C

    Storage Comment

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

    Complement Factor H (CFH)

    Alternative Name

    Complement factor H

    Background

    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]

    Molecular Weight

    139 kDa

    Gene ID

    3075

    NCBI Accession

    NP_000177, NM_000186

    Pathways

    Complement System, Cellular Response to Molecule of Bacterial Origin
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