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CFP antibody (AA 197-223)

The Rabbit Polyclonal anti-CFP antibody has been validated for WB, ELISA and FACS. It is suitable to detect CFP in samples from Human.
Catalog No. ABIN3030563

Quick Overview for CFP antibody (AA 197-223) (ABIN3030563)

Target

See all CFP Antibodies
CFP (Complement Factor P (CFP))

Reactivity

  • 54
  • 33
  • 10
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 52
  • 7
  • 3
Rabbit

Clonality

  • 56
  • 6
Polyclonal

Conjugate

  • 26
  • 10
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CFP antibody is un-conjugated

Application

  • 42
  • 21
  • 13
  • 11
  • 10
  • 7
  • 7
  • 7
  • 5
  • 5
  • 5
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 15
    • 6
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 197-223

    Purification

    Antigen affinity purified

    Immunogen

    A portion of amino acids 197-223 from the human protein was used as the immunogen for this CFP antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Titration of the CFP antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000,Flow Cytometry: 1:10-1:50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    In 1X PBS, pH 7.4, with 0.09 % sodium azide

    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

    Aliquot the CFP antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    CFP (Complement Factor P (CFP))

    Alternative Name

    CFP

    Background

    This gene encodes a plasma glycoprotein that positively regulates the alternative complement pathway of the innate immune system. This protein binds to many microbial surfaces and apoptotic cells and stabilizes the C3- and C5-convertase enzyme complexes in a feedback loop that ultimately leads to formation of the membrane attack complex and lysis of the target cell. Mutations in this gene result in two forms of properdin deficiency, which results in high susceptibility to meningococcal infections.

    UniProt

    P27918

    Pathways

    Complement System
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