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Complement C2 antibody (N-Term)

This anti-Complement C2 antibody is a Rabbit Polyclonal antibody detecting Complement C2 in WB. Suitable for Human and Hamster.
Catalog No. ABIN951633

Quick Overview for Complement C2 antibody (N-Term) (ABIN951633)

Target

See all Complement C2 Antibodies
Complement C2

Reactivity

  • 60
  • 12
  • 11
  • 8
  • 5
  • 4
  • 4
  • 3
  • 2
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  • 1
  • 1
Human, Hamster

Host

  • 53
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Rabbit

Clonality

  • 56
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Polyclonal

Conjugate

  • 37
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Complement C2 antibody is un-conjugated

Application

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  • 5
  • 4
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  • 1
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Western Blotting (WB)
  • Binding Specificity

    • 15
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    • 6
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    • 1
    • 1
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    AA 150-180, N-Term

    Specificity

    This antibody reacts to Complement C2.

    Cross-Reactivity (Details)

    Species reactivity (tested):Human and Hamster.

    Purification

    Affinity chromatography on Protein A

    Immunogen

    KLH conjugated synthetic peptide between 150-180 amino acids from the N-terminal region of human C2
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS containing 0.09 % (W/V) sodium azide as preservative

    Preservative

    Sodium azide

    Precaution of Use

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

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    Complement C2

    Background

    Component C2 is a serum glycoprotein that functions as part of the classical pathway of the complement system. Activated C1 cleaves C2 into C2a and C2b. The serine proteinase C2a then combines with complement factor 4b to create the C3 or C5 convertase. Deficiency of C2 has been reported to associated with certain autoimmune diseases and SNPs in this gene have been associated with altered susceptibility to age-related macular degeneration. This gene localizes within the class III region of the MHC on the short arm of chromosome 6. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described in publications but their full-length sequence has not been determined.Synonyms: C2, C3/C5 convertase, Complement component 2

    Gene ID

    717

    NCBI Accession

    NP_000054
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