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Complement C2 antibody (AA 265-612)

The Rabbit Polyclonal anti-Complement C2 antibody has been validated for WB and IF. It is suitable to detect Complement C2 in samples from Human.
Catalog No. ABIN1886288

Quick Overview for Complement C2 antibody (AA 265-612) (ABIN1886288)

Target

See all Complement C2 Antibodies
Complement C2

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This Complement C2 antibody is un-conjugated

Application

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Western Blotting (WB), Immunofluorescence (IF)
  • Binding Specificity

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    AA 265-612

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 265 and 612 of Human C2
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunofluorescence: 1.100-1.200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % 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 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.

    Molecular Weight

    83 kDa

    Gene ID

    717

    NCBI Accession

    NP_000054, NM_000063
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