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Complement C2 antibody

The Rabbit Polyclonal anti-Complement C2 antibody has been validated for WB, ICC and IF. It is suitable to detect Complement C2 in samples from Human.
Catalog No. ABIN2856098

Quick Overview for Complement C2 antibody (ABIN2856098)

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), Immunocytochemistry (ICC), Immunofluorescence (IF)
  • Cross-Reactivity

    Human

    Characteristics

    Rabbit Polyclonal antibody to Complement C2 (complement component 2)
    Complement C2 antibody [N3C3]

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human Complement C2. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: 293T , A431 , H1299 , HeLaS3 , HepG2 , Molt-4 , Raji

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 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.

    Cellular Localization: Secreted

    Molecular Weight

    83 kDa

    Gene ID

    717

    UniProt

    P06681
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