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Render Timestamp: 2024-07-26T10:20:04.205Z
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PDP - Template Name: Secondary Antibody
PDP - Template ID: *******76815a7

Anti-Human IgA, alpha-Chain Specific, HRP-Linked Antibody #80403

    Supporting Data

    REACTIVITY H
    SENSITIVITY
    MW (kDa)
    Source/Isotype Goat
    Species Cross-Reactivity Key:
    • H-Human 

    Product Information

    Product Description

    Affinity purified goat Anti-Human IgA, alpha-Chain Specific antibody is conjugated to horseradish peroxidase (HRP). This product has been optimized for use as a secondary antibody in Western blotting and ELISA applications.

    Product Usage Information

    Reconstitute with 2.0 ml of dH20 to create a 0.8 mg/ml working solution. Centrifuge if the solution is not clear. It is recommended to prepare the working solution on day of use.

    Recommended Antibody Dilutions:

    ELISA (chromogenic substrates): 1:5K-1:100K

    Western Blotting (chromogenic substrates): 1:5K - 1:100K

    Western Blotting (ECL substrates): 1:10K - 1:200K

    Recommended antibody dilutions are provided in ranges because the optimal dilution is dependent on many factors, such as antigen density and permeability.

    Storage

    Supplied lyophilized with a formulation of 0.01M Sodium Phosphate (pH 7.6), 0.25M NaCl, and 15 mg/ml bovine serum albumin (BSA). Store lyophilized at 4ºC. In lyophilized form, the product is stable for 24 months. Once in solution, store at -80ºC or add glycerol (ACS grade or better) to a final concentration of 50% and store at -20ºC. Solutions should be used within 12 months. Aliquot to avoid multiple freeze/thaw cycles.

    Specificity / Sensitivity

    Anti-Human IgA, alpha-Chain Specific, HRP-Linked Antibody detects the heavy chain of human IgA but not human IgG or IgM. This antibody does not detect other non-immunoglobulin serum proteins. It may cross-react with IgA from other species.


    Species Reactivity:

    Human

    Source / Purification

    Anti-Human IgA, alpha-Chain Specific, HRP-Linked Antibody is produced by immunizing goats with human IgA. The Anti-Human IgA, alpha-Chain is purified from antisera by immunoaffinity chromatography using antigens coupled to agarose beads.

    Background

    Chemiluminescence systems have emerged as the best all-around method for western blot detection. They eliminate the hazards associated with radioactive materials and toxic chromogenic substrates. The speed and sensitivity of these methods are unequalled by traditional alternatives, and because results are generated on film, it is possible to record and store data permanently. Blots detected with chemiluminescent methods are easily stripped for subsequent reprobing with additional antibodies. HRP-conjugated secondary antibodies are utilized in conjunction with specific chemiluminescent substrates to generate the light signal. HRP conjugates have a very high turnover rate, yielding good sensitivity with short reaction times.

      For Research Use Only. Not For Use In Diagnostic Procedures.
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