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Goat anti-Mouse IgM (Heavy Chain) Antibody - Preadsorbed

ELISA, IHC, WB Polyclonal IgG unconjugated F(ab')2 fragment
Catalog No. ABIN965158
  • Target See all IgM products
    IgM
    Fragment
    F(ab')2 fragment
    Binding Specificity
    • 132
    • 109
    • 86
    • 41
    • 16
    • 8
    • 7
    • 1
    • 1
    Heavy Chain
    Reactivity
    • 185
    • 128
    • 65
    • 37
    • 30
    • 23
    • 22
    • 19
    • 14
    • 13
    • 13
    • 13
    • 13
    • 12
    • 11
    • 4
    • 2
    Mouse
    Host
    • 311
    • 176
    • 73
    • 15
    • 13
    • 5
    • 4
    • 1
    Goat
    Clonality
    • 483
    • 78
    Polyclonal
    Application
    • 311
    • 236
    • 227
    • 186
    • 143
    • 128
    • 64
    • 62
    • 47
    • 47
    • 46
    • 42
    • 38
    • 28
    • 20
    • 18
    • 13
    • 6
    • 5
    • 5
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC), Western Blotting (WB)
    Specificity
    F(ab')2 anti-Mouse IgM antibodyAssay by immunoelectrophoresis resulted in a single precipitin arc against anti-Goat Serum, Mouse IgM and Mouse Serum.
    Characteristics
    F(ab')2 anti-Mouse IgM antibody was generated by enzymatic cleavage and subsequent separation from the Fc fragment. Because of their smaller size, F(ab)2 fragments offer several advantages over intact antibodies for use in certain immunochemical techniques and experimental applications. F(ab)2 fragments penetrate into tissue samples and show better antigen recognition and signal generation in IHC. F(ab)2 fragments lack the Fc region and therefore do not bind Fc receptors which effectively lowers background staining. F(ab')2 Mouse IgM antibody is ideal for investigators who routinely perform flow cytometry, immunohistochemistry or IHC and other immunoassays.
    The antibody was prepared from monospecific antiserum by immunoaffinity chromatography using Mouse IgM coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities, pepsin digestion and chromatographic separation.
    Purification
    Preadsorption: Solid phase absorption
    Sterility
    Sterile filtered
    Immunogen

    Immunogen: Anti-Mouse IgM was produced by repeated immunization with Mouse IgM heavy chain in goat.

    Immunogen Type: Native Protein

    Isotype
    IgG
  • Application Notes

    Immunohistochemistry Dilution: 1:1,000 - 1:5,000

    Application Note: Suitable for immunomicroscopy and flow cytometry or FACS analysis as well as other antibody based assays requiring extremely low background levels, absence of F(c) mediated binding, lot-to-lot consistency, high titer and specificity. The maximum amount of reagent required to stain 1 x 10E6 cells in flow cytometry is approximately 1.0 μg of antibody. Lesser amounts of reagent may be sufficient for staining. Optimal titers for other applications should be determined by the researcher. As a general guideline dilutions of 1:100 to 1:250 should be suitable for most applications.

    ELISA Dilution: 1:2,000 - 1:8,000

    Western Blot Dilution: 1:200 - 1:2,000

    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.1 mg/mL
    Buffer

    Buffer: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2

    Stabilizer: None

    Preservative: 0.01 % (w/v) 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
    4 °C,-20 °C
    Storage Comment
    Store vial at 4 °C prior to restoration. For extended storage aliquot contents and freeze at -24 °C or below. This product is stable for several weeks at 4 °C as an undiluted liquid.
    Expiry Date
    12 months
  • Target
    IgM
    Abstract
    IgM Products
    Target Type
    Antibody
    Background

    Synonyms: Mouse F(ab')2 Antibody, Gt-a-Mouse IgM, Mouse F(ab')2 Antibody in goat, Mouse F(ab')2 Secondary Antibody.

    Background: F(ab')2 anti-Mouse IgM antibody was generated by enzymatic cleavage and subsequent separation from the Fc fragment. Because of their smaller size, F(ab)2 fragments offer several advantages over intact antibodies for use in certain immunochemical techniques and experimental applications. F(ab)2 fragments penetrate into tissue samples and show better antigen recognition and signal generation in IHC. F(ab)2 fragments lack the Fc region and therefore do not bind Fc receptors which effectively lowers background staining. F(ab')2 Mouse IgM antibody is ideal for investigators who routinely perform flow cytometry, immunohistochemistry or IHC and other immunoassays.

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