Mouse IgM (Fc specific) Rabbit Polyclonal Antibody

SKU
AP32992BT-N
Mouse IgM (Fc specific) rabbit polyclonal antibody, Biotin
  $820.00
2 Weeks*
Bulk/Customize
Specifications
Specifications
Product Data
Application ELISA, ID, IF, IHC, IP, WB
Recommended Dilution In immunocytochemical and immunohistochemical staining of IgM at the cellular and subcellular level of appropriately treated cell and tissue substrates; to demonstrate circulating IgM antibodies in serodiagnostic microbiology and autoimmune diseases; to identify a specific antigen using a reference antibody of mouse origin known to be of the IgM isotype in the middle layer of the indirect test procedure; in non-isotopic assay methodology (e.g. ELISA) to measure IgM in mouse serum or other body fluids. As a second step an avidin or streptavidin conjugate of the user’s choice has to be used. This immunoconjugate is not pre-diluted. The optimum working dilution of each conjugate should be established by titration before being used. Excess labelled antibody must be avoided because it may cause high unspecific background staining and interfere with the specific signal.
Recommended Working Dilutions:
Histochemical and cytochemical Use: 1/100- 1/2500.
ELISA and comparable non-precipitating antibody-binding assays: 1/1000- 1/5000.
Reactivity Mouse
Antibody Host Rabbit
Isotype IgG
Clonality Polyclonal
Immunogen Purified homogenous IgM isolated from Mouse serum. Immunization with intact and split IgM.
Freund’s complete adjuvant is used in the first step of the immunization procedure.
Specificity The reactivity of the antiserum is directed to the Fc subunit of the IgM molecule which expresses strict isotypic (class) specificity. It does not react with IgG, IgA and IgG/Fab or any non-Ig protein in mouse serum, as tested by immunoelectrophoresis and double radial immunodiffusion.
Cross-reactivity: Inter-species cross-reactivity is a normal feature of antibodies to immunoglobulins, since Ig of different species frequently share antigenic determinants. Cross-reactivity of this immunoconjugate has not been tested in detail.
Buffer PBS, pH 7.2
Label: Biotin
State: Lyophilized hyperimmune Ig fraction
Stabilizer: None
Preservative: None, as it may interfere with the antibody activity.
Molar radio: Biotin/IgG protein (B/P) ~ 4.7
Reconstitution Method Restore with 1 ml sterile distilled water.
Concentration 10.0 mg/ml
Purification Hyperimmune antisera with strong precipitating activity are selected for fractionation by salt precipitation and purification of the IgG fraction by DEAE Chromatography
Conjugation Biotin
Storage Store lyophilized at 2-8°C for 6 months or at -20°C long term.
After reconstitution store the antibody undiluted at 2-8°C for one month
or (in aliquots) at -20°C long term.
Avoid repeated freezing and thawing.
Shipping Ambient
Note Adsorption: Immunoaffinity adsorbed using insolubilized antigens as required to eliminate antibodies cross-reacting with other components of the immunoglobulin system or reacting with other serum proteins. Special attention is given to the removal of antibodies to common Ig/Fab. The use of insolubilized adsorption antigens prevents the presence of excess adsorbent protein or immune complexes in the antiserum.
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Documents
Resources

file-alt Citations

Telomerase reverse transcriptase interference synergistically promotes tumor necrosis factor‑related apoptosis‑inducing ligand‑induced oral squamous cell carcinoma apoptosis and suppresses proliferation in vitro and in vivo
Zhao, Zhang, Le et al
Int. J. Mol. Med. (2018)
AI Summary: OriGene's anti-hTERT antibodies (catalog numbers SP‑9001/9002) were used in this study to detect hTERT protein expression, enabling the researchers to assess the effects of hTERT silencing on oral squamous cell carcinoma apoptosis and proliferation.
Snippet: no. SP‑9001/9002;1:500;OriGene Technologies, Inc., Rockville, MD, USA) for 30 min at 37˚C. HRP‑conjugated streptavidin (Dako;Agilent Technologies, Inc., Santa Clara, CA, USA) was added to the slides before visualization of the antigen‑antibody complex with 3
Showing 1-1 of 1 papers.
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