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Purified NA/LE Rat Anti-Mouse IL-3
Product Details
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BD Pharmingen™
Mouse (QC Testing)
Rat IgG1
Recombinant mouse IL-3
ELISA (Routinely Tested), Flow cytometry, Neutralization (Tested During Development)
1.0 mg/ml
AB_395356
No azide/low endotoxin: Aqueous buffered solution containing no preservative, 0.2µm sterile filtered. Endotoxin level is ≤0.01 EU/µg (≤0.001 ng/µg) of protein as determined by the LAL assay.
RUO


Preparation And Storage

Store undiluted at 4°C. The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. This preparation contains no preservatives, thus it should be handled under aseptic conditions.

Recommended Assay Procedures

ELISA:  The purified MP2-8F8 antibody (Cat. No. 554381) is useful as a capture antibody for a sandwich ELISA for measuring mouse IL-3 protein levels.  Purified MP2-8F8 antibody can be paired with the biotinylated MP2-43D11 antibody (Cat. No. 554384) as the detecting antibody, with recombinant mouse IL-3 (Cat. No. 554579) as the standard.  For testing mouse IL-3 in complex biological fluids, such as serum or plasma, investigators may wish to consider using the BD OptEIA™ Mouse IL-3 ELISA Set (Cat. No. 555228).

Product Notices

  1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
  2. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
554379 Rev. 3
Antibody Details
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MP2-8F8

The MP2-8F8 antibody reacts with mouse interleukin-3 (IL-3). The immunogen used to generate the MP2-8F8 hybridoma was COS-expressed recombinant mouse IL-3.

554379 Rev. 3
Format Details
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NA/LE
NA/LE refers to the culture and purification methods and buffer used to produce purified antibodies with no azide and low endotoxin: Aqueous buffered solution containing no preservative, 0.2µm sterile filtered. Endotoxin level is ≤0.01 EU/µg (≤0.001 ng/µg) of protein as determined by the LAL assay.NA/LE are perfectly suited to be used in culture or in vivo (for nonhuman studies) for functional assays — blocking, neutralizing, activation or depletion — where the presence of azide may damage cells or exogenous endotoxin may signal or activate cells.
NA/LE
554379 Rev.3
Citations & References
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Development References (4)

  1. Abrams JS, Pearce MK.. Development of rat anti-mouse interleukin 3 monoclonal antibodies which neutralize bioactivity in vitro. J Immunol. 1988; 140(1):131-137. (Biology). View Reference
  2. Abrams JS, Roncarolo MG, Yssel H, Andersson U, Gleich GJ, Silver JE. Strategies of anti-cytokine monoclonal antibody development: immunoassay of IL-10 and IL-5 in clinical samples. Immunol Rev. 1992; 127:5-24. (Biology). View Reference
  3. Cockayne DA, Abrams JS, Nienhuis AW. Antisense RNA inhibition of hematopoietic growth factor production. Growth Factors. 1991; 5(3):171-181. (Biology). View Reference
  4. Weinstein Y, Ihle JN, Lavu S, Reddy EP. Truncation of the c-myb gene by a retroviral integration in an interleukin 3-dependent myeloid leukemia cell line. Proc Natl Acad Sci U S A. 1986; 83(14):5010-5014. (Biology). View Reference
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554379 Rev. 3

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Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims.  Comparisons are not made against non-BD technologies, unless otherwise noted.

For Research Use Only. Not for use in diagnostic or therapeutic procedures.