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PE Hamster Anti-Mouse CD120b
PE Hamster Anti-Mouse CD120b
Expression of cell surface p75 TNFR by BALB/c lymph node T cells. BALB/c lymph node cells were preincubated (~15 min., 4°C) with purified 2.4G2 antibody [rat anti-mouse CD16 (FcγIII)/CD32 (FcγII); Cat. No. 553142; 1 µg antibody/10e6 cells] to block Fc receptor-mediated nonspecific staining by staining antibodies. The cells were stained (1 hr., 4°C) with R-PE conjugated TR7589 antibody (1 µg mAb/10e6 cells; Cat. No. 550086). The cells were washed and were incubated with FITC- RA3-6B2/B220 (Cat. No. 553088; 0.06 µg mAb/10e6 cells), and were washed in preparation for flow cytometric analysis with a FACScan™ Flow Cytometer. The immunofluorescent staining patterns for cells stained with either R-PE conjugated TR75-89 antibody (filled histogram) or streptavidin-PE (background staining; empty histogram) is shown. The histograms were generated from reanalyzed flow cytometric data files that were gated for FITC-negative events with the light-scattering characteristics of lymphocytes, i.e., B220-negative lymph node T cells.
Expression of cell surface p75 TNFR by BALB/c lymph node T cells. BALB/c lymph node cells were preincubated (~15 min., 4°C) with purified 2.4G2 antibody [rat anti-mouse CD16 (FcγIII)/CD32 (FcγII); Cat. No. 553142; 1 µg antibody/10e6 cells] to block Fc receptor-mediated nonspecific staining by staining antibodies. The cells were stained (1 hr., 4°C) with R-PE conjugated TR7589 antibody (1 µg mAb/10e6 cells; Cat. No. 550086). The cells were washed and were incubated with FITC- RA3-6B2/B220 (Cat. No. 553088; 0.06 µg mAb/10e6 cells), and were washed in preparation for flow cytometric analysis with a FACScan™ Flow Cytometer. The immunofluorescent staining patterns for cells stained with either R-PE conjugated TR75-89 antibody (filled histogram) or streptavidin-PE (background staining; empty histogram) is shown. The histograms were generated from reanalyzed flow cytometric data files that were gated for FITC-negative events with the light-scattering characteristics of lymphocytes, i.e., B220-negative lymph node T cells.
Product Details
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BD Pharmingen™
Tnfrsf1b; Tnfr2; TNF-R2; TNFR p75; TNFRII; TNF-R-II; TNFBR
Mouse (QC Testing)
Armenian Hamster IgG1, λ3
Mouse Type II TNFR
Flow cytometry (Routinely Tested)
0.2 mg/ml
AB_393556
Aqueous buffered solution containing ≤0.09% sodium azide.
RUO


Preparation And Storage

The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. The antibody was conjugated with R-PE under optimum conditions, and unconjugated antibody and free PE were removed. Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze.

Recommended Assay Procedures

Immunofluorescent Staining and Flow Cytometric Analysis: The R-PE conjugated form of TR75-89 (Cat. No. 550086) can be used for the immunofluorescent staining (≤ 1 µg antibody/10e6 cells) and flow cytometric analysis of normal mouse cells or cell lines to measure their expressed levels of p75 TNFR. An appropriate R-PE-conjugated immunoglobulin isotype control is clone G235-2356 (Cat. No. 554711).

Note: TR75-89 is a nonblocking antibody that can be used for the unobstructed immunofluorescent staining and flow cytometric analysis of cells in systems where ligands (e.g., TNF) for p75 TNF receptors are present. Based on our testing results (data not shown), the presence of exogenous recombinant mouse TNF (Cat. No. 554589) at levels ≤ 1 µg per 10e6 cells was insufficient to inhibit the binding of TR75-89 to L929 cells that express p75 TNFR (at 0.25 µg antibody/10e6 cells). Please note also that as a consequence of in vivo or in vitro activation, cell surface p75 TNFR can either be shed by cells or transiently expressed at higher levels. As a result, cellular activation can affect the cells overall expressed level of surface p75 TNFR.

IP: The TR75-89 antibody has been reported to be useful for the immunoprecipitation of p75 TNFR from lysates of mouse Meth A fibrosarcoma cells. Please note that this application is not routinely tested at BD Biosciences Pharmingen.

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.
  3. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
  4. Although hamster immunoglobulin isotypes have not been well defined, BD Biosciences Pharmingen has grouped Armenian and Syrian hamster IgG monoclonal antibodies according to their reactivity with a panel of mouse anti-hamster IgG mAbs. A table of the hamster IgG groups, Reactivity of Mouse Anti-Hamster Ig mAbs, may be viewed at http://www.bdbiosciences.com/documents/hamster_chart_11x17.pdf.
550086 Rev. 1
Antibody Details
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TR75-89

The TR75-89 monoclonal antibody specifically binds to the extracellular region of CD120b, the 75 kDa receptor for the mouse cytokines, tumor necrosis factor (TNF, aka TNF-α) and lymphotoxin-alpha (LT-α, aka lymphotoxin, TNF-β). This receptor, referred to as the p75 or Type II Tumor Necrosis Factor Receptor (TNFRII), or TNFRSF1B, is expressed by a variety of cell lines and normal cell types including T cells, monocytes, macrophages, and neutrophils. Resting B cells express low or undetectable levels of TNFRII whereas mature erythrocytes are uniformly negative for TNFRII expression. In addition, the TR75-89 antibody can bind to a soluble, truncated form of the mouse Type II TNFR that is shed by cells in response to certain stimuli, e.g., cells treated with LPS or TNF. The in vivo administration of nonblocking, nonagonistic TR75-89 antibody reportedly results in the linear accumulation of shed, soluble forms of p75 TNFR in the circulation. The TR75-89 antibody does not recognize the 55 kDa (p55) Type I TNFR (aka, CD120a). TR75-89 does not block the binding and does not neutralize the bioactivity of the TNF ligand on L929 target cell populations that express p75 (and p55) TNFR. The immunogen used to generate the TR75-89 hybridoma was a purified, soluble extracellular domain of the mouse Type II TNFR.

This antibody is routinely tested by flow cytometric analysis. Other applications were tested at BD Biosciences Pharmingen during antibody development only or reported in the literature.

550086 Rev. 1
Format Details
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PE
R-Phycoerythrin (PE), is part of the BD family of Phycobiliprotein dyes. This fluorochrome is a multimeric fluorescent phycobiliprotein with excitation maximum (Ex Max) of 496 nm and 566 nm and an emission maximum (Em Max) at 576 nm. PE is designed to be excited by the Blue (488 nm), Green (532 nm) and Yellow-Green (561 nm) lasers and detected using an optical filter centered near 575 nm (e.g., a 575/26-nm bandpass filter). As PE is excited by multiple lasers, this can result in cross-laser excitation and fluorescence spillover on instruments with various combinations of Blue, Green, and Yellow-Green lasers. Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye.
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PE
Yellow-Green 488 nm, 532 nm, 561 nm
496 nm, 566 nm
576 nm
550086 Rev.1
Citations & References
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Development References (3)

  1. Pinckard JK, Sheehan KC, Arthur CD, Schreiber RD. Constitutive shedding of both p55 and p75 murine TNF receptors in vivo. J Immunol. 1997; 158(8):3869-3873. (Clone-specific). View Reference
  2. Pinckard JK, Sheehan KC, Schreiber RD. Ligand-induced formation of p55 and p75 tumor necrosis factor receptor heterocomplexes on intact cells. J Biol Chem. 1997; 272(16):10784-10789. (Clone-specific: Immunoprecipitation). View Reference
  3. Sheehan KC, Pinckard JK, Arthur CD, Dehner LP, Goeddel DV, Schreiber RD. Monoclonal antibodies specific for murine p55 and p75 tumor necrosis factor receptors: identification of a novel in vivo role for p75. J Exp Med. 1995; 181(2):607-617. (Clone-specific). View Reference
550086 Rev. 1

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Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described


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.

Refer to manufacturer's instructions for use and related User Manuals and Technical Data Sheets before using this product as described.

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.