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BV421 Rat Anti-Mouse CD354 (TREM-1)
BV421 Rat Anti-Mouse CD354 (TREM-1)
Two-color flow cytometric analysis of CD354 (TREM-1) expression on mouse splenocytes. BALB/c mouse splenic leucocytes were preincubated with Purified Rat Anti-Mouse CD16/CD32 (Mouse BD Fc Block™) (Cat. No. 553141 or 553142). The cells were then stained with PE Rat Anti-Mouse Ly-6G and Ly-6C (Gr-1) (Cat No. 553128 or 561084), and either BD Horizon™ BV421 Rat IgG2a, κ Isotype Control (Cat. No. 562602; Left Plot) or BD OptiBuild™ BV421 Rat Anti-Mouse CD354 (TREM-1) (Cat. No. 747899; Right Plot) at 0.25 µg/test. The pseudocolor dot plots showing CD354 (TREM-1) [or Ig Isotype control] staining versus Gr-1 were derived from gated events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa™ X-20 Cell Analyzer System and FlowJo™ software. The above is qualification data only and does not represent a specific OptiBuild™ lot. \\
Two-color flow cytometric analysis of CD354 (TREM-1) expression on mouse splenocytes. BALB/c mouse splenic leucocytes were preincubated with Purified Rat Anti-Mouse CD16/CD32 (Mouse BD Fc Block™) (Cat. No. 553141 or 553142). The cells were then stained with PE Rat Anti-Mouse Ly-6G and Ly-6C (Gr-1) (Cat No. 553128 or 561084), and either BD Horizon™ BV421 Rat IgG2a, κ Isotype Control (Cat. No. 562602; Left Plot) or BD OptiBuild™ BV421 Rat Anti-Mouse CD354 (TREM-1) (Cat. No. 747899; Right Plot) at 0.25 µg/test. The pseudocolor dot plots showing CD354 (TREM-1) [or Ig Isotype control] staining versus Gr-1 were derived from gated events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa™ X-20 Cell Analyzer System and FlowJo™ software. The above is qualification data only and does not represent a specific OptiBuild™ lot. \\
Product Details
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BD OptiBuild™
CD354; TREM-1; Trem1
Mouse (Tested in Development)
Rat IgG2a, κ
Mouse TREM-1 (Ala21-Ser202) Recombinant Protein
Flow cytometry (Qualified)
0.2 mg/ml
AB_2872361
Aqueous buffered solution containing ≤0.09% sodium azide.
RUO


Preparation And Storage

Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze. The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. The antibody was conjugated to the dye under optimum conditions that minimize unconjugated dye and antibody.

Recommended Assay Procedures

BD™ CompBeads can be used as surrogates to assess fluorescence spillover (Compensation).  When fluorochrome conjugated antibodies are bound to CompBeads, they have spectral properties very similar to cells.   However, for some fluorochromes there can be small differences in spectral emissions compared to cells, resulting in spillover values that differ when compared to biological controls.  It is strongly recommended that when using a reagent for the first time, users compare the spillover on cells and CompBead to ensure that BD Comp beads are appropriate for your specific cellular application.

For optimal and reproducible results, BD Horizon Brilliant Stain Buffer should be used anytime two or more BD Horizon Brilliant dyes are used in the same experiment.  Fluorescent dye interactions may cause staining artifacts which may affect data interpretation.  The BD Horizon Brilliant Stain Buffer was designed to minimize these interactions.  More information can be found in the Technical Data Sheet of the BD Horizon Brilliant Stain Buffer (Cat. No. 563794/566349) or the BD Horizon Brilliant Stain Buffer Plus (Cat. No. 566385).

Product Notices

  1. The production process underwent stringent testing and validation to assure that it generates a high-quality conjugate with consistent performance and specific binding activity. However, verification testing has not been performed on all conjugate lots.
  2. Researchers should determine the optimal concentration of this reagent for their individual applications.
  3. An isotype control should be used at the same concentration as the antibody of interest.
  4. 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.
  5. For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
  6. BD Horizon Brilliant Stain Buffer is covered by one or more of the following US patents: 8,110,673; 8,158,444; 8,575,303; 8,354,239.
  7. BD Horizon Brilliant Violet 421 is covered by one or more of the following US patents: 8,158,444; 8,362,193; 8,575,303; 8,354,239.
  8. Pacific Blue™ is a trademark of Molecular Probes, Inc., Eugene, OR.
  9. Please refer to http://regdocs.bd.com to access safety data sheets (SDS).
  10. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
747899 Rev. 2
Antibody Details
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174031

The 174031 monoclonal antibody specifically recognizes CD354 which is also known as Triggering receptor expressed on myeloid cells 1 (TREM-1) or Triggering receptor expressed on monocytes 1. CD354 (TREM-1) is a ~30 kDa single-pass type I transmembrane glycoprotein that is encoded by Trem1 which belongs to the V-set domain containing family within the Ig superfamily. CD354 (TREM-1) can associate with DAP12, an adaptor protein that contains an immunoreceptor tyrosine-based activation motif (ITAM), to deliver an activating signal intracellularly. It is expressed on neutrophils and some monocytes and macrophages with upregulated expression triggered in response to bacterial lipopolysaccharide (LPS) exposure. CD354 (TREM-1) appears to play important roles in inflammation and septic shock by inducing the production of pro-inflammatory cytokines and chemokines including TNF and MCP-1/CCL2. A soluble form of TREM-1 may be released by cells and serve as an inhibitor of cell surface TREM-1 function.

The antibody was conjugated to BD Horizon BV421 which is part of the BD Horizon Brilliant™ Violet family of dyes. With an Ex Max near 407 nm and Em Max near 421 nm, BD Horizon BV421 can be excited by the violet laser (405 nm) and detected with a 450/50 nm filter. BD Horizon BV421 conjugates are very bright, often exhibiting a 10 fold improvement in brightness compared to Pacific BlueTM conjugates. Due to nearly identical excitation and emission properties but different spillover characteristics, BD Horizon BV421, Pacific Blue, and BD Horizon V450 cannot be used simultaneously.

747899 Rev. 2
Format Details
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BV421
The BD Horizon Brilliant Violet™ 421 (BV421) Dye is part of the BD Horizon Brilliant Violet™ family of dyes. This polymer-technology based dye has an excitation maximum (Ex Max) of 407-nm and an emission maximum (Em Max) at 423-nm. Driven by BD innovation, BV421 is designed to be excited by the violet laser (405-nm) and detected using an optical filter centered near 420-nm (e.g., a 431/28-nm or 450/50-nm bandpass filter). BV421 is an ideal alternative for V450 as it is approximately ten times brighter with less spillover into the BV510/V500 detector. Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye.
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BV421
Violet 405 nm
407 nm
423 nm
747899 Rev.2
Citations & References
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Development References (3)

  1. Bouchon A, Dietrich J, Colonna M. Cutting edge: inflammatory responses can be triggered by TREM-1, a novel receptor expressed on neutrophils and monocytes. J Immunol. 2000; 164(10):4991-4995. (Biology). View Reference
  2. Gibot S, Massin F, Marcou M, et al. TREM-1 promotes survival during septic shock in mice.. Eur J Immunol. 2007; 37(2):456-66. (Clone-specific: Flow cytometry). View Reference
  3. Yuan Z, Syed MA, Panchal D, et al. Triggering receptor expressed on myeloid cells 1 (TREM-1)-mediated Bcl-2 induction prolongs macrophage survival.. J Biol Chem. 2014; 289(21):15118-29. (Clone-specific: Flow cytometry). View Reference
747899 Rev. 2

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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.