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BV421 Mouse Anti-Human TACTILE (CD96)
BV421 Mouse Anti-Human TACTILE (CD96)
Two-color flow cytometric analysis of TACTILE (CD96) expression on Human peripheral blood lymphocytes. The flow cytometric data from the same stained cells was reanalyzed to generate the bivariate pseudocolor density plot showing the correlated expression of TACTILE (CD96) [or Ig Isotype control staining] versus CD3 for gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa™ X-20 Cell Analyzer System and FlowJo™ software.
BV421 Mouse Anti-Human TACTILE (CD96)
Multiparameter flow cytometric analysis of TACTILE (CD96) expression on Human peripheral blood leucocytes. Human whole blood was stained with APC Mouse Anti-Human CD3 antibody (Cat No. 561811/555335/561810) and with either BD Horizon™ BV421 Mouse IgG1, κ Isotype Control (Cat No. 562438; Left Plot) or BD Horizon™ BV421 Mouse Anti-Human TACTILE (CD96) antibody (Cat No. 568858/568859; Right Plot). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The bivariate pseudocolor density plot showing the correlated expression of TACTILE (CD96) [or Ig Isotype control staining] versus side light-scatter (SSC-A) signals was 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.
Two-color flow cytometric analysis of TACTILE (CD96) expression on Human peripheral blood lymphocytes. The flow cytometric data from the same stained cells was reanalyzed to generate the bivariate pseudocolor density plot showing the correlated expression of TACTILE (CD96) [or Ig Isotype control staining] versus CD3 for gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa™ X-20 Cell Analyzer System and FlowJo™ software.
Multiparameter flow cytometric analysis of TACTILE (CD96) expression on Human peripheral blood leucocytes. Human whole blood was stained with APC Mouse Anti-Human CD3 antibody (Cat No. 561811/555335/561810) and with either BD Horizon™ BV421 Mouse IgG1, κ Isotype Control (Cat No. 562438; Left Plot) or BD Horizon™ BV421 Mouse Anti-Human TACTILE (CD96) antibody (Cat No. 568858/568859; Right Plot). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The bivariate pseudocolor density plot showing the correlated expression of TACTILE (CD96) [or Ig Isotype control staining] versus side light-scatter (SSC-A) signals was 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.
製品詳細
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BD Horizon™
hCD96; T cell-activated increased late expression protein
Human (QC Testing)
Mouse IgG1, κ
Human NK92 Cell Line
Flow cytometry (Routinely Tested)
5 µl
10225
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 and unconjugated antibody and free dye were removed.

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BD® CompBeads can be used as surrogates to assess fluorescence spillover (compensation).  When fluorochrome conjugated antibodies are bound to BD® 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 BD® CompBeads to ensure that BD® CompBeads are appropriate for your specific cellular application.

For optimal and reproducible results, BD Horizon Brilliant Stain Buffer should be used anytime BD Horizon Brilliant dyes are used in a multicolor flow cytometry panel.  Fluorescent dye interactions may cause staining artifacts which may affect data interpretation.  The BD Horizon Brilliant Stain Buffer was designed to minimize these interactions. When BD Horizon Brilliant Stain Buffer is used in in the multicolor panel, it should also be used in the corresponding compensation controls for all dyes to achieve the most accurate compensation. For the most accurate compensation, compensation controls created with either cells or beads should be exposed to BD Horizon Brilliant Stain Buffer for the same length of time as the corresponding multicolor panel. 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. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
  2. This reagent has been pre-diluted for use at the recommended Volume per Test. We typically use 1 × 10^6 cells in a 100-µl experimental sample (a test).
  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 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.
  7. 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.
  8. Human donor specific background has been observed in relation to the presence of anti-polyethylene glycol (PEG) antibodies, developed as a result of certain vaccines containing PEG, including some COVID-19 vaccines. We recommend use of BD Horizon Brilliant™ Stain Buffer in your experiments to help mitigate potential background. For more information visit https://www.bdbiosciences.com/en-us/support/product-notices.
  9. Please refer to http://regdocs.bd.com to access safety data sheets (SDS).
抗体の詳細
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NK92.39.rMAb

The NK92.39.rMAb monoclonal antibody specifically recognizes human CD96 which is also known as TACTILE (T cell activation increased late expression). CD96 is a type I membrane glycoprotein comprised of three N-terminal Ig-like extracellular domains followed by one mucin-like domain, a transmembrane region, and a cytoplasmic tail with one basic/proline rich motif, a single ITIM motif, and an YXXM motif which is also present in ICOS and CD28. CD96 is expressed at low levels on resting natural killer (NK) cells and T cells and at high levels on activated NK and T cells. CD96 is also expressed at low levels on some B cells and on some T-cell leukemia and acute myeloid leukemia cells. CD96 plays a role in the adhesive interactions of activated NK and T cells with target cells during immune responses. CD96 binds to the poliovirus receptor (CD155) that is highly expressed on some tumor cells. CD155-mediated ligation of CD96 can activate NK cell-mediated cytotoxicity.

フォーマットの詳細
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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
引用&参考文献
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Development References (3)

  1. El-Sherbiny YM, Meade JL, Holmes TD, et al. The requirement for DNAM-1, NKG2D, and NKp46 in the natural killer cell-mediated killing of myeloma cells.. Cancer Res. 2007; 67(18):8444-9. (Clone-specific). View Reference
  2. Fuchs A, Cella M, Giurisato E, Shaw AS, Colonna M. Cutting edge: CD96 (tactile) promotes NK cell-target cell adhesion by interacting with the poliovirus receptor (CD155).. J Immunol. 2004; 172(7):3994-8. (Immunogen). View Reference
  3. Toutirais O, Cabillic F, Le Friec G, et al. DNAX accessory molecule-1 (CD226) promotes human hepatocellular carcinoma cell lysis by Vgamma9Vdelta2 T cells.. Eur J Immunol. 2009; 39(5):1361-8. (Clone-specific). View Reference

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