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PE Mouse Anti-Human BCMA (CD269)
PE Mouse Anti-Human BCMA (CD269)

Flow cytometric analysis of BCMA (CD269) expression on Human U266 cells. Cells from the Human U266 (Myeloma, ATCC® TIB-196™) cell line were preincubated with Human BD Fc Block™ (Cat. No. 564219/564220) and stained with either PE Mouse IgG1, κ Isotype Control (Cat. No. 554680; dashed line histogram) or PE Mouse Anti-BCMA (CD269) antibody (Cat. No. 570546/570547; solid line histograms) at 1 ug/test. DAPI (4',6-Diamidino-2-Phenylindole, Dihydrochloride) Solution (Cat. No. 564907) was added to cells right before analysis. The fluorescence histogram showing BCMA (CD269) expression] or [Ig Isotype control staining] was derived from gated events with the forward and side light-scatter characteristics of viable (DAPI-negative) cells. Flow cytometry and data analysis were performed using a BD Celesta™ Cell Analyzer System and FlowJo™ Software. Data shown on this Technical Data Sheet are not lot specific.

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BD Pharmingen™
B-cell maturation protein; BCM; TNFRSF17
Human (QC Testing)
Mouse BALB/c IgG1, κ
Human BCMA Ectodomain-Mouse IgG Fc
Flow cytometry (Routinely Tested)
0.2 mg/ml
608
AB_3685832
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 to the dye under optimum conditions and unconjugated antibody and free dye were removed. Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze.

推奨アッセイ手順

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.

Product Notices

  1. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
  2. 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.
  3. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
  4. For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
  5. An isotype control should be used at the same concentration as the antibody of interest.
  6. Please refer to http://regdocs.bd.com to access safety data sheets (SDS).
  7. For U.S. patents that may apply, see bd.com/patents.

データシート

570547 Rev. 1
抗体の詳細
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19F2.rMAb

19F2.rMAb is a recombinant monoclonal antibody derived from 19F2 hybridoma cells. The 19F2.rMAb specifically recognizes B cell maturation antigen (BCMA) which is also known as CD269. CD269 (BCMA) is an ~27 kDa type III transmembrane glycoprotein that is encoded by TNFRSF17 (TNF receptor superfamily member 17). The extracellular domain of this receptor has one TNFR-Cys repeat and is followed by a transmembrane region and a cytoplasmic domain. CD269 (BCMA) is expressed as a homotrimer on germinal center B cells, plasmablasts, and plasma cells. It is expressed at elevated levels in B cell malignancies including increased expression by malignant plasma cells in multiple myeloma and has been associated with certain autoimmune diseases like systemic lupus erythematosus. This receptor binds to and transduces intracellular signaling in response to its ligands, CD257 (aka, BAFF and Blys) and CD256 (APRIL). CD269 (BCMA) functions as a B cell maturation factor that is essential for the survival of long-lived bone marrow plasma cells. A soluble form of CD269 (BCMA) is generated by γ-secretase that can regulate plasma cell survival and differentiation. Soluble CD269 (BCMA) may also act as a decoy receptor that can regulate the availability of BAFF and APRIL ligands.

570547 Rev. 1
フォーマットの詳細
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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.
altImg
PE
Yellow-Green 561 nm
496 nm, 566 nm
576 nm
570547 Rev.1
引用&参考文献
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Development References (11)

  1. Avery DT, Ellyard JI, Mackay F, Corcoran LM, Hodgkin PD, Tangye SG. Increased expression of CD27 on activated human memory B cells correlates with their commitment to the plasma cell lineage.. J Immunol. 2005; 174(7):4034-42. (Biology). View Reference
  2. Avery DT, Kalled SL, Ellyard JI, et al. BAFF selectively enhances the survival of plasmablasts generated from human memory B cells.. J Clin Invest. 2003; 112(2):286-97. (Biology). View Reference
  3. Bae J, Samur M, Richardson P, Munshi NC, Anderson KC. Selective targeting of multiple myeloma by B cell maturation antigen (BCMA)-specific central memory CD8+ cytotoxic T lymphocytes: immunotherapeutic application in vaccination and adoptive immunotherapy.. Leukemia. 2019; 33(9):2208-2226. (Clone-specific: Flow cytometry). View Reference
  4. Berahovich R, Zhou H, Xu S, et al. CAR-T Cells Based on Novel BCMA Monoclonal Antibody Block Multiple Myeloma Cell Growth.. Cancers (Basel). 2018; 10(9):323. (Clone-specific: Flow cytometry). View Reference
  5. Carpenter RO, Evbuomwan MO, Pittaluga S, et al. B-cell maturation antigen is a promising target for adoptive T-cell therapy of multiple myeloma.. Clin Cancer Res. 2013; 19(8):2048-60. (Biology). View Reference
  6. Friedman KM, Garrett TE, Evans JW, et al. Effective Targeting of Multiple B-Cell Maturation Antigen-Expressing Hematological Malignances by Anti-B-Cell Maturation Antigen Chimeric Antigen Receptor T Cells.. Hum Gene Ther. 2018; 29(5):585-601. (Clone-specific: Flow cytometry). View Reference
  7. Laurent SA, Hoffmann FS, Kuhn PH, et al. γ-Secretase directly sheds the survival receptor BCMA from plasma cells.. Nat Commun. 2015; 6:7333. (Biology). View Reference
  8. Lee L, Draper B, Chaplin N, et al. An APRIL-based chimeric antigen receptor for dual targeting of BCMA and TACI in multiple myeloma.. Blood. 2018; 131(7):746-758. (Clone-specific: Flow cytometry). View Reference
  9. Nobari ST, Nojadeh JN, Talebi M. B-cell maturation antigen targeting strategies in multiple myeloma treatment, advantages and disadvantages.. J Transl Med. 2022; 20(1):82. (Biology). View Reference
  10. Schuh E, Musumeci A, Thaler FS, et al. Human Plasmacytoid Dendritic Cells Display and Shed B Cell Maturation Antigen upon TLR Engagement.. J Immunol. 2017; 198(8):3081-3088. (Biology). View Reference
  11. Zola H, Swart B, Nicholson I, Voss E. CD269. In: Zola H. Leukocyte and stromal cell molecules : the CD markers. Hoboken, N.J.: Wiley-Liss; 2007: p. 430. View Reference
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570547 Rev. 1

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