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      FITC Mouse Anti-Human Terminal-Deoxynucleotidyl Transferase (TdT)
      Product Details
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      BD™
      TdT; DNTT; Terminal transferase; Terminal addition enzyme
      Human
      Mouse BALB/c IgG1, κ
      Purified Human TdT
      Flow cytometry
      12.5 μg/mL
      20 μL
      1791
      AB_400259
      Phosphate buffered saline with gelatin and 0.1% sodium azide.
      RUO (GMP)


      Preparation And Storage

      The FITC conjugate is supplied as 12.5 µg in 1.0 mL (12.5 µg/mL) of PBS. The PE conjugate is supplied as 6.0 µg in 1.0 mL (6.0 µg/mL) of PBS. The APC conjugate is supplied as 12.5 µg in 0.5 mL (25 µg/mL) of PBS. PBS contains gelatin and 0.1% sodium azide. Vials should be stored at 2° to 8°C. Conjugated forms should not be frozen and should be protected from prolonged exposure to light. Each reagent is stable for the period shown on the bottle label when stored as directed.

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      347194 Rev. 1
      Antibody Details
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      E17-1519

      Anti-TdT, clone E17-1519, is generated from the fusion of FO myeloma cells with spleen cells from BALB/c mice immunized with purified TdT enzyme.

      Anti–terminal-deoxynucleotidyl transferase (TdT) recognizes a 60-kilodalton (kd) polymerase, a nuclear enzyme that catalyzes the template-independent addition of nucleotides to single-stranded DNA primers. It has been reported that TdT is involved in the regulation or translocation or both of DNA and gene rearrangement during normal T- and B-cell development.

      347194 Rev. 1
      Format Details
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      FITC
      Fluorescein (FITC) is part of the BD blue family of dyes. This is a small organic fluorochrome with an excitation maximum (Ex Max) at 494-nm and an emission maximum (Em Max) at 518-nm. FITC is designed to be excited by the Blue laser (488-nm) and detected using an optical filter centered near 520 nm (e.g., a 530/30-nm bandpass filter). Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye.
      altImg
      FITC
      494 nm
      518 nm
      347194 Rev.1
      Citations & References
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      View product citations for antibody "347194" on CiteAb

      Development References (7)

      1. Fuller SA, Phillips A, Coleman MS. Affinity purification and refined structural characterization of terminal deoxyribonucleotidyl transferase. Biochem J. 1985; 231:105-113. (Biology).
      2. Gore SD, Kastan MB, Civin CI. Normal human bone marrow precursors that express terminal deoxynucleotidyl transferase include T-cell precursors and possible lymphoid stem cells.. Blood. 1991; 77(8):1681-90. (Biology). View Reference
      3. Horvatinovich JM, Sparks SD, Borowitz MJ. Detection of terminal deoxynucleotidyl transferase by flow cytometry: a three color method. Cytometry. 1994; 18:228-230. (Biology).
      4. Komori T, Okada A, Stewart V, Alt FW. Lack of N regions in antigen receptor variable regions of TdTdeficient lymphocytes. Science. 1993; 261:1171-1175. (Biology).
      5. Landau NR, Schatz DG, Rosa M, Baltimore D. Increased frequency of N-region insertion in a murine pre–B-cell line infected with a terminal deoxynucleotidyl transferase retroviral expression vector. Mol Cell Biol. 1987; 7:3237-3243. (Biology).
      6. Paietta E, Meenan B, Heavey C, Thomas D. Detection of terminal transferase in acute myeloid leukemia by flow cytometry. Cytometry. 1994; 16:256-261. (Biology).
      7. Roma AO, Kutok JL, Shaheen G, Dorfman DM. A novel, rapid, multiparametric approach for flow cytometric analysis of intranuclear terminal deoxynucleotidyl transferase. Am J Clin Pathol. 1999; 112:343-348. (Biology).
      View All (7) View Less
      347194 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. 

       

      Although not required, these products are manufactured in accordance with Good Manufacturing Practices.