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PE Mouse Anti-Human Terminal-Deoxynucleotidyl Transferase (TdT)
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TdT; DNTT; Terminal transferase; Terminal addition enzyme
Mouse BALB/c IgG1, κ
Purified Human TdT
Flow cytometry
6.0 μg/mL
20 μL
Phosphate buffered saline with gelatin and 0.1% sodium azide.

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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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.

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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.
Yellow-Green 488 nm, 532 nm, 561 nm
496 nm, 566 nm
576 nm
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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).
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