This enzyme is essential for vertebrate adaptive immune system, as it helps to generate enormous quantities of different specific B cell receptor and T cell receptor variants. Its ability to elongate single-stranded DNA is also being used e.g. for identification of fragmented DNA in apoptotic cells, or for synthesis of oligonucleotides. However, TdT is also an important marker in the diagnosis of leukemias. As it is expressed only in certain phase of B cell and T cell development, when the rearrangement of immune receptor genes occurs, it can be used for distinguishing between premature and mature lymphoid cells, both in flow cytometry and immunohistochemistry. For example it is a marker in the diagnosis of acute lymphoblastic leukemia, and its distinguishing from Burkitt lymphoma and other lymphoid malignancies. The mouse monoclonal antibody 41A, recognizing human TdT, is suitable for immunohistochemistry (paraffin sections), flow cytometry, Western blotting, and ELISA. Currently available formate: Anti-Hu TdT Purified FIG. 1: Separation of REH cells stained with anti-human TdT (41A) purified antibody (concentration in the sample 0.9 μg/ml, GAM APC, red-filled) from REH cells unstained by primary antibody (GAM APC, black-dashed) in flow cytometry analysis (intracellular staining).
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Anti-human CD38 clones HB7 and HIT2 were compared regarding their reactivity with particular blood cell populations.
Here we present two basic systems of biotin detection, namely anti-biotin monoclonal antibody and streptavidin conjugates.
Anti-human CD25 clones MEM-181, B1.49.9, 2A3, BC96, CD25-4E3, and CD25-3G10 were compared regarding their reactivity with particular blood cell populations.