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Two-color flow cytometric analysis of ZBTB7B (Th-POK) expression in human peripheral blood mononuclear cells. PBMCs were surface stained with Alexa Fluor® 488 Mouse Anti-Human CD4 antibody (Cat. No. 557695). The cells were then washed, fixed, and permeabilized using the BD Pharmingen™ Transcription Factor Buffer Set (Cat. No. 562574/562725) and stained with either PE Mouse IgG1, κ Isotype Control (Cat. No. 554680) or PE Mouse Anti-Human ZBTB7B (ThPOK) antibody. The two-color flow cytometric contour plots showing the correlated expression of ZBTB7B (ThPOK) [or Ig Isotype Control] versus CD4 were derived from gated events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometric analysis was performed using a BD LSR Fortessa™ X-20 Flow Cytometer System.
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BD Pharmingen™ PE Mouse Anti-Human ZBTB7B (ThPOK)
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- 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).
- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
- 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.
- Source of all serum proteins is from USDA inspected abattoirs located in the United States.
- Alexa Fluor® is a registered trademark of Molecular Probes, Inc., Eugene, OR.
- For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
- An isotype control should be used at the same concentration as the antibody of interest.
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The 6/hcKrox monoclonal antibody specifically recognizes human Th Inducing POZ-Kruppel Factor (ThPOK) which is also known as, cKrox or hcKrox. ThPOK is encoded by ZBTB7B (Zinc finger and BTB domain-containing protein 7B) and is a member of the POK/ZBT family of transcription regulators that play roles in lymphocyte development and the regulation of type I collagen genes. ThPOK expression is upregulated during the differentiation of CD4+ T helper cells but not CD8+ T cells. It indirectly increases the expression of CD4 in developing T cells by antagonizing Runx-3-mediated CD4 repression. ThPOK is also expressed in NKT and γδ T cells.

Development References (3)
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Heegaard AM, Gehron Robey P, Vogel W. Functional characterization of the human biglycan 5'-flanking DNA and binding of the transcription factor c-Krox. J Bone Miner Res. 1997; 12(12):2050-2060. (Biology). View Reference
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Peterkofsky B, Gosiewska A, Singh K, Pearlman S, Mahmoodian F. Species differences in cis-elements of the proalpha1(I) procollagen promoter and their binding proteins. J Cell Biochem. 1999; 73(3):408-422. (Biology). View Reference
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Widom RL, Culic I, Lee JY, Korn JH. Cloning and characterization of hcKrox, a transcriptional regulator of extracellular matrix gene expression. Gene. 1997; 198(1-2):407-420. (Biology). View Reference
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