Recombinant Mouse Zinc finger and BTB domain-containing protein 7B (Zbtb7b)

Code CSB-YP731047MO
MSDS
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Source Yeast
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Code CSB-EP731047MO
MSDS
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Source E.coli
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Code CSB-EP731047MO-B
MSDS
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Source E.coli
Conjugate Avi-tag Biotinylated
E. coli biotin ligase (BirA) is highly specific in covalently attaching biotin to the 15 amino acid AviTag peptide. This recombinant protein was biotinylated in vivo by AviTag-BirA technology, which method is BriA catalyzes amide linkage between the biotin and the specific lysine of the AviTag.
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Code CSB-BP731047MO
MSDS
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Source Baculovirus
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Code CSB-MP731047MO
MSDS
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Source Mammalian cell
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Product Details

Purity
>85% (SDS-PAGE)
Target Names
Zbtb7b
Uniprot No.
Alternative Names
Zbtb7b; Thpok; Zfp67; Zinc finger and BTB domain-containing protein 7B; Krueppel-related zinc finger protein cKrox; c-Krox; T-helper-inducing POZ/Krueppel-like factor; Zinc finger protein 67; Zfp-67; Zinc finger protein Th-POK
Species
Mus musculus (Mouse)
Expression Region
1-544
Target Protein Sequence
MGSPEDDLIG IPFPDHSSEL LSCLNEQRQL GHLCDLTIRT QGLEYRTHRA VLAACSHYFK KLFTEGGGGT VMGTGGGGTA SGGAGAGVCE LDFVGPEALG ALLEFAYTAT LTTSSANMPA VLQAARLLEI PCVIAACMEI LQGSGLEAPS PDEDDCERAR QYLEAFATAT TTASTSGMPN GEDSPPQVPL LPPPPPPPRP VARRSRKPRK AFLQTKGARA NHLVPEAPTV LTHPLTYEEE EMVGRLGNSG GSGLGDSYSP PTGAASPAEG PLNYEVFEGE EEEEEMAYPP GYGLAQSNEP SLSPEELGSD EDPIDPDLMA YLSSLHQDAL TPGLDGQDKL VRKRRSQMPQ ECPVCHKIIH GAGKLPRHMR THTGEKPFAC EVCGVRFTRN DKLKIHMRKH TGERPYSCPH CPARFLHSYD LKNHMHLHTG DRPYECHLCH KAFAKEDHLQ RHLKGQNCLE VRTRRRRKDD VAAPHYPPPS TTTSSPAGLD LSNGHLDTFH LSLARFWEQS ATTGPPVTTQ GPPEEEEEEG TPTTPQAEGA MESS
Protein Length
full length protein
Tag Info
Tag type will be determined during the manufacturing process.
The tag type will be determined during production process. If you have specified tag type, please tell us and we will develop the specified tag preferentially.
Form
Lyophilized powder
Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.
Buffer before Lyophilization
Tris/PBS-based buffer, 6% Trehalose, pH 8.0
Reconstitution
We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
Troubleshooting and FAQs
Storage Condition
Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
Shelf Life
The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself.
Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
Lead Time
Delivery time may differ from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Note: All of our proteins are default shipped with normal blue ice packs, if you request to ship with dry ice, please communicate with us in advance and extra fees will be charged.
Notes
Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
Datasheet
Please contact us to get it.

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Target Background

Function
Transcription regulator that acts as a key regulator of lineage commitment of immature T-cell precursors. Exerts distinct biological functions in the mammary epithelial cells and T cells in a tissue-specific manner. Necessary and sufficient for commitment of CD4 lineage, while its absence causes CD8 commitment. Development of immature T-cell precursors (thymocytes) to either the CD4 helper or CD8 killer T-cell lineages correlates precisely with their T-cell receptor specificity for major histocompatibility complex class II or class I molecules, respectively. Cross-antagonism between ZBTB7B and CBF complexes are determinative to CD4 versus CD8 cell fate decision. Suppresses RUNX3 expression and imposes CD4+ lineage fate by inducing the SOCS suppressors of cytokine signaling. induces, as a transcriptional activator, SOCS genes expression which represses RUNX3 expression and promotes the CD4+ lineage fate. During CD4 lineage commitment, associates with multiple sites at the CD8 locus, acting as a negative regulator of the CD8 promoter and enhancers by epigenetic silencing through the recruitment of class II histone deacetylases, such as HDAC4 and HDAC5, to these loci. Regulates the development of IL17-producing CD1d-restricted naural killer (NK) T cells. Also functions as an important metabolic regulator in the lactating mammary glands. Critical feed-forward regulator of insulin signaling in mammary gland lactation, directly regulates expression of insulin receptor substrate-1 (IRS-1) and insulin-induced Akt-mTOR-SREBP signaling. Transcriptional repressor of the collagen COL1A1 and COL1A2 genes. May also function as a repressor of fibronectin and possibly other extracellular matrix genes. Potent driver of brown fat development, thermogenesis and cold-induced beige fat formation. Recruits the brown fat lncRNA 1 (Blnc1):HNRNPU ribonucleoprotein complex to activate thermogenic gene expression in brown and beige adipocytes.
Gene References into Functions
  1. Zbtb7b recruits the brown fat Blnc1/heterogeneous nuclear ribonucleoprotein U (hnRNPU) ribonucleoprotein complex to activate thermogenic gene expression in adipocytes. PMID: 28784777
  2. Th-POK functions as an important feed-forward regulator of insulin signaling in mammary gland lactation. PMID: 29420538
  3. epigenetic regulation through microRNA-133b-regulated Th-POK expression and signals provided by dendritic cells are fundamental for thymic NKT17 cell differentiation PMID: 27605013
  4. this study shows that Thpok and LRF are redundantly required to maintain the size and functions of the postthymic Treg pool PMID: 28754678
  5. Together, these results suggest a novel mechanism regulating endothelial PATZ1 expression based on the down-regulation of miR-24 expression caused by hyperglycemia. Interfering with PATZ1 expression via miRNAs or miRNA mimics could potentially represent a new way to target endothelial PATZ1-dependent signaling of vascular dysfunction in diabetes. PMID: 27983982
  6. Runx3 is crucial for the phenotypic and functional changes observed in ThPok-deficient invariant natural killer T cells. PMID: 24561456
  7. present evidence that ectopic ThPOK expression gives rise to a preleukemic and self-perpetuating DN4 lymphoma precursor population PMID: 26056302
  8. Data indicate that transcription factors Thpok and LRF redundantly maintain CD4+ lineage integrity. PMID: 25129370
  9. induction of SOCS-encoding genes is the main mechanism by which ThPOK imposes the CD4(+) lineage fate in the thymus PMID: 24880459
  10. The role of TCF-1 and LEF-1 in the CD4-versus-CD8 lineage 'choice' was mediated in part by direct positive regulation of the transcription factor Th-POK PMID: 24836425
  11. These findings imply that long-lasting T-cell receptor signals are needed to establish stable Thpok expression activity to commit to helper T-cell fate. PMID: 23481257
  12. Gata3 promotes Cd4 expression in Thpok-deficient thymocytes. PMID: 23310955
  13. Data indicate that Valpha14 invariant natural killer T (Valpha14i NKT) cells from Th-POK-mutant helper deficient (hd/hd) mice have increased transcripts of genes normally expressed by Th17 and NKT17 cells. PMID: 23034280
  14. ZBTB7B is a critical factor genetically predetermining the balance of effector subsets within the NKT cell population. PMID: 23105140
  15. Th-POK and Runx3 transcription factors are reciprocally involved in the control of G1-phase progression, on which they exert their functions dependently. PMID: 23018457
  16. T cells lacking Thpok, which only displayed LRF-dependent functions, contributed to multiple effector responses, both in vitro and in vivo, with the notable exception of Th2 cell responses that control extracellular parasites PMID: 23041065
  17. comparing the promoter regions of the Th-POK gene between human and mouse, the region 3600 base pairs upstream from the transcription initiation site of the Th-POK gene was highly conserved PMID: 20847520
  18. required for the differentiation of CD1d-restricted CD4+ NKT cells PMID: 20706986
  19. impairment of Lck-mediated CD4 coreceptor signaling by Nef is an important in vivo mechanism of HIV-1 pathogenesis PMID: 20810990
  20. Data show that ThPOK expression in gammadelta thymocytes is regulated by TCR signalling, that ThPOK is an important mediator of gammadelta T cell development/maturation, and that development of some gammadelta T cells depends on TCR engagement/signalling. PMID: 20551904
  21. Broad-complex and BTB-ZF gene ThPOK is a member of the tramtrack bric-a;-brac (BTB)-poxvirus-zinc finger family of transcription factors and is important for the phenotype of promyelocytic leukemia zinc finger (PLZF)-expressing gamma delta T cells. PMID: 20038637
  22. a point mutation in the zinc finger transcription factor Th-POK (T-helper-inducing POZ/Kruppel-like factor) is responsible for redirection of class-II-restricted thymocytes to the CD8 lineage in helper-deficient mice [Th-POK] PMID: 15729333
  23. Th-POK directs CD4 lineage differentiation during intrathymic T-cell positive selection. PMID: 15750595
  24. Role of Th-POK in CD4:CD8 lineage commitment PMID: 16448546
  25. cKrox transduction into CD8 T cells inhibits their expression of CD8 and cytotoxic effector genes and impairs their cytotoxic activity, and that it promotes expression of helper-specific genes, although not of CD4 itself. PMID: 17296789
  26. findings demonstrate that the transcription factor Zbtb7b promotes CD4 expression by antagonizing Runx-mediated CD4 repression PMID: 17878336
  27. Th-POK expression and genetic programming for T helper cell development are actively inhibited by Runx-dependent silencer activity, allowing for cytotoxic T cell differentiation PMID: 18258917
  28. we investigate the regulation of ThPOK expression and its subsequent control of CD4+ T cell commitment PMID: 18342007
  29. GATA-3 and ThPOK have essential and nonredundant functions during early CD4+ cell differentiation before lineage commitment PMID: 18776904
  30. ThPOK may not be essential for specification of the CD4 lineage PMID: 18776905
  31. inefficient upregulation of ThPOK resulted in the transdifferentiation of helper lineage-specified cells into the cytotoxic T cell lineage. PMID: 18776907
  32. a key function of Zbtb7b in the mature CD4+ T cell compartment is to repress CD8-lineage gene expression. PMID: 19062319
  33. Review summarizes recent advances on the regulatory function of transcription factor Thpok, a zinc finger protein which is required for CD4 T-cell lineage differentiation. PMID: 19696430

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Involvement in disease
Defects in Zbtb7b are the cause of helper deficient disease (HD) or helpless disease. HD and helpless mice are distinguished by the virtual absence of peripheral T-cells of the CD4(+)CD8(-) major histocompatibility complex (MHC) class II-restricted T-helper subset due to a specific block in thymic development. The developmental defect is selective for CD4(+)CD8(-) cells; the maturation of CD4(-)CD8(+) and gamma delta T-cells is normal indicating that lineage commitment is specifically perturbed without affecting positive selection. In helpless disease, NKT cells are hyperproliferative, most lack CD4 and instead express CD8. The majority of NKT cells in the thymus produce IL17 with high frequency while very few produce IFNG or other cytokines (PubMed:23105140).
Subcellular Location
Nucleus.
Tissue Specificity
Widely expressed, with a higher level in skin. Expressed in thymus. Restricted to CD4 cells (mature single positive CD4(+) and intermediate CD4(+)CD8(+) cells). Expressed in the luminal epithelial cells in the mammary glands where is up-regulated at late
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