Recombinant Human Transcription initiation factor TFIID subunit 1 (TAF1), partial

Code CSB-YP023076HU
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Source Yeast
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Code CSB-EP023076HU
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Source E.coli
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Code CSB-EP023076HU-B
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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-BP023076HU
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Source Baculovirus
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Code CSB-MP023076HU
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Source Mammalian cell
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Product Details

Purity
>85% (SDS-PAGE)
Target Names
TAF1
Uniprot No.
Alternative Names
BA2R; CCG1; CCGS; Cell cycle G1 phase defect; Cell cycle gene 1 protein; Complementation of cell cycle block G1 to S; DYT3; N TAF1; NSCL2; OF; p250; TAF 1; TAF(II)250; TAF1; TAF1 RNA polymerase II TATA box binding protein (TBP) associated factor 250kDa; TAF1_HUMAN; TAF2A; TAFII-250; TAFII250; TATA box binding protein (TBP) associated factor RNA polymerase II A 250kD; TBP associated factor 250 kDa; TBP-associated factor 250 kDa; Transcription factor TFIID p250 polypeptide; Transcription initiation factor TFIID 250 kDa subunit; Transcription initiation factor TFIID subunit 1; XDP
Species
Homo sapiens (Human)
Protein Length
Partial
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.

Customer Reviews and Q&A

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Target Background

Function
Largest component and core scaffold of the TFIID basal transcription factor complex. Contains novel N- and C-terminal Ser/Thr kinase domains which can autophosphorylate or transphosphorylate other transcription factors. Phosphorylates TP53 on 'Thr-55' which leads to MDM2-mediated degradation of TP53. Phosphorylates GTF2A1 and GTF2F1 on Ser residues. Possesses DNA-binding activity. Essential for progression of the G1 phase of the cell cycle. Exhibits histone acetyltransferase activity towards histones H3 and H4.
Gene References into Functions
  1. Our findings highlight the regulatory networks among TFs, lncRNAs, miRNAs, and mRNAs in hepatocellular carcinoma (HCC). Several key molecules, such as hsa-miR-195, lncRNA MALAT1 and TFs TAF1 and HNF4alpha, may contribute to the progression of HCC. PMID: 30249878
  2. These data directly link sequence variation within the XDP-specific SVA sequence to phenotypic variability in clinical disease manifestation and provide insight into potential mechanisms by which this intronic retroelement may induce transcriptional interference in TAF1 expression. PMID: 29229810
  3. present a case study where a combination of experimental techniques and computational simulations was used to comprehensively characterize the binding and structure-affinity relationships for a series of Bromosporine-based bivalent bromodomain ligands with a bivalent protein, Transcription Initiation Factor TFIID subunit 1 (TAF1). PMID: 29558110
  4. The results converge on TAF1 dysfunction in peripheral models of X-linked dystonia-parkinsonism, and provide evidence of altered expression of a canonical gene in this disease. Furthermore, this study illustrates a link between the previously described genetic alterations and TAF1 dysfunction at the transcriptome level. PMID: 26879577
  5. TAF1 and TAF1L genes harbored not only somatic mutations but also mutational ITH. PMID: 27571988
  6. N-TAF1 expression is impaired in X-linked dystonia-parkinsonism. PMID: 26769797
  7. The bromodomains of BRD9, CECR2, and the second bromodomain of TAF1 recognize the longer butyryl mark on histones. In addition, the TAF1 second bromodomain is capable of binding crotonyl marks. PMID: 26365797
  8. TAF1 variants are associated with dysmorphic features, intellectual disability, and neurological manifestations. PMID: 26637982
  9. are necessary and sufficient to overcome the barrier of species specificity for human rDNA transcription in mouse cells PMID: 24928901
  10. TAF1 winged helix domain has intrinsic DNA-binding activity, which depends on characteristic residues that are commonly used by winged helix fold proteins for interacting with DNA. PMID: 25412659
  11. the surface of the TAF1-TAF7 complex contains two prominent conserved surface pockets, one of which binds selectively to an inhibitory trimethylated histone H3 PMID: 24927529
  12. This study demonistrated that frequencies of polymorphic genotype and allele of TAF1 gene were not different in patients than in control group and that they were not significant for cerebral venous thrombosis. PMID: 23264082
  13. As cellular ATP levels recover, TAF1 is able to phosphorylate p53 on Thr55, which leads to dissociation of p53 from the p21 promoter. PMID: 24289924
  14. Lower efficiency of microRNA synthesis directed by TATA box or NF-kappaappaB is a consequence of frequent transcription initiations that lead to RNA polymerase II crowding at pause sites and premature termination. PMID: 23831825
  15. Although d3-d4 also affect genes potentially related to neurodegenerative processes, their physiologic role as splice variants of TAF1 awaits further exploration PMID: 23184149
  16. analysis of phosphorylation-dependent regulation of cyclin D1 and cyclin A gene transcription by TFIID subunits TAF1 and TAF7 PMID: 22711989
  17. In the Brazilian population, genetic variations in both uPA and TAFI were not relevant to endometriosis and/or infertility. PMID: 21819230
  18. TAF7, until now considered only a TFIID component and regulator of TAF1-dependent transcription, also regulates TAF1-independent transcription PMID: 20937824
  19. 285 patients with autosomal -dominant ataxia were examined, and abnormal or borderline expansions of CAG/CAA within TBP were found. PMID: 20587494
  20. Results indicate that increased TAF1 expression is associated with progression of human prostate cancers to the lethal castration-resistant state. PMID: 20181722
  21. polymorphism of TAF1 gene does not influence the risk of myocardial infarction. PMID: 11871391
  22. Evidence that TAF-TATA box-binding protein interactions are required for activated transcription in mammalian cells. PMID: 11909971
  23. TAF1 may be involved in the coordinate expression of Pol I- and Pol II-transcribed genes required for protein biosynthesis and cell cycle progression. PMID: 12498690
  24. TAFI polymorphisms investigated exerted no thrombogenic influence in pediatric oncology patients. PMID: 14719174
  25. TAF1 induces G1 progression in a p53-dependent manner. It interacts with and phosphorylates p53 at Thr-55 in vivo. PMID: 15053879
  26. hsTAF1 derepression of transcription requires the leucine zipper domain of c-Jun to bind to the N terminus of hsTAF1 PMID: 15087451
  27. TAF1-dependent histone acetylation facilitates transcription factor binding to the Sp1 sites, thereby activating cyclin D1 transcription and ultimately G(1)-to-S-phase progression PMID: 15870300
  28. DYT3 is the gene responsible for X-linked recessive dystonia-parkinsonism. PMID: 16366515
  29. linkage disequilibrium observed in an African population enabled us to identify the 1583T>A SNP located in 3'UTR. PMID: 16705091
  30. Downregulates E3 ubiquitin ligase Mdm2 auto-ubiquitylation, leading to Mdm2 stabilization, and promotes p53-Mdm2 association. PMID: 17237821
  31. Reduced neuron-specific expression of the TAF1 gene is associated with X-linked dystonia-parkinsonism PMID: 17273961
  32. possible sites in hUBF HMG box 5 that may interact with the first bromodomain of TAF1 were proposed PMID: 17505112
  33. Thirty-eight exons code for TAF1. Five downstream exons of yet unknown function can either form transcripts with TAF1 exons or be transcribed independently. Splice variants can include d plus at least 12 TAF1 exons. PMID: 17952504
  34. CK2 is tightly associated with TAFII250 and is the principal activity responsible for TAFII250-mediated phosphorylation of Mdm2. PMID: 18548200
  35. interacts with human papillomavirus 16 E2 protein. PMID: 18580066

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Involvement in disease
Dystonia 3, torsion, X-linked (DYT3); Mental retardation, X-linked, syndromic, 33 (MRXS33)
Subcellular Location
Nucleus.
Protein Families
TAF1 family
Database Links

HGNC: 11535

OMIM: 300966

KEGG: hsa:6872

STRING: 9606.ENSP00000276072

UniGene: Hs.158560

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