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General Transcription Factor III (GTF2I) Peptide

GTF2I 适用: 人 宿主: 合成 BP, WB, IHC
产品编号 ABIN977774
发货至: 中国
  • 抗原 See all GTF2I products
    GTF2I (General Transcription Factor III (GTF2I))
    宿主
    资源
    • 1
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    产品特性
    This is a synthetic peptide designed for use in combination with anti-GTF2I antibody (Catalog #: ARP31910_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    纯化方法
    Purified
  • 应用备注
    Each Investigator should determine their own optimal working dilution for specific applications.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    浓度
    1 mg/mL
    缓冲液
    Final peptide concentration is 1 mg/mL in PBS.
    注意事项
    Avoid repeated freeze-thaw cycles.
    储存条件
    -20 °C
    储存方法
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 抗原
    GTF2I (General Transcription Factor III (GTF2I))
    别名
    BAP135 Peptide, BTKAP1 Peptide, DIWS Peptide, GTFII-I Peptide, IB291 Peptide, SPIN Peptide, TFII-I Peptide, WBS Peptide, WBSCR6 Peptide, Gtf2ird1 Peptide, 6030441I21Rik Peptide, BAP-135 Peptide, GtfII-I Peptide, Spin Peptide, bap-135 Peptide, bap135 Peptide, btkap1 Peptide, diws Peptide, gtfii-i Peptide, ib291 Peptide, spin Peptide, tfii-i Peptide, wbs Peptide, wbscr6 Peptide, gtf2i Peptide, gtf2i.L Peptide, general transcription factor IIi Peptide, general transcription factor II I Peptide, general transcription factor IIi S homeolog Peptide, GTF2I Peptide, Gtf2i Peptide, gtf2i Peptide, gtf2i.S Peptide
    背景
    GTF2I is a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23.This gene encodes a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. The exon(s) encoding 5' UTR has not been fully defined, but this gene is known to contain at least 34 exons, and its alternative splicing generates 4 transcript variants.

    Alias Symbols: WBS, DIWS, SPIN, IB291, BAP135, BTKAP1, TFII-I, WBSCR6, GTFII-I

    Protein Interaction Partner: ATF6,BTK,GTF2I,HDAC3,JAK2,MAPK3,MYC,NFKB2,PIAS2,PRKG1,PRRX1,SMAD2,SRC,SRF,STAT1,STAT3,USF1,YY1,ZBTB17,ATF6,BTK,HDAC1,HDAC2,HDAC3,HDAC3,KDM1A,MAPK3,MEPCE,MYC,NAA38,NFI1,OTUB2,PHF21A,PRKG1,PRRX1,PTP4A3,Pias2,SRF,STAT1,STAT3,STX7,SUZ12,USF1,USP7

    Protein Size: 978
    分子量
    110 kDa
    基因ID
    2969
    NCBI登录号
    NM_033000, NP_127493
    UniProt
    Q75M86
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