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Sex Determining Region Y (SRY) (Middle Region) Peptide

SRY 适用: 人, 小鼠 宿主: 合成 BP, WB
产品编号 ABIN984444
发货至: 中国
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Quick Overview for Sex Determining Region Y (SRY) (Middle Region) Peptide (ABIN984444)

抗原

SRY (Sex Determining Region Y (SRY))

宿主

人, 小鼠

资源

  • 1
合成

应用范围

Blocking Peptide (BP), Western Blotting (WB)
  • 蛋白结构域

    Middle Region

    产品特性

    This is a synthetic peptide designed for use in combination with anti-SRY antibody (Catalog #: ARP34794_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

    SRY (Sex Determining Region Y (SRY))

    背景

    SRY is an intronless gene that encodes for a transcription factor, which is a member of the high mobility group (HMG)-box family of DNA-binding proteins. This protein is the testis-determining factor(TDF), which initiates male sex determination. Mutations in this gene give rise to XY females with gonadal dysgenesis (Swyer syndrome), translocation of part of the Y chromosome containing this gene to the X chromosome causes XX male syndrome.This intronless gene encodes a transcription factor that is a member of the high mobility group (HMG)-box family of DNA-binding proteins. This protein is the testis-determining factor (TDF), which initiates male sex determination. Mutations in this gene give rise to XY females with gonadal dysgenesis (Swyer syndrome), translocation of part of the Y chromosome containing this gene to the X chromosome causes XX male syndrome. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

    Alias Symbols: TDF, TDY, SRXX1, SRXY1

    Protein Interaction Partner: ZNF208,AR,SLC9A3R2,SMAD3,ZNF208,AR

    Protein Size: 204

    分子量

    24 kDa

    基因ID

    6736

    NCBI登录号

    NM_003140, NP_003131

    UniProt

    Q05066
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