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SRY (Sex Determining Region Y)-Box 2 (SOX2) (N-Term) Peptide

SOX2 适用: 人 宿主: 合成 BP, WB, IHC
产品编号 ABIN984265
发货至: 中国

Quick Overview for SRY (Sex Determining Region Y)-Box 2 (SOX2) (N-Term) Peptide (ABIN984265)

抗原

SOX2 (SRY (Sex Determining Region Y)-Box 2 (SOX2))

宿主

资源

  • 4
合成

应用范围

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

    N-Term

    产品特性

    This is a synthetic peptide designed for use in combination with anti-SOX2 antibody (Catalog #: ARP31737_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

    SOX2 (SRY (Sex Determining Region Y)-Box 2 (SOX2))

    背景

    SOX2 is a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The protein may act as a transcriptional activator after forming a protein complex with other proteins. Mutations in this gene have been associated with bilateral anophthalmia, a severe form of structural eye malformation. This intronless gene encodes a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of this gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. Mutations in this gene have been associated with optic nerve hypoplasia and with syndromic microphthalmia, a severe form of structural eye malformation. This gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). 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: ANOP3, MCOPS3, MGC2413

    Protein Interaction Partner: NR5A1,POU2F1,POU5F1,PAX6,POU5F1

    Protein Size: 317

    分子量

    34 kDa

    基因ID

    6657

    NCBI登录号

    NM_003106, NP_003097

    UniProt

    P48431
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