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SOX14 抗体

SOX14 适用: 人, 小鼠, 大鼠 IHC, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6568117
发货至: 中国
  • 抗原 See all SOX14 抗体
    SOX14 (SRY (Sex Determining Region Y)-Box 14 (SOX14))
    适用
    • 30
    • 7
    • 6
    • 5
    • 4
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    人, 小鼠, 大鼠
    宿主
    • 30
    克隆类型
    • 30
    多克隆
    标记
    • 12
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This SOX14 antibody is un-conjugated
    应用范围
    • 25
    • 13
    • 13
    • 10
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human SOX14
    亚型
    IgG
    Top Product
    Discover our top product SOX14 Primary Antibody
  • 应用备注
    IHC 1:50 - 1:200 IF 1:50 - 1:200
    限制
    仅限研究用
  • 浓度
    1 mg/mL
    缓冲液
    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    SOX14 (SRY (Sex Determining Region Y)-Box 14 (SOX14))
    别名
    SOX14 (SOX14 产品)
    别名
    SOX28 antibody, zgc:123197 antibody, SRY-box 14 antibody, SRY-box 14 S homeolog antibody, SRY box 14 antibody, SRY (sex determining region Y)-box 14 antibody, SOX14 antibody, sox14.S antibody, Sox14 antibody, sox14 antibody
    背景

    Synonyms: HMG box transcription factor SOX 14,MGC119898,MGC119899,SOX 14,SOX 28,Sox box protein 14,SOX28,SRY (sex determining region Y) box 14 ,SRY box 14,Transcription factor SOX 14

    Background: This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene are suggested to be responsible for the limb defects associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) and Mobius syndrome.

    分子量

    Observed_MW: Refer to Figures

    Calculated_MW: 26kDa

    基因ID
    8403
    UniProt
    O95416
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