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Surfeit 1 (SURF1) Peptide

SURF1 适用: 哺乳动物 宿主: 合成 BP, WB, IHC
产品编号 ABIN938801
发货至: 中国
  • 抗原 See all SURF1 products
    SURF1 (Surfeit 1 (SURF1))
    蛋白类型
    Synthetic
    宿主
    哺乳动物
    资源
    • 2
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    序列
    GLRAAGLGRA PASAAWRSVL RVSPRPGVAW RPSRCGSSAA EASATKAEDD
    产品特性
    A synthetic peptide for use as a blocking control in assays to test for specificity of SURF1 antibody,
    Alternative Names: SURF1 control peptide, SURF1 antibody Blocking Peptide, Anti-SURF1 Blocking Peptide, surfeit 1 Blocking Peptide, SURF1, SURF-1, SURF 1, SURF-1 Blocking Peptide, SURF 1 Blocking Peptide
  • 应用备注
    Optimal conditions should be determined by the investigator
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
    缓冲液
    PBS
    注意事项
    Avoid repeated freeze/thaw cycles.
    储存条件
    -20 °C
    储存方法
    Store at -20 °C long term.
  • 抗原
    SURF1 (Surfeit 1 (SURF1))
    别名
    BcDNA:GH23574 Peptide, CG9943 Peptide, Dmel\\CG9943 Peptide, GB14201 Peptide, SURF1 Peptide, im:6898613 Peptide, zgc:158646 Peptide, Ab1-205 Peptide, SURF-1 Peptide, 0610010F23Rik Peptide, Surf-1 Peptide, SURFEIT 1 Peptide, Surfeit 1 Peptide, surfeit locus protein 1 Peptide, SURF1, cytochrome c oxidase assembly factor Peptide, surfeit 1 Peptide, surfeit gene 1 Peptide, Surfeit locus 1 cytochrome c oxidase biogenesis protein Peptide, Surf1 Peptide, LOC413781 Peptide, SURF1 Peptide, surf1 Peptide
    背景
    This gene encodes a protein localized to the inner mitochondrial membrane and thought to be involved in the biogenesis of the cytochrome c oxidase complex. The protein is a member of the SURF1 family, which includes the related yeast protein SHY1 and rickettsial protein RP733. The gene is located in the surfeit gene cluster, a group of very tightly linked genes that do not share sequence similarity, where it shares a bidirectional promoter with SURF2 on the opposite strand. Defects in this gene are a cause of Leigh syndrome, a severe neurological disorder that is commonly associated with systemic cytochrome c oxidase deficiency.
    分子量
    33 kDa
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