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Complement Factor I (CFI) (N-Term) Peptide

CFI 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN974872
发货至: 中国
  • 抗原 See all Complement Factor I (CFI) products
    Complement Factor I (CFI)
    蛋白结构域
    N-Term
    宿主
    资源
    • 1
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB)
    序列
    WSMREANVAC LDLGFQQGAD TQRRFKLSDL SINSTECLHV HCRGLETSLA
    产品特性
    This is a synthetic peptide designed for use in combination with anti-CFI Antibody. 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
    Complement Factor I (CFI)
    别名
    cfi Peptide, MGC53615 Peptide, Cfi Peptide, factor I Peptide, IF Peptide, gb:ai721528 Peptide, ahus3 Peptide, c3b-ina Peptide, c3bc4bi Peptide, c3bina Peptide, kaf Peptide, CFI Peptide, AHUS3 Peptide, C3BINA Peptide, C3b-INA Peptide, FI Peptide, KAF Peptide, complement factor I S homeolog Peptide, complement factor I L homeolog Peptide, complement factor I Peptide, complement component factor i Peptide, cfi.S Peptide, cfi.L Peptide, CFI Peptide, cfi Peptide, Cfi Peptide
    背景
    This gene encodes a serine proteinase that is essential for regulating the complement cascade. The encoded preproprotein is cleaved to produce both heavy and light chains, which are linked by disulfide bonds to form a heterodimeric glycoprotein. This heterodimer can cleave and inactivate the complement components C4b and C3b, and it prevents the assembly of the C3 and C5 convertase enzymes. Defects in this gene cause complement factor I deficiency, an autosomal recessive disease associated with a susceptibility to pyogenic infections. Mutations in this gene have been associated with a predisposition to atypical hemolytic uraemic syndrome, a disease characterized by acute renal failure, microangiopathic hemolytic anemia and thrombocytopenia. Primary glomerulonephritis with immmune deposits is another condition associated with mutation of this gene.

    Alias Symbols: AHUS3, C3BINA, C3b-INA, FI, IF, KAF

    Protein Interaction Partner: C3,CFH,C3

    Protein Size: 583
    分子量
    64 kDa
    基因ID
    3426
    NCBI登录号
    NM_000204, NP_000195
    UniProt
    P05156
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