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Complement Factor I 抗体 (AA 19-300)

This anti-Complement Factor I antibody is a 兔 多克隆 antibody detecting Complement Factor I in WB. Suitable for 人.
产品编号 ABIN6138461
发货至: 中国

Quick Overview for Complement Factor I 抗体 (AA 19-300) (ABIN6138461)

抗原

See all Complement Factor I (CFI) 抗体
Complement Factor I (CFI)

适用

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宿主

  • 36
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克隆类型

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  • 1
多克隆

标记

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This Complement Factor I antibody is un-conjugated

应用范围

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Western Blotting (WB)
  • 抗原表位

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    AA 19-300

    序列

    KVTYTSQEDL VEKKCLAKKY THLSCDKVFC QPWQRCIEGT CVCKLPYQCP KNGTAVCATN RRSFPTYCQQ KSLECLHPGT KFLNNGTCTA EGKFSVSLKH GNTDSEGIVE VKLVDQDKTM FICKSSWSMR EANVACLDLG FQQGADTQRR FKLSDLSINS TECLHVHCRG LETSLAECTF TKRRTMGYQD FADVVCYTQK ADSPMDDFFQ CVNGKYISQM KACDGINDCG DQSDELCCKA CQGKGFHCKS GVCIPSQYQC NGEVDCITGE DEVGCAGFAS VA

    交叉反应

    人, 小鼠

    产品特性

    Polyclonal Antibodies

    纯化方法

    Affinity purification

    免疫原

    Recombinant fusion protein containing a sequence corresponding to amino acids 19-300 of human CFI (NP_000195.2).

    亚型

    IgG
  • 应用备注

    WB,1:500 - 1:2000

    说明

    HIGH QUALITY

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    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

    Complement Factor I (CFI)

    别名

    CFI

    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 uremic syndrome, a disease characterized by acute renal failure, microangiopathic hemolytic anemia and thrombocytopenia. Primary glomerulonephritis with immune deposits and age-related macular degeneration are other conditions associated with mutations of this gene.,CFI,AHUS3,ARMD13,C3BINA,C3b-INA,FI,IF,KAF,Immunology & Inflammation,Cell Intrinsic Innate Immunity Signaling Pathway,CFI

    分子量

    65 kDa

    基因ID

    3426

    UniProt

    P05156

    途径

    Complement System
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