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Complement Factor I 抗体 (N-Term)

The 兔 多克隆 anti-Complement Factor I antibody is suitable to detect Complement Factor I in samples from 人. It has been validated for WB.
产品编号 ABIN2789418
发货至: 中国
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中国
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for Complement Factor I 抗体 (N-Term) (ABIN2789418)

抗原

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

适用

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人

宿主

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兔

克隆类型

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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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    N-Term

    原理

    CFI Antibody - N-terminal region

    序列

    WSMREANVAC LDLGFQQGAD TQRRFKLSDL SINSTECLHV HCRGLETSLA

    预测反应

    Human: 100%

    产品特性

    This is a rabbit polyclonal antibody against CFI. It was validated on Western Blot.

    纯化方法

    Affinity Purified
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    说明

    We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP63227-100UG

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.5 mg/mL

    缓冲液

    Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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.

    注意事项

    prevent freeze-thaw cycles

    储存条件

    4 °C,-20 °C

    储存方法

    For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
  • 抗原

    Complement Factor I (CFI)

    别名

    CFI

    背景

    Background Information: 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.

    Gene Name: Complement factor I

    Alternative Symbols: FI, IF, KAF, AHUS3, ARMD13, C3BINA, C3b-INA

    Protein Name: Complement factor I

    分子量

    64kDa

    基因ID

    3426

    NCBI登录号

    NP_000195

    UniProt

    P05156

    途径

    Complement System
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