Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Complement Factor I antibody (AA 19-220)

The Rabbit Polyclonal anti-Complement Factor I antibody is suitable to detect Complement Factor I in samples from Human and Rat. It has been validated for WB, IHC, ICC and FACS.
Catalog No. ABIN7981579
$370.00
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 4 to 7 Business Days

Quick Overview for Complement Factor I antibody (AA 19-220) (ABIN7981579)

Target

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

Reactivity

  • 63
  • 13
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Rat

Host

  • 45
  • 19
Rabbit

Clonality

  • 47
  • 16
  • 1
Polyclonal

Conjugate

  • 35
  • 6
  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Complement Factor I antibody is un-conjugated

Application

  • 36
  • 21
  • 17
  • 17
  • 11
  • 8
  • 8
  • 7
  • 5
  • 5
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunocytochemistry (ICC), Flow Cytometry (FACS)

Grade

Carrier-free
  • Binding Specificity

    • 11
    • 5
    • 4
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 19-220

    Purpose

    Anti-Factor I/CFI Antibody

    Specificity

    No cross reactivity with other proteins.

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins

    Predicted Reactivity

    coli-derived human Factor I recombinant protein (Position: K19-D220). Human Factor I shares 70.7%,71.2% amino acid (aa) sequence identity with mouse,rat Factor I,respectively.

    Characteristics

    Anti-Factor I/CFI Antibody. Tested in Flow Cytometry, IHC, ICC, WB applications. This antibody reacts with Human, Rat.

    Purification

    Immunogen affinity purified.

    Immunogen

    E. coli-derived human Factor I recombinant protein (Position: K19-D220). Human Factor I shares 70.7% and 71.2% amino acid (aa) sequence identity with mouse and rat Factor I, respectively.

    Isotype

    IgG
  • Application Notes

    Western blot, 0.1-0.5 μg/mL, Human, RatImmunohistochemistry (Frozen Section), 0.5-1 μg/mL, Human Immunocytochemistry, 0.5-1 μg/mL, Human Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains antibody formulated with stabilizing components, 0.9 mg NaCl, 0.2 mg Na2HPO4, and 0.05 mg Sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.

    Expiry Date

    12 months
  • Target

    Complement Factor I (CFI)

    Alternative Name

    CFI

    Background

    Background: Complement factor I, also known as C3b/C4b inactivator, is a protein that in humans is encoded by the CFI gene. 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.

    Gene Full Name: complement factor I

    Molecular Weight

    75 kDa, 45 kDa

    Gene ID

    3426

    UniProt

    P05156

    Pathways

    Complement System
You are here:
Chat with us!