Factor I anticorps (AA 410-490)

N° du produit ABIN7221664

L’anticorps Lapin Polyclonal anti-Factor I a été validé pour WB et ELISA. Il convient pour détecter Factor I dans des échantillons de Humain.

Aperçu rapide pour Factor I anticorps (AA 410-490) (ABIN7221664)

Antigène: Factor I

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Factor I est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-Factor I anticorps

Épitope: AA 410-490

Fonction: Factor I Polyclonal Antibody

Specificité: Factor I Polyclonal Antibody detects endogenous levels of Factor I protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen

Immunogène: Synthesized peptide derived from the Internal region of human Factor I at AA range: 410-490

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:10000). Not yet tested in other applications.

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Détails sur Factor I

Antigène: Factor I

Sujet: Rabbit Anti-Factor I Polyclonal Antibody,CFI, IF, Complement factor I, C3B/C4B inactivator,CFI 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.,Complement factor I

Poids moléculaire: observerd band 66kDa

ID gène: 3426

UniProt: P05156