Complement Factor H anticorps (AA 136-447) (HRP)

N° du produit ABIN7981553

Cet anticorps anti-Complement Factor H Polyclonal Lapin conjugué à HRP (ABIN7981553) détecte spécifiquement Complement Factor H dans WB, IHC et ELISA. L’anticorps est réactif avec des échantillons de Rat et Souris.

Aperçu rapide pour Complement Factor H anticorps (AA 136-447) (HRP) (ABIN7981553)

Antigène: Complement Factor H (CFH)

Reactivité: Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Complement Factor H est conjugé à/à la HRP

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA

Détail du produit anti-Complement Factor H anticorps (HRP)

Épitope: AA 136-447

Fonction: Anti-Factor H/Cfh Antibody HRP Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived mouse Factor H/Cfh recombinant protein (Position: N136-T447).

Isotype: IgG

Information d'application

Indications d'application: Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

Stock: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur Complement Factor H

Antigène: Complement Factor H (CFH)

Autre désignation: Cfh

Sujet:

Background: Factor H is a member of the regulators of complement activation family and is a complement control protein. This gene is a member of the Regulator of Complement Activation (RCA) gene cluster and encodes a protein with twenty short consensus repeat (SCR) domains. This protein is secreted into the bloodstream and has an essential role in the regulation of complement activation, restricting this innate defense mechanism to microbial infections. Mutations in this gene have been associated with hemolytic-uremic syndrome (HUS) and chronic hypocomplementemic nephropathy. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.

Gene Full Name: complement component factor h

ID gène: 12628

UniProt: P06909

Pathways: Système du Complément, Cellular Response to Molecule of Bacterial Origin