Complement Factor H anticorps (AA 751-780)

N° du produit ABIN7876733

Cet anticorps Lapin Polyclonal détecte spécifiquement Complement Factor H dans WB, IF et IHC (p). Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour Complement Factor H anticorps (AA 751-780) (ABIN7876733)

Antigène: Complement Factor H (CFH)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Complement Factor H est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-Complement Factor H anticorps

Épitope: AA 751-780

Fonction: Complement factor H Antibody / CFH

Purification: Antigen affinity purified

Immunogène: A portion of amino acids 751-780 from the human protein was used as the immunogen for the Complement factor H antibody.

Isotype: IgG

Information d'application

Indications d'application: The stated application concentrations are suggested starting points. Titration of the Complement factor H antibody may be required due to differences in protocols and secondary/substrate sensitivity.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: In 1X PBS, pH 7.4, with 0.09 % 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: Aliquot the Complement factor H antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Détails sur Complement Factor H

Antigène: Complement Factor H (CFH)

Autre désignation: Complement factor H

Sujet: This gene is a member of the Regulator of Complement Activation (RCA) gene cluster and encodes a protein with twenty short concensus 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.

UniProt: P08603

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