Complement Factor H anticorps (AA 751-780)

N° du produit ABIN654896

L’anticorps Lapin Polyclonal anti-Complement Factor H a été validé pour WB, IF et IHC (p). Il convient pour détecter Complement Factor H dans des échantillons de Humain.

Aperçu rapide pour Complement Factor H anticorps (AA 751-780) (ABIN654896)

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))

Clone: RB18698

Détail du produit anti-Complement Factor H anticorps

Épitope: AA 751-780

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This CFH antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 751-780 amino acids of human CFH.

Isotype: IgG

Information d'application

Indications d'application: IF: 1:25. IF: 1:25. WB: 1:2000. WB: 1:2000. IHC-P: 1:50~100

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Stockage commentaire: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Détails sur Complement Factor H

Antigène: Complement Factor H (CFH)

Autre désignation: CFH

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.

Poids moléculaire: 139096

ID gène: 3075

NCBI Accession: NP_000177

UniProt: P08603

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