CFP anticorps (AA 197-223)

N° du produit ABIN653898

Cet anticorps anti-CFP est un anticorps Lapin Polyclonal détectant CFP dans WB et FACS. Adapté pour Humain.

Aperçu rapide pour CFP anticorps (AA 197-223) (ABIN653898)

Antigène: CFP (Complement Factor P (CFP))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CFP est non-conjugé

Application: Western Blotting (WB), Flow Cytometry (FACS)

Clone: RB22181

Détail du produit anti-CFP anticorps

Épitope: AA 197-223

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

Immunogène: This CFP antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 197-223 amino acids from the Central region of human CFP.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:500. FC: 1:10~50

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 CFP

Antigène: CFP (Complement Factor P (CFP))

Autre désignation: CFP

Sujet: This gene encodes a plasma glycoprotein that positively regulates the alternative complement pathway of the innate immune system. This protein binds to many microbial surfaces and apoptotic cells and stabilizes the C3- and C5-convertase enzyme complexes in a feedback loop that ultimately leads to formation of the membrane attack complex and lysis of the target cell. Mutations in this gene result in two forms of properdin deficiency, which results in high susceptibility to meningococcal infections.

Poids moléculaire: 51276

ID gène: 5199

NCBI Accession: NP_001138724, NP_002612

UniProt: P27918

Pathways: Système du Complément