MBL-C anticorps (AA 21-70)

N° du produit ABIN8122759

Cet anticorps anti-MBL-C Polyclonal Lapin (ABIN8122759) détecte spécifiquement MBL-C dans WB et IHC. L’anticorps est réactif avec des échantillons de Souris et Humain.

Aperçu rapide pour MBL-C anticorps (AA 21-70) (ABIN8122759)

Antigène: MBL-C (Mannose-Binding Lectin C)

Reactivité: Souris, Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MBL-C est non-conjugé

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

Détail du produit anti-MBL-C anticorps

Épitope: AA 21-70

Fonction: MBL-C Antibody

Specificité: The antibody detects endogenous MBL-C protein

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

Immunogène: Synthetic peptide from human protein at AA range: 21-70

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-2000,IHC 1:50-300

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Liquid in 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: Store at -20°C/1 year

Date de péremption: 12 months

Détails sur MBL-C

Antigène: MBL-C (Mannose-Binding Lectin C)

Autre désignation: MBL-C

Sujet:

Synonyms: MBL2 COLEC1 MBL

Background: This gene encodes the soluble mannose-binding lectin or mannose-binding protein found in serum. The protein encoded belongs to the collectin family and is an important element in the innate immune system. The protein recognizes mannose and N-acetylglucosamine on many microorganisms, and is capable of activating the classical complement pathway. Deficiencies of this gene have been associated with susceptibility to autoimmune and infectious diseases. [provided by RefSeq, Jul 2008],

Gene Name: MBL2 COLEC1 MBL

Protein Name: mannose-binding lectin (protein C) 2, soluble (opsonic defect)

ID gène: 4153

UniProt: P11226