LMAN1 anticorps

N° du produit ABIN2724841

L’anticorps Souris Monoclonal anti-LMAN1 a été validé pour WB, IHC, IF et FACS. Il convient pour détecter LMAN1 dans des échantillons de Humain, Rat, Chien et Singe.

Aperçu rapide pour LMAN1 anticorps (ABIN2724841)

Antigène: LMAN1 (Lectin, Mannose-Binding, 1 (LMAN1))

Reactivité: Humain, Rat, Chien, Singe

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp LMAN1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (FACS)

Clone: 1A8

Détail du produit anti-LMAN1 anticorps

Attributs du produit: Homo sapiens lectin, mannose-binding, 1 (LMAN1)

Purification: Purified from mouse ascites fluids by affinity chromatography

Immunogène: Full length human recombinant protein of human LMAN1 (NP_005561) produced in HEK293T cell.

Isotype: IgG1

Information d'application

Indications d'application: WB 1:200~500, IHC 1:150, IF 1:100, FLOW 1:100

Commentaires:

The concentration of the product may vary between diferrent lots.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5-1.0 mg/mL

Buffer: PBS (PH 7.3) containing 1 % BSA, 50 % glycerol 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

Détails sur LMAN1

Antigène: LMAN1 (Lectin, Mannose-Binding, 1 (LMAN1))

Autre désignation: LMAN1

Sujet: The protein encoded by this gene is a type I integral membrane protein localized in the intermediate region between the endoplasmic reticulum and the Golgi, presumably recycling between the two compartments. The protein is a mannose-specific lectin and is a member of a novel family of plant lectin homologs in the secretory pathway of animal cells. Mutations in the gene are associated with a coagulation defect. Using positional cloning, the gene was identified as the disease gene leading to combined factor V-factor VIII deficiency, a rare, autosomal recessive disorder in which both coagulation factors V and VIII are diminished.

Poids moléculaire: 54.2 kDa

ID gène: 3998

NCBI Accession: NM_005570

HGNC: 3998