IGHMBP2 anticorps

N° du produit ABIN7231406

Cet anticorps anti-IGHMBP2 Polyclonal Lapin (ABIN7231406) détecte spécifiquement IGHMBP2 dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour IGHMBP2 anticorps (ABIN7231406)

Antigène: IGHMBP2 (Immunoglobulin mu Binding Protein 2 (IGHMBP2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp IGHMBP2 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-IGHMBP2 anticorps

Fonction: Rabbit Anti-SMBP2 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of SMBP2 protein

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

Immunogène: Synthesized peptide derived from part region of human SMBP2 protein

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur IGHMBP2

Antigène: IGHMBP2 (Immunoglobulin mu Binding Protein 2 (IGHMBP2))

Autre désignation: SMBP2

Sujet: DNA-binding protein SMUBP-2, ATP-dependent helicase IGHMBP2, Glial factor 1, GF-1, Immunoglobulin mu-binding protein 2IGHMBP2 (Immunoglobulin Mu Binding Protein 2) is a Protein Coding gene. Diseases associated with IGHMBP2 include Neuronopathy, Distal Hereditary Motor, Type Vi and Charcot-Marie-Tooth Disease, Axonal, Type 2S. IGHMBP2 encodes a helicase superfamily member that binds a specific DNA sequence from the immunoglobulin mu chain switch region. Mutations in this gene lead to spinal muscle atrophy with respiratory distress type 1.

Poids moléculaire: 109kD

ID gène: 3508

UniProt: P38935