Recombinant FANCM anticorps

N° du produit ABIN7938129

Cet anticorps anti-FANCM Monoclonal Lapin (Clone 230233G5) (ABIN7938129) détecte spécifiquement FANCM dans IP. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour Recombinant FANCM anticorps (ABIN7938129)

Antigène: FANCM (Fanconi Anemia Complementation Group M (FANCM))

Type d'anticorp: Recombinant Antibody

Reactivité: Humain

Hôte: Lapin

Clonalité: Monoclonal

Conjugué: Cet anticorp FANCM est non-conjugé

Application: Immunoprecipitation (IP)

Clone: 230233G5

Détail du produit anti-FANCM anticorps

Fonction: FANCM antibody (rAb), 100 μg (Clone 230233G5)

Purification: Protein A Chromatography

Immunogène: This antibody was raised against the FANCM fusion protein.

Isotype: IgG

Information d'application

Indications d'application: IP: 4 μg per IP

Restrictions: For Research Use only

Stockage

Buffer: Purified IgG in PBS, pH 7.3, with 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.

Conseil sur la manipulation: Avoid repeated freeze/thaw cycles by aliquoting items into single-use fractions,Keep all reagents on ice when not in storage

Stock: -20 °C

Stockage commentaire: Some products may be shipped at room temperature. This will not affect their stability or performance. Avoid repeated freeze/thaw cycles by aliquoting items into single-use fractions for storage at -20°C for up to 2 years. Keep all reagents on ice when not in storage.

Date de péremption: 24 months

Détails sur FANCM

Antigène: FANCM (Fanconi Anemia Complementation Group M (FANCM))

Autre désignation: FANCM

Sujet:

Background_Plain: The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair.

Aliases: Fanconi anemia complementation group M, FAAP250

Poids moléculaire: 180-200 kDa

Pathways: Réparation de l'ADN