FANCE anticorps (AA 431-536) (Cy5)

N° du produit ABIN1704564

Cet anticorps anti-FANCE est un anticorps Lapin Polyclonal détectant FANCE dans WB, IF (cc) et IF (p). Adapté pour Humain.

Aperçu rapide pour FANCE anticorps (AA 431-536) (Cy5) (ABIN1704564)

Antigène: FANCE (Fanconi Anemia, Complementation Group E (FANCE))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FANCE est conjugé à/à la Cy5

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Détail du produit anti-FANCE anticorps (Cy5)

Épitope: AA 431-536

Homologie: Human,Mouse,Rat,Dog

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FANCE

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

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: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur FANCE

Antigène: FANCE (Fanconi Anemia, Complementation Group E (FANCE))

Autre désignation: FANCE

Sujet:

Synonyms: 2810451D06Rik, AI415634, AW209126, FACE, FAE, FANCE, FANCE_HUMAN, Fanconi anemia complementation group E, Fanconi anemia group E protein, Protein FACE, RGD1561045.

Background: 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). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity, they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group E. [provided by RefSeq, Jul 2008].

ID gène: 2178

Pathways: Réparation de l'ADN