FANCF anticorps (AA 21-60)

N° du produit ABIN731633

L’anticorps anti-FANCF Polyclonal Lapin est utilisé pour la détection de FANCF dans des échantillons de Humain. Il a été validé pour IHC (p), IF (cc), IF (p) et IHC (fro).

Aperçu rapide pour FANCF anticorps (AA 21-60) (ABIN731633)

Antigène: FANCF (Fanconi Anemia, Complementation Group F (FANCF))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FANCF est non-conjugé

Application: Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-FANCF anticorps

Épitope: AA 21-60

Fonction: FANCF Polyclonal Antibody

Réactivité croisée: Souris

Homologie: Human,Rat,Cow

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FANCF

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Stockage commentaire: Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur FANCF

Antigène: FANCF (Fanconi Anemia, Complementation Group F (FANCF))

Autre désignation: FANCF

Sujet:

Synonyms: Fanconi Anemia Complementation Group F, FACF, FAF, Fanconi anemia group F protein, MGC126856, Protein FACF, FANCF_HUMAN.

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 F. [provided by RefSeq].

ID gène: 2188

Pathways: Réparation de l'ADN