FANCM anticorps (AA 390-660)

N° du produit ABIN6140478

L’anticorps Lapin Polyclonal anti-FANCM a été validé pour WB et IF. Il convient pour détecter FANCM dans des échantillons de Humain.

Aperçu rapide pour FANCM anticorps (AA 390-660) (ABIN6140478)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FANCM est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF)

Détail du produit anti-FANCM anticorps

Épitope: AA 390-660

Séquence: MDGTKGMTRS KNELGRNEDF MKLYNHLECM FARTRSTSAN GISAIQQGDK NKKFVYSHPK LKKLEEVVIE HFKSWNAENT TEKKRDETRV MIFSSFRDSV QEIAEMLSQH QPIIRVMTFV GHASGKSTKG FTQKEQLEVV KQFRDGGYNT LVSTCVGEEG LDIGEVDLII CFDSQKSPIR LVQRMGRTGR KRQGRIVIIL SEGREERIYN QSQSNKRSIY KAISSNRQVL HFYQRSPRMV PDGINPKLHK MFITHGVYEP EKPSRNLQRK S

Réactivité croisée: Humain

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 390-660 of human FANCM (NP_065988.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IF,1:50 - 1:100

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

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

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur FANCM

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

Autre désignation: FANCM

Sujet: 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 M. Alternative splicing results in multiple transcript variants.,FANCM,FAAP250,KIAA1596,Epigenetics & Nuclear Signaling,DNA Damage & Repair,FANCM

Poids moléculaire: 75 kDa/229 kDa/232 kDa

ID gène: 57697

UniProt: Q8IYD8

Pathways: Réparation de l'ADN