CLDND1 anticorps

N° du produit ABIN7239830

Détail du produit anti-CLDND1 anticorps

Antigène: CLDND1 (Claudin Domain Containing 1 (CLDND1))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CLDND1 est non-conjugé

Application: ELISA, Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant protein of human CLDND1

Isotype: IgG

Information d'application

Indications d'application: IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.2 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

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 CLDND1

Antigène: CLDND1 (Claudin Domain Containing 1 (CLDND1))

Autre désignation: CLDND1 (CLDND1 Produits)

Synonymes: anticorps MGC53751, anticorps LOC100217896, anticorps 1110019C08Rik, anticorps AA407103, anticorps AI849195, anticorps AW489850, anticorps Cldnd1, anticorps C3orf4, anticorps GENX-3745, anticorps claudin domain containing 1 L homeolog, anticorps claudin domain containing 1, anticorps cldnd1.L, anticorps cldnd1, anticorps CLDND1, anticorps Cldnd1

Sujet: CLDND1 (claudin domain containing 1), also known as C3orf4 or HSPC174, is a 253 amino acid multi-pass membrane protein that is expressed at high levels in adult brain and at lower levels in adult heart. Existing as two alternatively spliced isoforms, CLDND1 is encoded by a gene that maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

UniProt: Q9NY35