CLDND1 Antikörper

Produktnummer ABIN7239830

Produktdetails anti-CLDND1 Antikörper

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

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CLDND1 Antikörper ist unkonjugiert

Applikation: ELISA, Immunohistochemistry (IHC)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human CLDND1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IHC 1:50-1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.2 mg/mL

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

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu CLDND1

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

Andere Bezeichnung: CLDND1 (CLDND1 Produkte)

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

Hintergrund: 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