CLDND1 anticorps
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- Antigène Voir toutes CLDND1 Anticorps
- CLDND1 (Claudin Domain Containing 1 (CLDND1))
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp CLDND1 est non-conjugé
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Application
- ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
- Réactivité croisée
- Humain, Souris
- Purification
- Antigen affinity purification
- Immunogène
- Fusion protein of Human CLDND1
- Isotype
- IgG
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- Indications d'application
- ELISA:1:2000-1:5000, WB:1:200-1:1000, IHC:1:50-1:200,
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
- 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,-80 °C
- Stockage commentaire
- Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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- 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
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Background: 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.
Aliases: CLDND1 antibody, C3orf4 antibody, HSPC174 antibody, PSEC0054 antibody, UNQ2511/PRO6000Claudin domain-containing protein 1 antibody, Membrane protein GENX-3745 antibody
- UniProt
- Q9NY35
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