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200μL $ 399.00
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For research use only.

Verified Samples Verified Samples in IHC: Human colon cancer, Human brain
Dilution IHC 1:50-1:200
Isotype Rabbit IgG
Host Rabbit
Reactivity Human,  Mouse
Applications IHC
Clonality Polyclonal
Immunogen Recombinant protein of human CLDND1
Abbre CLDND1
Synonyms C3orf4,  Chromosome 3 open reading frame 4,  Claudin domain containing 1,  Claudin domain containing 1 protein,  GENX 3745,  Membrane protein GENX3745,  MGC111162,  MGC3316,  MGC9861,  OTTHUMP00000,  OTTHUMP00000217407,  OTTHUMP00000217408,  OTTHUMP00000217423,  OTTHUMP00000217424,  OTTHUMP00000217562,  OTTHUMP00000217563,  OTTHUMP00000217584,  OTTHUMP00000217585,  OTTHUMP00000217586,  OTTHUMP00000217587,  OTTHUMP00000217609,  OTTHUMP00000217610,  OTTHUMP00000217611,  OTTHUMP00000217622,  OTTHUMP00000217623,  OTTHUMP00000217625,  OTTHUMP00000217627,  OTTHUMP00000217628,  OTTHUMP00000217638抗体
Swissprot
Cellular Localization Membrane, Multi pass membrane protein.
Concentration 0.2 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Purification Method Affinity purification
Research Areas Cell Biology,  Neuroscience
Conjugation Unconjugated
Storage Store at -20℃ Valid for 12 months. Avoid freeze/thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
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.
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