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Rabbit Anti-GLT8D1/FITC Conjugated antibody
background:
GLT8D1 is a 371 amino acid single-pass type II transmembrane protein that is expressed by a gene residing on human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding 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. There are two isoforms of GLT8D1 that are produced as a result of alternative splicing events.
Subcellular Location:
Membrane; Single pass type II membrane protein
Similarity:
Belongs to the glycosyltransferase 8 family.
Database links:
Entrez Gene: 55830 Human
Entrez Gene: 76485 Mouse
Entrez Gene: 306253 Rat
SwissProt: Q68CQ7 Human
SwissProt: Q6NSU3 Mouse
SwissProt: Q6AYF6 Rat
Unigene: 297304 Human
Unigene: 8766 Mouse
Unigene: 91636 Rat
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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