|The CEP290 cep290 (Catalog #MBS1273363) is a cDNA Clone and is intended for research purposes only. The product is available for immediate purchase.
The CEP290 cep290 product has the following accession number(s) (GI #14250412) (NCBI Accession #BC008641). Researchers may be interested in using Bioinformatics databases such as those available at The National Center for Biotechnology Information (NCBI) website for more information about accession numbers and the proteins they represent. Even researchers unfamiliar with bioinformatics databases will find the NCBI databases to be quite user friendly and useful. The amino acid sequence is listed below:
atggccattt tcaagattgc agctctccaa aaagttgtag ataatagtgt ttctttgtct gaactagaac tggctaataa acagtacaat gaactgactg ctaagtacag ggacatcttg caaaaagata atatgcttgt tcaaagaaca agtaacttgg aacacctgga gtgtgaaaac atctccttaa aagaacaagt ggagtctata aataaagaac tggagattac caaggaaaaa cttcacacta ttgaacaagc ctgggaacag gaaactaaat taggtaatga atctagcatg gataaggcaa agaaatcaat aaccaacagt gacattgttt ccatttcaaa aaaaataact atgctggaaa tgaaggaatt aaatgaaagg cagcgggctg aacattgtca aaaaatgtat gaacacttac ggacttcgtt aaagcaaatg gaggaacgta attttgaatt ggaaaccaaa tttgctgagg tttga.
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Vector: pENTR223.1. Clone Sequence Report: Provided with product shipment. The following patways have been known to be associated with this gene. Blood, Bone, Brain, Connective Tissue, Embryonic Tissue, Eye, Kidney, Liver, Muscle, Vascular tissues are correlated with this protein. Bardet-Biedl Syndrome, Congenital Abnormalities, Fibrosis, Kidney Diseases, Leber Congenital Amaurosis 10, Liver Diseases, Neoplasms, Nerve Degeneration, Nervous System Diseases, Retinal Degeneration are some of the diseases may be linked to CEP290 cDNA Clone.