|The NIPBL nipbl (Catalog #MBS1277549) is a cDNA Clone and is intended for research purposes only. The product is available for immediate purchase.
The NIPBL nipbl product has the following accession number(s) (GI #21708154) (NCBI Accession #BC033847). 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:
atgaaatgtt tgccagaaaa ttcagctcct ttaatcgaat ttgcaaatgt gtcccagggt attttattac ttctcatgtt aaaacaacat ttgaagaatc tttgtggatt ttctgatagt aaaattcaga agtactctcc atctgaatct gcaaaagtat atgataaagc gataaaccga aaaacaggag ttcattttca tccaaaacaa acactggact tcctgcggag tgacatggct aattccaaaa tcacagaaga ggtgaaaagg agtatagtaa aacagtatct agatttcaaa cttctcatgg aacatctgga ccctgatgaa gaagaagaag aaggggaggt ttcagctagc acaaatgctc ggaacaaagc aattacctca ctgcttggag gaggcagccc taaaaataat acagcagcag agacagaaga tgatgaaagt gatggggagg atagaggagg aggcacttca ggggtgaggc ggaggaggag tcaacgtatt tcgcagcgta ttacgtaa.
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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, Connective Tissue, Embryonic Tissue, Esophagus, Eye, Heart, Kidney, Mouth, Muscle tissues are correlated with this protein. Abnormalities, Multiple, Bone Diseases, Developmental, Congenital Abnormalities, Craniofacial Abnormalities, De Lange Syndrome, Death, Disease Models, Animal, Heart Defects, Congenital, Neoplasms, Nervous System Diseases are some of the diseases may be linked to NIPBL cDNA Clone.