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NRCD human cDNA clones

Catalog number RDB06607
Resource name NRCD human cDNA clones
Alternative name human retinal pigment epithelium cell ARPE19 cDNA clone set; ARi-S
Vector backbone pGCAP10 (Plasmid)
Gene/insert name Human cDNA
Depositor|Developer Kato, Seishi |

Distribution information

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Please visit NRCD human cDNA clones.[link] 
Terms and conditions for distribution In publishing the research results to be obtained by use of the BIOLOGICAL RESOURCE, RECIPIENT must state an acknowledgment This BIOLOGICAL RESOURCE deposited by Seishi Kato, Research Institute of National Rehabilitation Center for Persons with Disabilities, was provided by the RIKEN BRC.
In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of literature (Oshikawa, M. et al. Invest. Ophthalmol. Vis. Sci. 52 (9), 6662-6670, 2011) is requested.
When requested by the DEPOSITOR, RIKEN BRC informs the DEPOSITOR on the name of resource, RECIPIENT’s name, his/her affiliation and purpose of the use.
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提供依頼書 [Word]
手続きの概要は、「NRCD human cDNA clones[link]」をご覧ください。
提供条件 研究成果の公表にあたり、国立障害者リハビリテーションセンター研究所 加藤誠志博士から提供されたことを記載すること。
利用者は、研究成果の公表にあたって 文献 (Oshikawa, M. et al. Invest. Ophthalmol. Vis. Sci. 52 (9), 6662-6670, 2011)の引用を必要とする。


Original, user report and related articles

original Kato, S., Identification of genuine alternative splicing variants for rare or long-sized transcripts. In: DiMaggio S. and Braschipp E. eds. New Developments in Alternative Splicing Research. New York, Nova Biomedical. p.89-108, 2013.
original Oshikawa, M., Full-length transcriptome analysis of human retina-derived cell lines ARPE-19 and Y79 using the vector-capping method. Invest. Ophthalmol. Vis. Sci. 52 (9): 6662-6670 (2011). PMID 21697133. [link to RRC of NBRP]
original Oshikawa, M., Fine expression profiling of full-length transcripts using a size-unbiased cDNA library prepared with the vector-capping method. DNA Res., 15, 123-136 (2008). PMID 18487259. [link to RRC of NBRP]
original Kato, S., Vector-capping: a simple method for preparing a high-quality full-length cDNA library. DNA Res., 12, 53-62 (2005). PMID 16106752. [link to RRC of NBRP]
reference Kato, S., Construction of a human full-length cDNA bank. Gene 150 (2): 243-250 (1994). PMID 7821789.
user_report Reimann, L., Phosphoproteomics identifies dual-site phosphorylation in an extended basophilic motif regulating FILIP1-mediated degradation of filamin-C. Commun. Biol. 3 (1): 253 (2020). PMID 32444788. [link to RRC of NBRP]
user_report Kamil, M., High filamin-C expression predicts enhanced invasiveness and poor outcome in glioblastoma multiforme. Br. J. Cancer. 120 (8): 819-826 (2019). PMID 30867563. [link to RRC of NBRP]
user_report Horigome, T., Sulfated glycosaminoglycans and non-classically secreted proteins, basic FGF and epimorphin, coordinately regulate TGF-beta-induced cell behaviors of human scar dermal fibroblasts. J. Dermatol. Sci. 86 (2): 132-141 (2017). PMID 28209294. [link to RRC of NBRP]
user_report Bae, C.R., Overexpression of C-type Natriuretic Peptide in Endothelial Cells Protects against Insulin Resistance and Inflammation during Diet-induced Obesity. Sci. Rep. 7 (1): 9807 (2017). PMID 28852070. [link to RRC of NBRP]
user_report Tomizawa, M., Transcription Factors and Medium Suitable for Initiating the Differentiation of Human Induced Pluripotent Stem Cells to the Hepatocyte Lineage. J. Cell. Biochem. 117 (9): 2001-2009 (2016). PMID 26773721. [link to RRC of NBRP]
user_report Teng, Y.N., beta-carotene reverses multidrug resistant cancer cells by selectively modulating human P-glycoprotein function. Phytomedicine 23 (3): 316-323, 2016. PMID 26969385. [link to RRC of NBRP]
user_report Matsuno, H., A Naturally Occurring Null Variant of the NMDA Type Glutamate Receptor NR3B Subunit Is a Risk Factor of Schizophrenia. PLoS One 10 (3): e0116319 (2015). PMID 25768306. [link to RRC of NBRP]
user_report Emi, Y., Involvement of a di-leucine motif in targeting of ABCC1 to the basolateral plasma membrane of polarized epithelial cells. Biochem. Biophys. Res. Commun., 441 (1): 89-95 (2013). PMID 24129190. [link to RRC of NBRP]
user_report Duff, R.M., Mutations in the N-terminal actin-binding domain of filamin C cause a distal myopathy. Am. J. Hum. Genet. 88 (6): 729-740 (2011). PMID 21620354. [link to RRC of NBRP]