RPGR (NM_000328) Human 3' UTR Clone
CAT#: SC206290
3' UTR clone of retinitis pigmentosa GTPase regulator (RPGR) transcript variant A for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | RPGR (NM_000328) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | COD1; CORDX1; CRD; orf15; PCDX; RP3; RP15; XLRP3 |
ACCN | NM_000328 |
Insert Size | 493 bp |
Sequence Data |
>SC206290 3’UTR clone of NM_000328
The sequence shown below is from the reference sequence of NM_000328. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AGAAGATCAAAATCCTGTACAATACTATAAATATATATTTATGTTTTCACAGTCACCAAGTGTATTGTA ATGTATACTTGAAAAATGTTATAACTTATGAAGTAAAGTTTCTGATAGTAGTCTTTAAAAGATATAAGA CTTAATATGTTTTATTCAGCTTCTATAAGTGTGACCAGTTTTGATATTTATTTATGCTAATATTTTTAA CAAGTCATTTCAAAATATGTGTATCTCAAATTCTCCCTAAAGTGTTGTGGCCTTAACTGTTCAGTATTG CAATAAAAAATATATTTTTATATGTGGAAAATTGAAATAAGATATTTCCTAGTTTTTACTAAACAATTT TACTTCTTTATAATTTTATAAGGCAATATTTGCAATCTTACGACACTGTAACAGTTTTTGATGTATTTA CAATTTTTACAAAACTGAGGTAAAATTGTTTATAATGAACATATTTTAATAAACTATATCTGGTCAGTT CCACTGTTAA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG |
Restriction Sites | SgfI-MluI |
OTI Disclaimer | Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs). |
Reference Data | |
RefSeq | NM_000328.3 |
Synonyms | COD1; CORDX1; CRD; orf15; PCDX; RP3; RP15; XLRP3 |
Summary | This gene encodes a protein with a series of six RCC1-like domains (RLDs), characteristic of the highly conserved guanine nucleotide exchange factors. The encoded protein is found in the Golgi body and interacts with RPGRIP1. This protein localizes to the outer segment of rod photoreceptors and is essential for their viability. Mutations in this gene have been associated with X-linked retinitis pigmentosa (XLRP). Multiple alternatively spliced transcript variants that encode different isoforms of this gene have been reported, but the full-length natures of only some have been determined. [provided by RefSeq, Dec 2008] |
Locus ID | 6103 |
MW | 19.8 |
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