STRA6 (NM_001142617) Human 3' UTR Clone
CAT#: SC208155
3' UTR clone of stimulated by retinoic acid gene 6 homolog (mouse) (STRA6) transcript variant 1 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 | STRA6 (NM_001142617) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | MCOPCB8; MCOPS9; PP14296 |
ACCN | NM_001142617 |
Insert Size | 644 bp |
Sequence Data |
>SC208155 3’UTR clone of NM_001142617
The sequence shown below is from the reference sequence of NM_001142617. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTGTTGGGTGCCAATGGTGCCCAGCCCTGAGGGCAGGGAAGGTCAACCCACCTGCCCATCTGTGCTGAG GCATGTTCCTGCCTACCATCCTCCTCCCTCCCCGGCTCTCCTCCCAGCATCACACCAGCCATGCAGCCA GCAGGTCCTCCGGATCACTGTGGTTGGGTGGAGGTCTGTCTGCACTGGGAGCCTCAGGAGGGCTCTGCT CCACCCACTTGGCTATGGGAGAGCCAGCAGGGGTTCTGGAGAAAGAAACTGGTGGGTTAGGGCCTTGGT CCAGGAGCCAGTTGAGCCAGGGCAGCCACATCCAGGCGTCTCCCTACCCTGGCTCTGCCATCAGCCTTG AAGGGCCTCGATGAAGCCTTCTCTGGAACCACTCCAGCCCAGCTCCACCTCAGCCTTGGCCTTCACGCT GTGGAAGCAGCCAAGGCACTTCCTCACCCCCTCAGCGCCACGGACCTCTCTGGGGAGTGGCCGGAAAGC TCCCGGGCCTCTGGCCTGCAGGGCAGCCCAAGTCATGACTCAGACCAGGTCCCACACTGAGCTGCCCAC ACTCGAGAGCCAGATATTTTTGTAGTTTTTATGCCTTTGGCTATTATGAAAGAGGTTAGTGTGTTCCCT GCAATAAACTTGTTCCTGAGAAA 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_001142617.2 |
Synonyms | MCOPCB8; MCOPS9; PP14296 |
Summary | The protein encoded by this gene is a membrane protein involved in the metabolism of retinol. The encoded protein acts as a receptor for retinol/retinol binding protein complexes. This protein removes the retinol from the complex and transports it across the cell membrane. Defects in this gene are a cause of syndromic microphthalmia type 9 (MCOPS9). Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Dec 2008] |
Locus ID | 64220 |
MW | 22.5 |
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