STRA6 (NM_001142618) Human 3' UTR Clone

Specifications

Product Data
Product Name	STRA6 (NM_001142618) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	MCOPCB8; MCOPS9; PP14296
ACCN	NM_001142618
Insert Size	644 bp
Sequence Data	Insert Sequence (showhide) >SC208154 3’UTR clone of NM_001142618 The sequence shown below is from the reference sequence of NM_001142618. 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_001142618.2
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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