Solute carrier family 22 member 5 (SLC22A5) (NM_003060) Human 3' UTR Clone

Specifications

Product Data
Product Name	Solute carrier family 22 member 5 (SLC22A5) (NM_003060) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CDSP; OCTN2
ACCN	NM_003060
Insert Size	1370 bp
Sequence Data	Insert Sequence (showhide) >SC214131 3’UTR clone of NM_003060 The sequence shown below is from the reference sequence of NM_003060. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCCACAATCCTTAAAAGCACAGCCTTCTAACATCGCTTCCAGTAAGGGAGAAACTGAAGAGGAAAGACT GTCTTGCCAGAAATGGCCAGCTTGTGCAGACTCCGAGTCCTTCAGTGACAAAAGGCCTTTGCTGTTTGT CCTCTTGACCTGTGTCTGACTTGCTCCTGGATGGGCACCCACACTCAGAGGCTACATATGGCCCTAGAG CACCACCTTCCTCTAGGGACACTGGGGCTACCTACAGACAACTTCATCTAAGTCCTAACTATTACAATG ATGGACTCAGCACCTCCAAAGCAGTTAATTTTTCACTAGAACCAGTGAGATCTGGAGGAATGTGAGAAG CATATGCTAAATGTACATTTTAATTTTAGACTACTTGAAAAGGCCCCTAATAAGGCTAGAGGTCTAAGT CCCCCACCCCTTTCCCCACTCCCCTCTAGTGGTGAACTTTAGAGGAAAAGGAAGTAATTGCACAAGGAG TTTGATTCTTACCTTTTCTCAGTTACAGAGGACATTAACTGGATCATTGCTTCCCCAGGGCAGGAGAGC GCAGAGCTAGGGAAAGTGAAAGGTAATGAAGATGGAGCAGAATGAGCAGATGCAGATCACCAGCAAAGT GCACTGATGTGTGAGCTCTTAAGACCACTCAGCATGACGACTGAGTAGACTTGTTTACATCTGATCAAA GCACTGGGCTTGTCCAGGCTCATAATAAATGCTCCATTGAATCTACTATTCTTGTTTTCCACTGCTGTG GAAACCTCCTTGCTACTATAGCGTCTTATGTATGGTTTAAAGGAAATTTATCAGGTGAGAGAGATGAGC AACGTTGTCTTTTCTCTCAAAGCTGTAATGTGGGTTTTGTTTTATTGTTTATTTGTTTGTTGTTGTATC CTTTTCTCCTTGTTATTTGCCCTTCAGAATGCACTTGGGAAAGGCTGGTTCCTTAGCCTCCTGGTTTGT GTCTTTTTTTTTTTTTTTTTAAAACAGAATCACTCTGGCAATTGTCTGCAGCTGCCACTGGTGCAAGGC CTTACCAGCCCTAGCCTCTAGCACTTCTCTAAGTGCCAAAAACAGTGTCATTGTGTGTGTTCCTTTCTT GATACTTAGTCATGGGAGGATATTACAAAAAAGAAATTTAAATTGTGTTCATAGTCTTTCAGAGTAGCT CACTTTAGTCCTGTAACTTTATTGGGTGATATTTTGTGTTCAGTGTAATTGTCTTCTCTTTGCTGATTA TGTTACCATGGTACTCCTAAAGCATATGCCTCACCTGGTTAAAAAAGAACAAACATGTTTTTGTGAAAG CTACTGAAGTGCCTTGGGAAATGAGAAAGTTTTAATAAGTAAAATGATTTTTTAAATAA 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_003060.4
Synonyms	CDSP; OCTN2
Summary	Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is a plasma integral membrane protein which functions both as an organic cation transporter and as a sodium-dependent high affinity carnitine transporter. The encoded protein is involved in the active cellular uptake of carnitine. Mutations in this gene are the cause of systemic primary carnitine deficiency (CDSP), an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation, and later in life by skeletal myopathy or cardiomyopathy. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2015]
Locus ID	6584
MW	51.6

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