PTDSS1 (NM_014754) Human 3' UTR Clone

Specifications

Product Data
Product Name	PTDSS1 (NM_014754) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	LMHD; PSS1; PSSA
ACCN	NM_014754
Insert Size	2000 bp
Sequence Data	Insert Sequence (showhide) >SC211537 3’UTR clone of NM_014754 The sequence shown below is from the reference sequence of NM_014754. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AAAGTCACCAATGGCGTTGGAAAGAAATGAAAAACCCTGGTTAATCAAAGATGTTCCAGAGTGCCTAGA ACTGAGAGGGAAATGGAACTCATTTGGAACTCCCCGTGAGGAGGTCGAGGCGCACAGGGCAAGCAGGAA GAGGCGAGGGCACTTGGGGGTCATTATTTGAGATCGTAAGTCTTGTTTCCCACAGACCTGGCCGCGTCA GGCAGATCATCGCCTGGGGGGCCTTTGCCAACGTGGGGTCTCTTCTAACTTCAGCACTTGACATGCGGT CACCGGTGGCAGCGCGGTGTGTTGAAGGGAAACGGTAGCTATTCATTCACAGTTGCCAAGAGCAGCTCC GCGCCTGCTGGATCGTGGATGCAGCGTAAACATCTTCCTTCAGACGAGGCATTAACCCCATGGTTAATG GACTGGTCACCAGTTTTTATTTTATTTTTATGAATCTACCTTTCCATTGATTGATTTAAGTTCAGGCCA CTTTTCTGTCTTTTATTTGGTTACTGTTGTTATTTGTTTTTAAGTTAGGATGCTTTTTAACAGCCTTTA GAAGCCGCTGCTGAAATTGATACTGGGGGAAGGGTTCCCCTTCCTTCTAGAGCAGAAAAGGGAGAGAGG TGTTGTATTCCTGTTTGGTAACCTCAGTCTCCTGTAAGACCTCCTACCACATGGCGAGTATACACCAAT CAGGAGAGGGTAGCTGCCTGCATAGGAGCCTCGCTTCCGATTATTCCCTTCCCAATATTATTCATCCAG ACTTAGCCACAGTGCACAAAAGCAAACCTGCTAGAGAGGCAGTGAACACCACAGCTTCTCCCCAGCTAG GTGCCTTTTACATCGGGTTTGTTCTCCTTCCATGGTGTGTTGCTGACATTGTCACTGAGTCCCATGTGA GGTGCTGGTGAGTATTACCTTTCATCTGTGCCATGCTCTAGAACCTTGACCTTGATAGTTCACCACCTC TGATGGATCCCTGTTTTAAATAAAAACGATTCACTTTAAAGCCTATCAAAGGTCTGTCTGTAAAATGCT CATTTTCTTGCATCTTACTGGTATCTTCTATTGATTGTAAGCAGTCTGTGTTTTTCAAGTGACTTTAGG ATAATATATATGTGTTTTACATAGTGAGAAGAAAAAAGAAAAGATGTGTATTTTAAAGGGCTTACAGAC ATATATGTCCTACTTCTTAGACTACCCAAGTGACCAACAGGAATGAACAACATAGTCATTGTTTTTTCC TGTGGTAATGGTTTCCAAGTTGGACTTTTTTTTCCTCTAACAAGAGGCCAGTACCCAGTTGATTAGCTT ACAGATATCAACTCACTGAAAGTAATCTTTTGTTCCCTCATTTCACACAGCACAAAGGTTCGTTCTGAT GTTTCTTCTTCTTTAAGGAAATCTTTAGCCATAGAAGTGTCACTTTTTTTTTTTCTGCAAAAGAATTCC AAGATGAACGGGTTGAATGAATCATGCCAGCCAGGGTCACATCCTGTCCTCAGGGGGCCCAGTGCTCAA TAGTAGATTCTGCGGGAGTGGAGAAGCGTCAGTGGCAGCTCCGCTCACTTGGTGAGTGAGGGATTTGGC TGTGATGAGCCTCAGCTCCGAGCTCTCAAATGTCCTCCAGCCAGCATCTGCCTGCTTCCCACAAAAGGA TAGAAGAGAGGCAAAGTGCGTGTTTCATAAAACCTGCCTGCACTTTTATAACCCATCAAAGAGGCCATT TTTAAACACAGGTACAATTTAAACATGATCTTTCTTTGCAAATAAATATGTTTTGTTTCATCCTGTGTT CTGCTTTTCTAAGCATGACATACTTGTGCCCATTGGAGAAGACACCTGTCTCTTCTTTCTCACACCGGT GGTGCCTCACTGAGTGTTTCCGGGTTCATTTTCCGGGAGCACTGGGCCTGACACTTTCACACTCTTCTG ACTTTCGCCTTGTTGCAACTGATGGAGCATGTGTGCTTCCTCTGAGGCCAGCCTACAGGAGGCAGCTG 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_014754.3
Synonyms	LMHD; PSS1; PSSA
Summary	The protein encoded by this gene catalyzes the formation of phosphatidylserine from either phosphatidylcholine or phosphatidylethanolamine. Phosphatidylserine localizes to the mitochondria-associated membrane of the endoplasmic reticulum, where it serves a structural role as well as a signaling role. Defects in this gene are a cause of Lenz-Majewski hyperostotic dwarfism. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2014]
Locus ID	9791
MW	74.4

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