NTAL (LAT2) (NM_032464) Human 3' UTR Clone

Specifications

Product Data
Product Name	NTAL (LAT2) (NM_032464) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	HSPC046; LAB; NTAL; WBSCR5; WBSCR15; WSCR5
ACCN	NM_032464
Insert Size	939 bp
Sequence Data	Insert Sequence (showhide) >SC211074 3’UTR clone of NM_032464 The sequence shown below is from the reference sequence of NM_032464. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AATGGGGAGGTGGCAGCCACAGAAGCCTAGGGCAGACCAAGAAGAAAGGAGCCAAGGCAAAGAGGGACC ACTGTGCTCATGGACCCATCGCTGCCTTCCAAGGACCATTTCCCAGAGCTACTCAACTTTTAAGCCCCT GCCATGGTTGCTCCTGGAAGGAGAACCAGCCACCCTGAGGACCACCTGGCCATGCGTGCACAGCCTGGG AAAAGACAGTTACTCACGGGAGCTGCAGGCCCGTCACCAAGCCCTCTCCCGACCCAGGCTTTGTGGGGC AGGCACCTGGTACCAAGGGTAACCCGGCTCCTGGTATGGACGGATGCGCAGGATTTAGGATAAGCTGTC ACCCAGTCCCCATAACAAAACCACTGTCCAACACTGGTATCTGTGTTCTTTTGTGCTATGAATTTGGAT TCCTAATTGCTATTGTTGGTTGCTGGGGTTTTAAATGATTGATAAGCTTGTACAGTTAACTTATAGAGG GGGAGCCATATTTAACATTCTGGATTTCAGAGTAGAGATTTCTGTGTTGTCTCCTAGAAAGCATTACAT GTAGTTTATTTCAGCATCCTTGTTGGGTGGGGCCCTGGCTCTCTTCCCCTTTGGTGGGACCTCCCCTTT CTTTGGGCTTCAGTTCACTCAGGAAGAAATGAGGCTGTCGCCATCTTTATGTGCTTCCAGTGGAAATGT CACTTGCTACAGACAATAGTGCATGAGAGTCTAGAGAAGTAGTGACCAGAACAGGGCAGAGTAGGTCCC CTCCATGGCCCTGAATCCTCCTCTGCTCCAGGGCTGGCCTCTGCAGAGCTGATTAAACAGTGTTGTGAC TGTCTCATGGGAAGAGCTGGGGCCCAGAGGGACCTTGAGTCAGAAATGTTGCCAGAAAAAGTATCTCCT CCAACCAAAACATCTCAATAAAACCATTTTAGTTGAAAAGCA 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_032464.3
Synonyms	HSPC046; LAB; NTAL; WBSCR5; WBSCR15; WSCR5
Summary	This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein. [provided by RefSeq, Jul 2008]
Locus ID	7462
MW	34.3

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