NTAL (LAT2) (NM_032463) Human 3' UTR Clone
CAT#: SC211071
3' UTR clone of linker for activation of T cells family member 2 (LAT2) transcript variant 2 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 | NTAL (LAT2) (NM_032463) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | HSPC046; LAB; NTAL; WBSCR5; WBSCR15; WSCR5 |
ACCN | NM_032463 |
Insert Size | 939 bp |
Sequence Data |
>SC211071 3’UTR clone of NM_032463
The sequence shown below is from the reference sequence of NM_032463. 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_032463.3 |
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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