ABHD11 (NM_148916) Human 3' UTR Clone

Specifications

Product Data
Product Name	ABHD11 (NM_148916) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	abhydrolase domain containing 11; PP1226; WBSCR21; Williams Beuren syndrome chromosome region 21
ACCN	NM_148916
Insert Size	439 bp
Sequence Data	Insert Sequence (showhide) >SC205499 3’UTR clone of NM_148916 The sequence shown below is from the reference sequence of NM_148916. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TTGGCCCAGCAGACAGGCCGTAGGGGATGACCGGGAGCTCACCACCTCTTATGGCAGCCCATTCTTCTG TGCTCCTACTGTTGGAAATTCCTGGAGTCTCCTTCCTGGCATTCTCCGAGATTGCCACCCAGCCAGGCC AGCCCTTCAGAGACGTGGTCACAACCCTGGGGCCTGCTCTTCTCTGGCAGAGTGGCCCCAGGTTCTTCA TCTGGGCCTCCTAGGTCTGGAAACTGGGCCCTTCCCCTCCACAGGGTGTATCCCCAGGCTCTCCACACC TTTGACCTGCTGTCCCTACAAGCCTTTGGCTGTCTACCCCCAGAATGGGGATATCAACGCAGCCCCGTC TCACCCCACTCCCCAGGTGCTGACGGTGGATGCTCGTAACCACGGTGACAGCCCCCACAGCCCAGACAT GAGCTACGAGATCAAAAAAAAAAAA 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_148916.3
Synonyms	abhydrolase domain containing 11; PP1226; WBSCR21; Williams Beuren syndrome chromosome region 21
Summary	This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Mar 2016]
Locus ID	83451
MW	16.2

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