EIF4H (NM_031992) Human 3' UTR Clone

Specifications

Product Data
Product Name	EIF4H (NM_031992) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	eIF-4H; WBSCR1; WSCR1
ACCN	NM_031992
Insert Size	1818 bp
Sequence Data	Insert Sequence (showhide) >SC216466 3’UTR clone of NM_031992 The sequence shown below is from the reference sequence of NM_031992. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAGGAAGTCGTTCAAAAGGAGCAAGAATGAGCCTGCGGTTGGGAGGGAATGGGGCGTGGGGGGTTAGAG CAGGACCACAGCCTGGTGAGTCCCCGGGCAGCCGTCCTGCAGCCGCCACTCCTGCGCCTGCCATTGGCC TCCTCACAGCGGAAACACAGCTTGTGAGTGCATGTCAGCTGTTAACAAGTGGTTTTTAGTACATTCTGG GCTTTGCTGTATCTATCTAGTGCCTGTTTGTGCGTTTTTTTCTTTCTTCCGCTGCTTCCCCATTTTCCT TCTGTCCTTTTTCTCCTGCTCCTTGTTTTCCCAGCAGCACATGGGGTTCCTCGGAGGAGCAGAGGTGGC CGCCGTGGGGGGGCGTTTGGGCTGCGGTGCTGCGTCATTTTTCCTTTGCTTTCTCTTTACTTTAGACAC TGGCCCAACTCCAGGCGTTTCCTTTCATTCCCTCAGTGCTTCTCTTCTGACCTGCATGTTGAGTTCTGT ATTGCTGGGGCTTCCAACAAAAACCAGAGTCACTGACAGAGGGAACAGCAGAGACCTTGTTGGTATTCA GCTGTGATGGATATAGAGAATCAGAGGCACCTTGTTTTCACAACTAGGATAAAAATATCTGCAGGGTCC TTTCCATTCCTATTTAGAGGGAGTCCTGGCTCCATGACCCCCTCCCGAGTGGACTGTCCAAGCAGATAG GCTCACACGAGAAACAGTGAGGCTGAAAGGGGGGGCTATGGAAGAGCGGTAGGGAGTCCACGGAGAAGA TGCAGTGAATGCTTGCATGCATTCACACGTGTGTGTGTCCCAGCTAGTTCACTCCTTTCGCCGTGCGTG GTGGAGGCTGGCCTCTCTGGCTGGGTGCAGTGAATGGCCAGCGGGTTTCTTTTCTGCTGGGCCAAGGCG CTTTGGGGGTGGAGGGGGTGGTGCTGGTGCTGCACTGGGCTGACTGCGGCGCTGACGCAGCGTTTCCCC CCATCCCTGTTGCCTGTGTGTTGTGTGGATCTGTTCCTAGTATAGGCAACATAATGAGATACTGTGCTT CCCACCTCCCCTTCAGTTCAGAGCCAAAATGGGTCTAGAATCTGGCACTTTACTCATTTCCTTTGATAA ATTGTACTATGCAGAGCTGTCAGGAACCTTCAGATAGCAGTAGAGGACTGCAGCTGTCTAGGTCTGCGG CCACATCTTGGGGACACACTGGACTGTTCCCATGTGCAGGGTTCAGCAGTTATGTGGGAGTGCTAGGGG TTAGGCTTTTGAGCTTGAACGCCTGCGTGTGAACAGATGAAAAATCCTTCAGTACCCAAGTCCCAGTCT GTCCTATGGGGAGCAGTTTGGGGGCGGCCGGCAGCAGGAGCCTGGGAAAGAGGCCCTCGCCAGGTGATG GCAGGGCCAGGGTGGCCTGGGGCACCCAGCGGAATGTGCTTAGTATTTGGTCACCAGCCGTCATCCTGG GCTTTTCCTACTGTGTCTTGTTACAAGGCCTCAGCAATCCACAGAACTCTCTCTCCTTCCTTCCACCTG TCAGCTTCTCTGCTTCTGAGATAAGAACCATTTGTGTAACACCAACACTTAACTTCAGAAAGACATGCA TTATGTGGTGTAATCAAACCCGATGCTTTCAGATGACCTACTTACATCTTCAATGTGGATAAGATAAAG AACAAAACACATGCATCTAAACTGCTGGGCAATCCAGTTGACTTTTAAATGTAAGAATGGAATTCCAAA CACTTAACACATTCAGCTATATGACAGAAAGTAAATCTATGGATATGGTATTTTGTGAATGATCTTTTA AATAAAAGAAAACCTTACGTAATA 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_031992.2
Synonyms	eIF-4H; WBSCR1; WSCR1
Summary	This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq, Jul 2008]
Locus ID	7458
MW	67.7

*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.