EML1 (NM_001008707) Human 3' UTR Clone

Specifications

Product Data
Product Name	EML1 (NM_001008707) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	BH; ELP79; EMAP; EMAP-1; EMAPL
ACCN	NM_001008707
Insert Size	1978 bp
Sequence Data	Insert Sequence (showhide) >SC217221 3’UTR clone of NM_001008707 The sequence shown below is from the reference sequence of NM_001008707. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ACAAGCATCATGCAGTGGCGCGTCATTTAGTACCCACCGAGAGCTGTGGGGAGCAGCATGGGCAAGGAA GACACAGACTCGCATTACCCTTGGTCACTGTGATTTCTGTTTTGTTTAAAAAATTCTTACAAACCTCAG GAAAACTGTGCCCTCCGCCGGCTACCTTAGCTTAGCGTGTCAGCGGGCGCCACAGCGGATCAGCGGTTC CGTGTTCACTTTTGTTGTACAATATATGACACAGTGCACATTGAATACCAACAAGGTTGCAACGTTTAC ATTATAGCCACATCAACAGAAGTAACTGGTATATTCTTAGTAACTTTTCTATGAACTCTTCAAAAATGG TCACAGAATGCCTTTTAAAACATTGTATATAATCTTCACTGTTTCACCATCTAGCTTGCTAAGTCAAAT ATTTATGATGATAATGAGGTACTGAACCACGATGGCTGTTGAGGAATTGGTCCTAAAAGGACAGATCAC TTCAGAAGAGTGAATAACTGATTTGCACAGCTGAATCAGGAGACACAAAGATGAGACTGTGTTTGGTTA CATTTTCCAAAGTTTCATTGCATTCTCCCTTGGGGAGGCTGTGAGAGAGGGCTTGTATCCCTCTTGTGC TAAGCAGACTCTACTCCTAACTGACTTCAATATTTCAGCAGGGTACACAGGCGTTTCCAAGTTTCAGTG ACACCGTCCTGCCTAACCAGATGCGGTCAGCCTCTTCACACCCACCTGGCTTGCATCCCCCATCCCTTG TTCACACGCCCTGATTCACGGTGAGACATTTTGCCACCTTCTTGTGTATATTACTTGGCATGAGATGAT ATTGTACTTGTATAGGATTCTAGCAATTCATAATAAATATGTAAGACTAGGCTTTACTGTCTTATGCTT ATGGACATTGTATATTTGTATTTTATGACCAAGTAGACCAAGTCAGAAAGATCTCTCTCGAGCGTACCA TAAACCTGCAGAGAGAAGTCTCGAAAGGCTCCACCAGGTACCAAGGGCAGCTGCTTTTCCTGTCTTTTG TGCATGGGCGACCCATTACAGTATGAGATAAGATTGAGTTCTGATGCGTTAAACGGAGGTGGCAGAAAT TTGTCAAGAAGGCCTTATCCATTTCGATTGTGTGACAGATTGAAATTTATTGTTTACATTGGGGAATGT ATCTCAAATTTTTAAATAGAAGAGTAATAAACAGACTTTAAAGCAAATATTAAGATTTTTACTCATTCA AGGCAAGTAAATGAATGGAATTATCTGAGCTCTATGGCACTGGTTGTTTAGAGTGACTGATGAAGTGCA ACTTTCAAAAACATTTTTGATGACATCACCAGCCTACTGCAGAAGTGCAGGGCACCAGTAAACACCATG TATTATTGAAGATGAATCTGTTTGTATGTATCCTTGTCAAATATATTCTATAATGAAATAAAATCTGAA AAGTGGATTTCTTATTGACCTATATTCATGAAAGCATATAAATTAAAATATTTAAAATTAGATATGATT CACACTATATTCTGTTTCATATGCAGATTTTATTCTCACCTGGGCCATTTGCAGATGAGACTGTAGTTT GCAGATGAGACTGTAGTTTGCAGATGGCGTGGAAGCATTCATCAGGGGAGATAACCATAAAGGATTTGG CCTAATTACCATACTCAATTGTCAGTTTACGTGGTTTTGTGAATACTGGCAAAAGCAATTGTTTTTAAA TTAACAATGGAGAGAATGATAAGATGAGGGAAGGAAAAGGCATTCATTATTGACTTACATGTCAGTAAG GTCTGCTTTTATTTCTATGTACTCCTGTTTGCCAAGCTCAATAATGGACAAAGGATACAAACACACACA CATCTACTATTTTAGATAAATGTACTGTTATATATATATGTAAACTACTATTGCTCTCTTTATAATGAT TAATCACTTTATTATGAATGAATGAATGAATTTGATGGATTTAAAA 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_001008707.2
Synonyms	BH; ELP79; EMAP; EMAP-1; EMAPL
Summary	Human echinoderm microtubule-associated protein-like is a strong candidate for the Usher syndrome type 1A gene. Usher syndromes (USHs) are a group of genetic disorders consisting of congenital deafness, retinitis pigmentosa, and vestibular dysfunction of variable onset and severity depending on the genetic type. The disease process in USHs involves the entire brain and is not limited to the posterior fossa or auditory and visual systems. The USHs are catagorized as type I (USH1A, USH1B, USH1C, USH1D, USH1E and USH1F), type II (USH2A and USH2B) and type III (USH3). The type I is the most severe form. Gene loci responsible for these three types are all mapped. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Locus ID	2009
MW	76.9

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