SPATA7 (NM_018418) Human 3' UTR Clone

Specifications

Product Data
Product Name	SPATA7 (NM_018418) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	HEL-S-296; HSD-3.1; HSD3; LCA3
ACCN	NM_018418
Insert Size	68 bp
Sequence Data	Insert Sequence (showhide) >SC200065 3’UTR clone of NM_018418 The sequence shown below is from the reference sequence of NM_018418. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AGCATTGAGGACTGCCCTTTGGATGTTTAATCTTCATTAATAAATACCTCAAATGGCCAGTAACTCAA 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_018418.5
Synonyms	HEL-S-296; HSD-3.1; HSD3; LCA3
Summary	This gene, originally isolated from testis, is also expressed in retina. Mutations in this gene are associated with Leber congenital amaurosis and juvenile retinitis pigmentosa. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]
Locus ID	55812
MW	2.3

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