ST3GAL5 (NM_003896) Human 3' UTR Clone

Specifications

Product Data
Product Name	ST3GAL5 (NM_003896) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	SATI; SIAT9; SIATGM3S; SPDRS; ST3Gal V; ST3GalV
ACCN	NM_003896
Insert Size	2000 bp
Sequence Data	Insert Sequence (showhide) >SC211780 3’UTR clone of NM_003896 The sequence shown below is from the reference sequence of NM_003896. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTCAGTGGAGGCATTGATCGTGAATTTTGAACACAGAAAACCTCAGTTGAAAATGCAACTCTAACTCTG AGAGCTGTTTTTGACAGCCTTCTTGATGTATTTCTCCATCCTGCAGATACTTTGAAGTGCAGCTCATGT TTTTAACTTTTAATTTAAAAACACAAAAAAAATTTTAGCTCTTCCCACTTTTTTTTTCCTATTTATTTG AGGTCAGTGTTTGTTTTTGCACACCATTTTGTAAATGAAACTTAAGAATTGAATTGGAAAGACTTCTCA AAGAGAATTGTATGTAACGATGTTGTATTGATTTTTAAGAAAGTAATTTAATTTGTAAAACTTCTGCTC GTTTACACTGCACATTGAATACAGGTAACTAATTGGAAGGAGAGGGGAGGTCACTCTTTTGATGGTGGC CCTGAACCTCATTCTGGTTCCCTGCTGCGCTGCTTGGTGTGACCCACGGAGGATCCACTCCCAGGATGA CGTGCTCCGTAGCTCTGCTGCTGATACTGGGTCTGCGATGCAGCGGCGTGAGGCCTGGGCTGGTTGGAG AAGGTCACAACCCTTCTCTGTTGGTCTGCCTTCTGCTGAAAGACTCGAGAACCAACCAGGGAAGCTGTC CTGGAGGTCCCTGGTCGGAGAGGGACATAGAATCTGTGACCTCTGACAACTGTGAAGCCACCCTGGGCT ACAGAAACCACAGTCTTCCCAGCAATTATTACAATTCTTGAATTCCTTGGGGATTTTTTACTGCCCTTT CAAAGCACTTAAGTGTTAGATCTAACGTGTTCCAGTGTCTGTCTGAGGTGACTTAAAAAATCAGAACAA AACTTCTATTATCCAGAGTCATGGGAGAGTACACCCTTTCCAGGAATAATGTTTTGGGAAACACTGAAA TGAAATCTTCCCAGTATTATAAATTGTGTATTTAAAAAAAAGAAACTTTTCTGAATGCCTACCTGGCGG TGTATACCAGGCAGTGTGCCAGTTTAAAAAGATGAAAAAGAATAAAAACTTTTGAGGAACTCTCGTAGT CTGGTTAATTTGGGTGCTTATGTCTATGAATCTACCCAAAACCTCCTTCTTGGATGCTGCTGCTAGGCG GAGACCTCTCTGTGGATGCCAGTAGTGAGGGACAGAGAATTAAGGCACCTGGTCCTGCAAGCTGCTTGA GTCCAGACAACTGTGAACCCTTCTGAAGAGATGCTGGGTGTCGGTGGCTTCCTCCCCAAAGACAGGCTG CCCCTAGCTTCTGTCTCTTAATGGCTCTAGCCTCTGATATCAGAAGATCTGCTACTCTGTTCCCAGCCT GCCCCAGACTCGGCTGCCGCCATCGCTGTTCTCCACTCTGTGGCTGCTCTTGTCACTAATGCTACCTGC CTCCACTTTCCCTTCCTGCAACTGCTTGTGCAGCCCCAGTGCAGCCTTGGCCCCAGCCCATTCGAACGT CTTCCCATCTCCCTCCTCCTCACCATATGCAGGGCCAGGAGTCAGGTCATAGCATTCAAAGCAGAGTCC CTTCTGTCTCCTGGGGTCTGGGATCCAGCTCAGAGTGGCCAGGAGAGCAAAAGTCATATTTCTCTCGTT TTGTGTCTTTACAGATAATTTTGTATGAATTTTATTTCCTACTCTATAAGCTACTGCTTGTTTAAGAGA AAATGTTTTAAGATTATCACCCATCAAATGAGTTTAGAAAATTGAGACTCTGGAAGATGGTCCACAGCT CCCTTGTGGCTCAGGTGGTGCTGGGCTTACACCACACAGCTCCACCCCTACATCCCTCAGGGGGTTATT GGAGAAGCCGGAACTTCCTCAGACAACGTTCTTAATGCTACGAGCGCCTCCTTGCTGGTATGAGGAGAC TTGCCTACCTGCTTCTCAAGGCTGCTGGGATGTGTGGTGCTCAAAGCTTCCACTTGGTCAGCTTGCAGC CATTCTCAGGCCTGCTCCCATCCCCATCCCTCCTCCCTGTAAGGCCCTTCTTGCATCCTTAGGTTGCT 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_003896.4
Synonyms	SATI; SIAT9; SIATGM3S; SPDRS; ST3Gal V; ST3GalV
Summary	Ganglioside GM3 is known to participate in the induction of cell differentiation, modulation of cell proliferation, maintenance of fibroblast morphology, signal transduction, and integrin-mediated cell adhesion. The protein encoded by this gene is a type II membrane protein which catalyzes the formation of GM3 using lactosylceramide as the substrate. The encoded protein is a member of glycosyltransferase family 29 and may be localized to the Golgi apparatus. Mutation in this gene has been associated with Amish infantile epilepsy syndrome. Transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Locus ID	8869
MW	74.5

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