SIL1 (NM_022464) Human 3' UTR Clone
CAT#: SC205426
3' UTR clone of SIL1 homolog endoplasmic reticulum chaperone (S. cerevisiae) (SIL1) transcript variant 2 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | SIL1 (NM_022464) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | BAP; MSS; ULG5 |
ACCN | NM_022464 |
Insert Size | 423 bp |
Sequence Data |
>SC205426 3’UTR clone of NM_022464
The sequence shown below is from the reference sequence of NM_022464. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GTCAACAGCTTGCTGAAGGAGCTGAGATGAGGCCCCACACCAGGACTGGACTGGGATGCCGCTAGTGAG GCTGAGGGGTGCCAGCGTGGGTGGGCTTCTCAGGCAGGAGGACATCTTGGCAGTGCTGGCTTGGCCATT AAATGGAAACCTGAAGGCCATCCTCTTTCTGCTGTGTGTCTGTGTAGACTGGGCACAGCCCTGTGGCCG GGGGGTCAGGTGAGTGGTTGGGTGATGGGCTCTGCTGACGTGCAGGGCTCAGCCCAGGGCATCCAGGAA CAGGCTCCAGGGCAGGAACCTGGGCCCAGGAGTTGCAAGTCTCTGCTTCTTACCAAGCAGCAGCTCTGT ACCTTGGGAAGTCGCTTAATTGCTCTGAGCTTGTTTCCTCATCTGTCAGGAGTGCCATTAAAGGAGAAA AATCACGTA 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_022464.5 |
Synonyms | BAP; MSS; ULG5 |
Summary | This gene encodes a resident endoplasmic reticulum (ER), N-linked glycoprotein with an N-terminal ER targeting sequence, 2 putative N-glycosylation sites, and a C-terminal ER retention signal. This protein functions as a nucleotide exchange factor for another unfolded protein response protein. Mutations in this gene have been associated with Marinesco-Sjogren syndrome. Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008] |
Locus ID | 64374 |
MW | 14.7 |
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