CLN5 (NM_006493) Human 3' UTR Clone
CAT#: SC215321
3' UTR clone of ceroid-lipofuscinosis neuronal 5 (CLN5) for miRNA target validation
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CNY 5,795.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | CLN5 (NM_006493) Human 3' UTR Clone |
Vector | pMirTarget |
ACCN | NM_006493 |
Insert Size | 2000 bp |
Sequence Data |
>SC215321 3’UTR clone of NM_006493
The sequence shown below is from the reference sequence of NM_006493. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATCAGAAACAAAACACTCTCTGGTTTATAAAACACCTTAATTCTACTGCTCTTTTTTCTCCAATCACCA GCATCTGTTTTTCAGGGGGTGATTTTACTTTTGTGAATTCCTTAGCCTTTCTTCCTTGGTGCATAAAGT TAAAATGCACATCAGCAGAATTGCTGCATATTAACATCTCAGGACTCTTCTCTTGTAAAGAAGCTGAAA TTCGTACTATATTGGCCAAAGTGAGCGAGTTAGGTGATCTTGGTTTCAATTTCCGAGCCTTTGTTAATA TGGAGAATTATGGTTCATATCAGTTATGTAGGACCTTTGGACCCAGGGTCCTACAGATAGATATGGTGT GCCCAGATTTTAAAAATACCTTCAAAAATAAAAAATACATTCAGTGACATTTTCATGGTGGGAGCTCTT CTTTCTGATATGGCAGTTACACTTTTTCACTTAAGTGCTTTAGTTTAGACTAACTTTACAACTTCTATA ACTTTTGGAACCAAGTTTAGTATAGTCTGATTACATTCCATTCACCTAACTTTAGACATTCGTTTAGAC ACCATAACTGGAGTGATTGTGCTTCTAGATGTGGCAAATCCAGTGTTAACACATATTTCTGGCTGAGAT TTTGGAACTAGCTAGTAACTGGCTTGTGTTCTTTAAGCATACTAACATCACTAAATCTTAGGATTTAGG ATTGCTGTAAAGATGTAAGTTGTGTATGTTTGGCAGGTCACATTGAATGGCAGTGATAATGATTAATCA AAGAACAAATGTCATCCTTGATCTTGCCTAATGTAGTTTATGTGCCAAACTTTCCAGGGTTTTGTAGTC ACCTAGATTTTAAGCTGATAGCATAGTGCTTCAGCGGTTCTTCTAACCGGGGTATGCAGGAACATGGCT GCAGACACGTTTGGGTAAACAGGCACCTTCTGACTTCTTCATTGTTTCCTGTAGTTCTCCCTCTTCCCA CAAAGCTGTCAGCGCAGTGGAAGAGGTTGCACTTCTCCGAGAGAGGACAGGTTTCTGTTAAGATCACCA AGTAGCTGTGCTTTAATTAGAGCCAGACAAGCTTTCAAGGTCCTTTAAGTATTTGATGATCAACTGAAC ACGTTTCTATTCAAGGAGAAAACACCATTCAGTAAGAAGATGGAGTAGATATCAGATAAAACAATTCAC GTTTAATATGTAAATGTACCAATTATGTGATTCAGTTTCAACTTTCAAGTACTTCCTGAGAGGTTAGTA CATTATTATTGAGCTCTCACAGAAAGCTTAATCATAGATATAATTAACCTGATCCAAATGAGTAAAGTG GACCTTAGAAAGGCTAAGTGATCTTTCTCTGGCTATCCAGCTAGTAGTAATGAAGTCAGGTCTTGAACC CCGGTTCTGCTGACTGAATTGGATGCACTATAGTACAGGCTTTTAGCACCGAAGTGTGGTCCTCAGACC AGTGCCTGCCAACCAGATGTTACTGGTCTGTGAGGAAATAAGTACAGATACTGACAGGAAGCTTTTATA AACAATTTATTGGAGTGTTTTTGTTTCTGTTGGGTCTAATTAAAAAAATTGGAGCTTGTATTTTATGTG TCTTTGGTCTTATTTTGTCTAGGAATTCATTTTTGCTGGGTTTTTTTTTTTCAACTGTAGTCCCACAAC AGTCTGAAAATAACCCAGTCACCAGATATCTTCCTCAAATACAGAGGGAGAACTTTCTTTCACGCCTCC TTTAGCCTGTCGACTCCTTATAATAATGCCTAAATATTCCAAATTAATACTGCCTCTTTAACCTGCTAA TTGTTTTCACAATGTTACAAGAAAACTTGGATCTGTGCATTATCACCATCTAGTGGCTAAACTCAGGCA ACACGAACTTCTACCAAACTCAGGAAATTGCTCTGGAAAAACTACAGGATTTTGGATTTCCAGAACTGC CTTGAAGAGACAAAGATTCTTGTACCAAGTTTTGGTCAACTGCAAATCAAAGAACTTGGTTATGCAGG 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_006493.4 |
Summary | This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.[provided by RefSeq, Oct 2008] |
Locus ID | 1203 |
MW | 75.4 |
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