ARSA (NM_000487) Human 3' UTR Clone
CAT#: SC201269
3' UTR clone of arylsulfatase A (ARSA) transcript variant 1 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 | ARSA (NM_000487) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | ASA; MLD |
ACCN | NM_000487 |
Insert Size | 2000 bp |
Sequence Data |
>SC201269 3’UTR clone of NM_000487
The sequence shown below is from the reference sequence of NM_000487. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TGCTGCCATTGCCCAGATCCCCATGCCTGAGGGCCCCTCGGCTGGCCTGGGCATGTGATGGCTCCTCAC TGGGAGCCTGTGGGGGAGGCTCAGGTGTCTGGAGGGGGTTTGTGCCTGATAACGTAATAACACCAGTGG AGACTTGCAGATGTGACAATTCGTCCAATCCTGGGGTAATGCTGTGTGCTGGTGCCGGTCCCCTGTGGT ACGAATGAGGAAACTGAGGTGCAGAGAGGTTCAGGACTTGTACAAGATCACCCAGCCAGAAAGAGGTTG GGCTGGGATTTGAACCCTGGTGTCGTGGCTCTGGAAGCTGCCCTGGCGCCTTGGTGATCTGCGTGGGTC AGTGCACACAGGCACACGTCAGCCTCAAGGACATGGGCACATCTGTTCACAGGAGCAGCGCCACGTGCC TTTGAGTGCCAGGAACGGGGTGGGAGGGTGGGAGGGTGTGAGGGCCAGAAGACTCAGAAGATGCAAAGT GCCTGAGAGAGACGGGATATTCCCCCAGAAGAAGCATTCTTAGAGACACAGGCACTGGACCTCCTTGGT TCTTATAAGAAACCTGTCTGAAGCTGGGTGATGAGTTGCACACTCCAGGTGGGGCTAAGGGGCCTGGAG CCCCTGCTGGCTCCTAGGAAGGCACAGCAGCAGGCCCTGAGACGGCTCCTCTGGGGCCCCTCCACCCTC CCAGGCCTCTGCATTTCACCTGTGCCCACACTTCTGTCTCCTGCCTTCACCTTTTGACCCACTACTAAC GATTCTCCACCCAGCAGACAAAGTGATCTCTTAAAAATATCTGTTGGCTGGGCACGGTGGCTCACGCCT GTAATCCCAGCACTTTAGGAAGCCGAGGCGGGTGGATCACCTGAGGTCGGGAGTTCGAGACCAGCCTGA CCAACATGGAGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAGGTGTAGTGGTGCATCCCTGTAA TCCCAGCTACTTGGGAGTCTGAGGCTGGAGAATCACTTGAACCTGGGAGGCGGTGGTTGCAGTGAGCCG AGATCGCACCATTGCACTCCAGCCTGGGCAACAAGAGAAAAACTCTGTCTCAAAAAACAAAAAATCTGT TAGGCTGCACACGGCGATTCACTCCTGTATTCCCAGTGCTTTGGGAGGCTGAGGTGAGAGGATGCCTGA GGCCAGGAATTCAGACCAGCCTGGGCAACATAGTGAGACCCCAGCTCTAAAGATTTGTTTTTGTTTTTT TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTAGAGT GCAGTGGTACCATCTCCGCTCACTGCAACCTCCGCCTCCCGGGTTCCAGGGATTCTCCTGCCTCAGCCT CCCTAGTAGCTGGAACTACAGGTGTGTGCTGCCATGCCCAGCTAATTTTTTTTTATTTAATAGAGACAA GATTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCACCCGCCTCAGCCTCCC AAAGTGCTGGGATTACAGGTGTGAACCACCACACCTGGCCAACAATATTTGTTTTAATTAGCCAGGCGT GGTAGCATTTGTCCTAGCAATTTGGGAGGTTGAGGTGGGAGAATCACTTCAGCCCACTAGGTCGAGGCT GTAGTGAGCTATAATTGTACCACTGCACTCCAGCCTCGGGGACAGAGTGAGACCCTGTCTGCAAATAAA CAAATAAAACATCAGGCTGGGCTTGAGCATCTATTCCTGCTCAAAATTTCGCAGGCTTCTCAGAAGAAA ATCCAAACCCCTTACAGTGACCCAGTTTGCCCTTGAGGCCTCCACCCACACCCCCTTCCCCCCAGTCTT AGGGGGTGGCCTGGCTGTTCCCTTCAACGGCAACGCTCTGCCTCCATTGTTGGCCTCCTCTGCAGGGAG GGACTGTCTGAGCACCTGCCCGTGTCTGTGCAGCATGGCACACTGACGTCAGGCCCACGTGCATGCCC 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_000487.6 |
Synonyms | ASA; MLD |
Summary | The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy (MLD), a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Dec 2010] |
Locus ID | 410 |
MW | 72.5 |
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