GFAP (NM_002055) Human 3' UTR Clone
CAT#: SC216173
3' UTR clone of glial fibrillary acidic protein (GFAP) transcript variant 1 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 | GFAP (NM_002055) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | ALXDRD |
ACCN | NM_002055 |
Insert Size | 2000 bp |
Sequence Data |
>SC216173 3’UTR clone of NM_002055
The sequence shown below is from the reference sequence of NM_002055. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TCCAAGCAGGAGCACAAGGATGTGATGTGAGGCAGGACCCACCTGGTGGCCTCTGCCCCGTCTCATGAG GGGCCCGAGCAGAAGCAGGATAGTTGCTCCGCCTCTGCTGGCACATTTCCCCAGACCTGAGCTCCCCAC CACCCCAGCTGCTCCCCTCCCTCCTCTGTCCCTAGGTCAGCTTGCTGCCCTAGGCTCCGTCAGTATCAG GCCTGCCAGACGGCACCCACCCAGCACCCAGCAACTCCAACTAACAAGAAACTCACCCCCAAGGGGCAG TCTGGAGGGGCATGGCCAGCAGCTTGCGTTAGAATGAGGAGGAAGGAGAGAAGGGGAGGAGGGCGGGGG GCACCTACTACATCGCCCTCCACATCCCTGATTCCTGTTGTTATGGAAACTGTTGCCAGAGATGGAGGT TCTCTCGGAGTATCTGGGAACTGTGCCTTTGAGTTTCCTCAGGCTGCTGGAGGAAAACTGAGACTCAGA CAGGAAAGGGAAGGCCCCACAGACAAGGTAGCCCTGGCCAGAGGCTTGTTTTGTCTTTTGGTTTTTATG AGGTGGGATATCCCTATGCTGCCTAGGCTGACCTTGAACTCCTGGGCTCAAGCAGTCTACCCACCTCAG CCTCCTGTGTAGCTGGGATTATAGATTGGAGCCACCATGCCCAGCTCAGAGGGTTGTTCTCCTAGACTG ACCCTGATCAGTCTAAGATGGGTGGGGACGTCCTGCCACCTGGGGCAGTCACCTGCCCAGATCCCAGAA GGACCTCCTGAGCGATGACTCAAGTGTCTCAGTCCACCTGAGCTGCCATCCAGGGATGCCATCTGTGGG CACGCTGTGGGCAGGTGGGAGCTTGATTCTCAGCACTTGGGGGATCTGTTGTGTACGTGGAGAGGGATG AGGTGCTGGGAGGGATAGAGGGGGGCTGCCTGGCCCCCAGCTGTGGGTACAGAGAGGTCAAGCCCAGGA GGACTGCCCCGTGCAGACTGGAGGGGACGCTGGTAGAGATGGAGGAGGAGGCAATTGGGATGGCGCTAG GCATACAAGTAGGGGTTGTGGGTGACCAGTTGCACTTGGCCTCTGGATTGTGGGAATTAAGGAAGTGAC TCATCCTCTTGAAGATGCTGAAACAGGAGAGAAAGGGGATGTATCCATGGGGGCAGGGCATGACTTTGT CCCATTTCTAAAGGCCTCTTCCTTGCTGTGTCATACCAGGCCGCCCCAGCCTCTGAGCCCCTGGGACTG CTGCTTCTTAACCCCAGTAAGCCACTGCCACACGTCTGACCCTCTCCACCCCATAGTGACCGGCTGCTT TTCCCTAAGCCAAGGGCCTCTTGCGGTCCCTTCTTACTCACACACAAAATGTACCCAGTATTCTAGGTA GTGCCCTATTTTACAATTGTAAAACTGAGGCACGAGCAAAGTGAAGACACTGGCTCATATTCCTGCAGC CTGGAGGCCGGGTGCTCAGGGCTGACACGTCCACCCCAGTGCACCCACTCTGCTTTGACTGAGCAGACT GGTGAGCAGACTGGTGGGATCTGTGCCCAGAGATGGGACTGGGAGGGCCCACTTCAGGGTTCTCCTCTC CCCTCTAAGGCCGAAGAAGGGTCCTTCCCTCTCCCCAAGACTTGGTGTCCTTTCCCTCCACTCCTTCCT GCCACCTGCTGCTGCTGCTGCTGCTAATCTTCAGGGCACTGCTGCTGCCTTTAGTCGCTGAGGAAAAAT AAAGACAAATGCTGCGCCCTTCCCCAGAGTGGACTCTGATCTGTTCATGAGAGGGCGGGACTGGGGCCA AGATGTAGCCTTTGACAAGACCAACTCATTTCTTATTACTGATCATCTCTGGGGCCCATGCCCTCACCA AATTCCACCCGCAGCCAAAGAGGACATACACCAGCTCCCTCCACTCTTTTCTTCCTTCCTCTCCCTGCT ACCTGCAACTCAACCAGCACAATCTTCATAGGCAAGAAAGCAAAGCAGCTCAAACATGATTCAACACT 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_002055.5 |
Synonyms | ALXDRD |
Summary | This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008] |
Locus ID | 2670 |
MW | 72.3 |
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