GFAP (NM_001131019) Human 3' UTR Clone

CAT#: SC206507

3' UTR clone of glial fibrillary acidic protein (GFAP) transcript variant 2 for miRNA target validation



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CNY 4,845.00


货期*
3周

规格
    • 10 ug

Product images

经常一起买 (2)
Firefly luciferase assay kit, 150 assays
    • 1 kit

CNY 1,520.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1,280.00

Specifications

Product Data
Product Name GFAP (NM_001131019) Human 3' UTR Clone
Vector pMirTarget
Synonyms ALXDRD
ACCN NM_001131019
Insert Size 494 bp
Sequence Data
>SC206507 3’UTR clone of NM_001131019
The sequence shown below is from the reference sequence of NM_001131019. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
GTAAATGGAACGCCGCCGGCTCGCGGTTAGCTGCCTGCCTCTCAGACACGGCGCTTTGCCCAGCTTGAC
AGGGAGTGAGCCTCACCCACCCCATCCTCCCAATCCCCCTGAGTTCCCTCTTCCCAGGCTTCCCCTAAA
GGGCCTGGACTGCGTCATTTTCCCAGGAACTGCAGTGCCCAGCCCAGGACGTGGTACAGAGTAACTGTA
CATTAAACTGGCAGAGCTTGTTAGTGGTAAAGGTGGTGAGTCCTTGGGTGCGCAGTGGAGCTGCTCTGG
GGCCTCTGAGCAAGCAGCAGCCTCTGTCTCACCTCTTCCTGTCACTGGGAGGGCCCCTTGGGTCTCGCT
GTGCCTGGACGCCAGGCTCTCTGCTTTATTCTTTCATCCCTGAGGCTCCATCGCTCAGCTCAGTGCTGA
CTCAGTTCAGAGGATTCTTCCCTCAGGACCGCAGCTCTTGCAGTGAATAAAGTTTTATGTTCCCTGCTC
TTAATGTTAAA
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_001131019.3
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 17.8
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

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