Bestrophin (BEST1) (NM_001139443) Human 3' UTR Clone
CAT#: SC206279
3' UTR clone of bestrophin 1 (BEST1) transcript variant 2 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
Product images
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经常一起买 (2)
Specifications
Product Data | |
Product Name | Bestrophin (BEST1) (NM_001139443) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | ARB; BEST; Best1V1Delta2; BMD; RP50; TU15B; VMD2 |
ACCN | NM_001139443 |
Insert Size | 2000 bp |
Sequence Data |
>SC206279 3’UTR clone of NM_001139443
The sequence shown below is from the reference sequence of NM_001139443. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GACTTCTTGGGACCAGGTGAAGGAAGATGAGGTTGTGCTGACCAGAATGCTGCTGGAGAACTGCCCCAG GGCTGACAGGCCAGGCTTAGCTGAGCAGATGTTATCACTGGCCCCAACTTACTTTGAGCAAGGGTGGCT GACCCAAAACCATGAGGTGGCAGTCAGCTGGATGACAGATGAACACTTCCCCCATAACTATTTAGGGTA GTACCCAAGCACTACAGGAAAGGGTGGCAGGAACTGCCTCACTCCTAGGAACTGGTAGATGGTGAGGTT GAGGGTGTCCAGCGCCCTTAGGTCATTTTCTCACTGCCTGGGAACCTCACCAAAATACTTCTTGCTTCC TTGGGGTCAGCCCAAAGCTGTCACAAAATCAGATATTTCCCTTTATTCCAGATTTCCTGGACACTTTCA CCCAATTATAAACACCCCACTTCAGCCCCAATCACGTGGGAGGAAGTGTAACTTCCCTTTTCTGGATTC TCAAGCAGTTACTTTCACGGTCAGAACACGCAGCTATTATGATTGAAAACTTAAAAGGGCAACAATTTC AGTCTTGCTTCTAGGGCTAGACAGGAACTTGGCAAACATCTGTGGCCTGTTCAGCAAAGGATGTTAATA TTTAAGAATCTTGTCTTGGGCTGGGTGTGGAGGCAAGTGGATCACAGGAGGTCAGGAGTTTGAGACCAA CCTGGCCAACATGATGAAACCCCATCTCTACCAAAAAAAATACAAATCAGCTGGGCGTCGTGGTGTGCC TGTAGTCCCAACGCAGGAGGTTGAGGGGAGAATTGCTTGAACCCAGGAGGTGGTGGTTGCAGTGAGATT GAGCAACTGCAATCCAGCCTGGGCGACGGAGTGAGACTGTCTCAAAAAAAAAAAAAAAAGGATCGTCTC AACCTTTGCCCTCCTACTGCAACATTTTGGTATTTGAAATGAAGGGACCTTCCATACTTATGCTGTTAA TACTTTCATTCTCACTAGGGATGAAGCACATTCCTAACCTGCTTCCTAATGGGGATGCTTCGCCAGCCA GGTCCTCACCTGTGTGTACACCAGCAGGACACTGATCCAGTCACAGCCATACAGCTGTCCACACTGAAG AACATGTCCTACAACAGCCTGAATCAAATGGTTAGCTTAATAGATAAAAATCCCAGACTACTTCAGCCT TTAATGCCTTTTATTCATAAAAACTGTGAAAGCTAGACTGAACCATTGGAAACATTTAACTCAGACTCT GGATTCAGAGTCGGGAACCCTTAGTTCTATCTGAATCCAAGACAGCCACACCTTAGTATACTGCCCAAA CTAATGAGTTTAATAAATACAAATACTCGTTTCTTTTTGATTAGTGTGATTAGAACTGAACAACGGCAC TTAAGGAATCTGGAAGATAGCCTGGATAGATTTCTGATTCATCCCAAGACCTCAAAGACAACACCTGGG TACCAAATTTCTTTATTTGAAGGAATGGTACAAATCAAAGAACTTAAGTGGATGTTTTGGTACAACTTA TAGAAAAGGTAAAGGAAACCCCAACATGCATGCACTGCCTTGGTGACCAGGGAAGTCACCCCACGGCTA TGGGGAAATTAGCCCGAGGCTTAGCTTTCATTATCACTGTCTCCCAGGGTGTGCTTGTCAAAGAGATAT TCCGCCAAGCCAGATTCGGGCGCTCCCATCTTGCGCAAGTTGGTCACGTGGTCACCCAATTCTTTGATG GCTTTCACCTGCTCATTCAGGTAATGTGTCTCAATGAAGTCACACAACTGCAAAACAATGGGGAAGACA GTTAGTGGGCAGCTTTCCCAATCCCTAAGGCAAATGATTTCCTCCATTTATTTCCTGGGGTTCCAATAC TCACATGGGGGTCATTTTTGTCAGTGGCCAGTTTGTGCAGTTCCAGTAGTGACTGATTCACATTTTTTT CCAAATGTAATGCACACTCCATTGCATTCAGCCCGCTCTCCCAGTCATCACAGTCTGGTTTCTGAATG 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_001139443.2 |
Synonyms | ARB; BEST; Best1V1Delta2; BMD; RP50; TU15B; VMD2 |
Summary | This gene encodes a member of the bestrophin gene family. This small gene family is characterized by proteins with a highly conserved N-terminus with four to six transmembrane domains. Bestrophins may form chloride ion channels or may regulate voltage-gated L-type calcium-ion channels. Bestrophins are generally believed to form calcium-activated chloride-ion channels in epithelial cells but they have also been shown to be highly permeable to bicarbonate ion transport in retinal tissue. Mutations in this gene are responsible for juvenile-onset vitelliform macular dystrophy (VMD2), also known as Best macular dystrophy, in addition to adult-onset vitelliform macular dystrophy (AVMD) and other retinopathies. Alternative splicing results in multiple variants encoding distinct isoforms.[provided by RefSeq, Nov 2008] |
Locus ID | 7439 |
MW | 75.1 |
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