GLRB (NM_001166061) Human 3' UTR Clone

CAT#: SC215897

3' UTR clone of glycine receptor beta (GLRB) transcript variant 3 for miRNA target validation



Need custom modification / cloning service?
Get a free quote

CNY 6,504.00


货期*
现货

规格
    • 10 ug

Cited in 1 publication.

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 GLRB (NM_001166061) Human 3' UTR Clone
Vector pMirTarget
Synonyms HKPX2
ACCN NM_001166061
Insert Size 1681 bp
Sequence Data
>SC215897 3’UTR clone of NM_001166061
The sequence shown below is from the reference sequence of NM_001166061. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
AGTGCTGCCAGAGTGCCCCTGGGTTGGTGAGACCAGATGCAAAAAAGTTTGTACTTCTAAGTCTGATCT
GAGATCTAATGACTTCAGCATTGTTGGAAGCTTACCAAGAGATTTTGAACTATCCAATTATGACTGCTA
TGGAAAACCCATTGAAGTTAACAACGGACTTGGGAAATCTCAGGCTAAGAACAACAAGAAGCCTCCCCC
TGCGAAACCTGTTATTCCAACAGCAGCAAAGCGAATTGATCTTTATGCAAGAGCATTGTTTCCTTTCTG
CTTCTTGTTCTTCAATGTTATATATTGGTCTATATATTTATGATAAATCTTTTCCATTTGTACAAAATA
AAATTCCATTTCATTGTGACCTACTCCTTTCATAAATGCCAATCTGTGAGAACTTTTGAATTTTCATAG
CAACATTGCATTTTGGATGCCATTTGATTGTAATAAAACTGTGGCACCTTAATTTTGAATGGCAGCATG
ATCATGTAATATCTGTGCTCTAATAACGATGTATATATGTATAGTGAACATATTGCTTAGTAACAAATG
AAGGACAAGCATACTACATAATATAATCCATACAATTCTCTTCAGTTAGTGTAAACTGCAAATACTACA
GATAATTCTGATAATAAAATGATATGCACGCTGAATCCTGCTATGGTCACCATTCTAATGTATGTAGTA
TTTCAAATTTCCTTCCTTGTAACTTTCAAAGAAAGCCATCTTATTCTTGTAAAATTTTAGATGGTATTA
TCACAGATTTAAAAAGGTTGTATTACATATTGTTTAAACTTTGTAAGTAGAAATATATCTGTTATAATT
ATACAGGCTCTGTGGAGAAATAAAGTTCAAAATATATTAATTTGTAAAATCAGCTCGTTTTAAAGTGTG
CTTGTGTTGTCAAAAATATCAGATAGTAATACACAGTGAGCATTTTTAAACAAAGGGAAACCTATATTT
ATGTAACTGTATACTGAATTCTGACAAAATAAAAAAAGATACCTTATTGACGAAATATTTAGGATAAAC
AAAATTCTATTTAATCCACCTTAAAACCTAAATGTATTTTCATGGATTTCATTTGTTGGTACATATTAC
ACAAAACATTGTGCCTTAAAATGAGTCATACATCTTTTAAATTGGAATGCAGTAATAGATATGTGATTT
TACATCATTTTTAAGAAACCAAGGGGAAGTAATAAGTTGAAAAAGAAATCCATAACTATTAAAAGATTT
TAACTTTTTTATTTTATTAAAATGCTTGCATATTTTAAGTAAAATTAAAAATGTTTACTGAATTTATTT
TTTTATTTGAATATTTTGGGATTAGTTACAAAATATTTAGAGATTAAATAAATAATAGCTTTGTTTGTG
TTAGACTTCACTTCTACTTGTATTTTCTTTCTTGTTAAAAGTCTAGACAACTGAGATTTACTTACTTTG
AACTTGTTCCAATCCAAAAGTAAGCACTAAGTCTCATTTTATGAGACCACCATTTCTTAATATCACATC
CAGTGCACCTTTGTCTTTCTGCCATATCTGAAATAAAACTATCAGTAATTCACATAGATAAACATAAGA
CTAAAGAAGTATATTTACATTATCTGGAGAGTTTTGTTGCAGCTACGAGTTTGTATGGCAAATTCAATA
ATAAAGTATTGTTTATGCAAATTGC
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_001166061.2
Synonyms HKPX2
Summary This gene encodes the beta subunit of the glycine receptor, which is a pentamer composed of alpha and beta subunits. The receptor functions as a neurotransmitter-gated ion channel, which produces hyperpolarization via increased chloride conductance due to the binding of glycine to the receptor. Mutations in this gene cause startle disease, also known as hereditary hyperekplexia or congenital stiff-person syndrome, a disease characterized by muscular rigidity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
Locus ID 2743
MW 66
*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.

Citations (1)

Documents

Customer Reviews 
Loading...