TRPM7 (NM_017672) Human 3' UTR Clone

CAT#: SC214341

3' UTR clone of transient receptor potential cation channel subfamily M member 7 (TRPM7) 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 TRPM7 (NM_017672) Human 3' UTR Clone
Vector pMirTarget
Synonyms ALSPDC; CHAK; CHAK1; LTrpC-7; LTRPC7; TRP-PLIK
ACCN NM_017672
Insert Size 2000 bp
Sequence Data
>SC214341 3’UTR clone of NM_017672
The sequence shown below is from the reference sequence of NM_017672. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
TCAACTAATTCTGTTCGTCTGATGTTATAATATTAATATTACTGAATCATTGGTTTTGCCTGCACCTCA
CAGAAATGTTACTGTGTCACTTTTCCCTCGGGAGGAAATTGTTTGGTAATATAGAAAGGTGTATGCAAG
TTGAATTTGCTGACTCCAGCACAGTTAAAAGGTCAATATTCTTTTGACCTGATTAATCAGTCAGAAAGT
CCCTATAGGATAGAGCTGGCAGCTGAGAAATTTTAAAGGTAATTGATAATTAGTATTTATAACTTTTTA
AAGGGCTCTTTGTATAGCAGAGGATCTCATTTGACTTTGTTTTGATGAGGGTGATGCTCTCTCTTATGT
GGTACAATACCATTAACCAAAGGTAGGTGTCCATGCAGATTTTATTGGCAGCTGTTTTATTGCCATTCA
ACTAGGGAAATGAAGAAATCACGCAGCCTTTTGGTTAAATGGCAGTCAAAATTTTCCTCAGTGTATTTA
GTGTGTTCAGTGATGATATCACTGGTTCCCAACTAGATGCTTGTTGGCCACGGGAAGGGAAATGACTTG
TTCTAATTCTAGGTTCACAGAGGTATGAGAAGCCTGAACTGAAGACCATTTTCAAGAGGGACGGTATTT
ATGAATCAGGGTTAGGCTCCATATTTAAAGATAGAGCCAGTTTTTTTTTTTAAATAGAACCCAAATTGT
GTAAAAATGTTAATTGGGTTTTTTAAACATTGTTTTATCAAGTCACTGTTAAGTAGAAGAAAGCCATGG
TAAACTGATACATAACCTAAATTATAAAAGCAGAAACCTAACTCACTCGTCAAGGGAAGTTACCTTTTG
AGGAAAGTTAAAGTACTTTTTTCCCTATCTGTATCTATAGCAACAACCCAGAACTTACAAACTTCTCCA
AAGATTTTATTGATTGTTATATCAAATCAGAATGTAAACATGAACTCTTGCATATATTTAAAATTGTGT
TGGAACATTTGAACATGAATGCTGTTTGTGGTACTTAAGAAATTAATTCAGTTGGATTATCATTATGTG
ATACTGGCAGATTGCAGTGCAACCTTATGCCAATAAAATGTAATTTAACAGCCCCAGATATTGTTGAAT
ATTCAACAATAACAAGAAAAGCTTTTCATCTAAGTTTTATGCTTTAATTTTTTTTCTTTTTTTTTCTTT
TTCTTTTGTTTCCTTGGTACTAATTTTAATTTTTATTTGGAAGGGAGCAGTATAAAGCTTATTTGTATT
TAGTAGTGTATCTCATAGATACAGACAAGGCAAGAGATGATAAGCTGTTTAAATAGTGTTTAATATTGA
TTGGGGGTGGGGAGAAAGAAAAAGTGTATTACTTAAAGATACTATATACGTTTTGTATATCATTAAATC
TTTAAAAGAAATGAAATAAATTTATTGTTTACAGATGTTTAGTGAGTTTAATCATTCTGAAAAATTATC
TGACATTTTCAGGGTGTCAATTTGAGTATCAGTTTTTTTAAATGAACCATTTGTATACCTGTGCTTTTG
ATCTCCTGTCCTGTACAATGTTTAAATTAATACTGATTTCTTACTGTCTTCTTAGAAATCTGTTTTTTG
TTAGGCCAAAAAAGGGCAATATGGGCTGTCTGTTGATTTTTAATTTTATATTGATTATTTTCACAGGAT
TATAATAGTAGCTATACTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTTGCTTGGGCT
GGAGTGCAGTGGTGCGATCTCAGCTCACCACAACCGCCGCCTTCCGGGTTTAAGTGATTCTCCTGCCTC
AGCCTCCCGAGTAGCTGGGACTACAGGCACACGCCACCATGCCCAGCTAATTTTTATATTTTTAGTAGA
GACAGGGTTTCACTATGTTGGCCAGTGTGGTCACAAACTCCTGACCTTGTGAGCCACCGCACCTGGCTG
CTAACACTTATTTAGTGCCTACTGTGTACCAGACATTACTCTAAGTATTTCACATATATTAACCTACT
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_017672.6
Synonyms ALSPDC; CHAK; CHAK1; LTrpC-7; LTRPC7; TRP-PLIK
Summary This gene belongs to the melastatin subfamily of transient receptor potential family of ion channels. The protein encoded by this gene is both an ion channel and a serine/threonine protein kinase. The kinase activity is essential for the ion channel function, which serves to increase intracellular calcium levels and to help regulate magnesium ion homeostasis. The encoded protein is involved in cytoskeletal organization, cell adhesion, cell migration and organogenesis. Defects in this gene are a cause of amyotrophic lateral sclerosis-parkinsonism/dementia complex of Guam. The gene may also be associated with defects of cardiac function. [provided by RefSeq, Aug 2017]
Locus ID 54822
MW 77.5
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