ATP2C1 (NM_001001487) Human 3' UTR Clone

CAT#: SC206552

3' UTR clone of ATPase Ca++ transporting type 2C member 1 (ATP2C1) 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 ATP2C1 (NM_001001487) Human 3' UTR Clone
Vector pMirTarget
Synonyms ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1
ACCN NM_001001487
Insert Size 495 bp
Sequence Data
>SC206552 3’UTR clone of NM_001001487
The sequence shown below is from the reference sequence of NM_001001487. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
CCACTGACAGAAGATGTGAGCTGTGTCTAAGTCCAGTCTTGTGCCCAGCCGTGTCTGCGCCTTCACTCT
TTGGAACTCTGCATACAACATCTTAGCACCATCTTCCTGCAGCTCTTCCTTACCTAAATAAAGAAACAG
CCCAAGGGCAGTATTTCTAAAAGCACTGTAACAGCTTTTCATTTTCTCCACATATACTACAAATTCTAT
AAAGAAAGAAATTAATTTAAAAAAACTAAGATGTTTTTCTCTTCTGGCTTCATAAATGCCTTGCTGTAT
AAATTGAAATATTGATACTGAACTGTCTTTTTAATGATGACCTAACTTTATTCAACCCATCGGAATTTA
CTTTTTCCCTGAAATAAGATCTTTTCCACTGGTCTACTACCTGACCATAAACATGTCTGCATTTGAATT
CTCTAAACCCTAAATCTGTGTCTATGAAAAATACAAATGACTATTAAATATTATTCTCTTTACTGTTCT
CTTTCACCGAAA
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_001001487.2
Synonyms ATP2C1A; BCPM; HHD; hSPCA1; PMR1; SPCA1
Summary The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of calcium ions. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011]
Locus ID 27032
MW 19.4
*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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