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
Need custom modification / cloning service?
Get a free quote
CNY 4,845.00
货期*
3周
规格
Product images
经常一起买 (2)
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 |
Documents
Product Manuals |
FAQs |
Resources
Customer
Reviews
Loading...