PRAME (NM_206953) Human 3' UTR Clone
CAT#: SC205140
3' UTR clone of preferentially expressed antigen in melanoma (PRAME) 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
![](https://cdn.origene.com/img/defaults-img.jpg)
经常一起买 (2)
Specifications
Product Data | |
Product Name | PRAME (NM_206953) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CT130; MAPE; OIP-4; OIP4 |
ACCN | NM_206953 |
Insert Size | 396 bp |
Sequence Data |
>SC205140 3’UTR clone of NM_206953
The sequence shown below is from the reference sequence of NM_206953. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATCCTGTGCCCCTGTTTCATGCCTAATTAGCTGGGTGCACATATCAAATGCTTCATTCTGCATACTTGG ACACTAAAGCCAGGATGTGCATGCATCTTGAAGCAACAAAGCAGCCACAGTTTCAGACAAATGTTCAGT GTGAGTGAGGAAAACATGTTCAGTGAGGAAAAAACATTCAGACAAATGTTCAGTGAGGAAAAAAAGGGG AAGTTGGGGGTAGGCAGATGTTGACTTGAGGAGTTAATGTGATCTTTGGGGAGATACATCTTATAGAGT TAGAAATAGAATCTGAATTTCTAAAGGGAGATTCTGGCTTGGGAAGTACATGTAGGAGTTAATCCCTGT GTAGACTGTTGTAAAGAAACTGTTGAAAATAAAGAGAAGCAATGTGAAGCA 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_206953.3 |
Synonyms | CT130; MAPE; OIP-4; OIP4 |
Summary | This gene encodes an antigen that is preferentially expressed in human melanomas and that is recognized by cytolytic T lymphocytes. It is not expressed in normal tissues, except testis. The encoded protein acts as a repressor of retinoic acid receptor, and likely confers a growth advantage to cancer cells via this function. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014] |
Locus ID | 23532 |
MW | 15.2 |
Documents
Product Manuals |
FAQs |
Resources
Customer
Reviews
Loading...