DPM1 (NM_003859) Human 3' UTR Clone
CAT#: SC203320
3' UTR clone of dolichyl-phosphate mannosyltransferase polypeptide 1 catalytic subunit (DPM1) for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | DPM1 (NM_003859) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CDGIE; MPDS |
ACCN | NM_003859 |
Insert Size | 292 bp |
Sequence Data |
>SC203320 3’UTR clone of NM_003859
The sequence shown below is from the reference sequence of NM_003859. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GGATTATTGACTCTTTTTGCTACTACATAAAAGAAAGATACTCATTTATAGTTACGTTCATTTCAGGTT AAACATGAAAGAAGCCTGGTTACTGATTTGTATAAAATGTACTCTTAAAGTATAAAATATAAGGTAAGG TAAATTTCATGCATCTTTTTATGAAGACCACCTATTTTATATTTCAAATTAAATAATTTTAAAGTTGCT GGCCTAATGAGCAATGTTCTCAATTTTCGTTTTCATTTTGCTGTATTGAGACCTATAAATAAATGTATA TTTTTTTTTGCATAAA 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_003859.3 |
Synonyms | CDGIE; MPDS |
Summary | Dolichol-phosphate mannose (Dol-P-Man) serves as a donor of mannosyl residues on the lumenal side of the endoplasmic reticulum (ER). Lack of Dol-P-Man results in defective surface expression of GPI-anchored proteins. Dol-P-Man is synthesized from GDP-mannose and dolichol-phosphate on the cytosolic side of the ER by the enzyme dolichyl-phosphate mannosyltransferase. Human DPM1 lacks a carboxy-terminal transmembrane domain and signal sequence and is regulated by DPM2. Mutations in this gene are associated with congenital disorder of glycosylation type Ie. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015] |
Locus ID | 8813 |
MW | 11.4 |
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