NSDHL (NM_015922) Human 3' UTR Clone
CAT#: SC203332
3' UTR clone of NAD(P) dependent steroid dehydrogenase-like (NSDHL) transcript variant 1 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 | NSDHL (NM_015922) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | H105E3; SDR31E1; XAP104 |
ACCN | NM_015922 |
Insert Size | 643 bp |
Sequence Data |
>SC203332 3’UTR clone of NM_015922
The sequence shown below is from the reference sequence of NM_015922. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AGCTTTCGCCACCTGCGGAGGGTCAAGTGAGGGACACTGGAGGCTGGGCTCTCTCGACACGTTGCTCAG CCAGTCACTCCTTCCCCTGTGGATTGATGAAATAACATCCTTTGAATGAGTTTGCTCTGAGCCTGTGAC TCCTTCTGCTAGGCAGAGAGCGCACCCTACTCTTTCCGTGACGATGAGGGCGGCAAAAACAGACATTTC TTCCTTCATGGAACTGGATTTGGATTTCTTGAAGCAGGCAGCTTCATATTATACCGATTTGTTCTCTGT CTTTTTGTGTCTCTCTGTTTACCCCCTCCCTTGCCCCCTCTTCTGGTTTATACATTTCATTCCAGTGTC CTTGTACATAATCAAGGAAGCTGTAGGAAGCTACAACCCATTTGTTAGTTCTGATGGAGAACCATTTCC ATGCAGACCAATACTAGAGTGAAGCCTCTAGACTTTGTTCAAGATACTCTATCTTCAAAATATCCCAGA AGAAAAACAGAAGCTGTTAACACACAGGTGAGACTTTACATATACATTTCATACTGACAGTGAGCTTAG AGCAAAAGCTGAAAGCTGAAATGACTGTAATTCCTCCCCAGTCTCTGTTGCTTGTTCAACTCCTTACAT GTTCCACATTCTCTTTCAGGTA 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_015922.3 |
Synonyms | H105E3; SDR31E1; XAP104 |
Summary | The protein encoded by this gene is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene. [provided by RefSeq, Jul 2008] |
Locus ID | 50814 |
MW | 24.3 |
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