DHCR7 (NM_001360) Human Untagged Clone

CAT#: SC110871

DHCR7 (untagged)-Human 7-dehydrocholesterol reductase (DHCR7), transcript variant 1



  "NM_001360" in other vectors (6)

CNY 2,950.00


货期*
现货

规格
    • 10 ug

Cited in 1 publication.

Product images

经常一起买 (4)
Rabbit Polyclonal Anti-DHCR7 Antibody
    • 100 ul

CNY 1,999.00
CNY 3,280.00


TurboFectin Transfection Reagent (1 mL in 1 vial)
    • 1 ml in 1 vial

CNY 4,090.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1,280.00


Forward sequencing primer VP1.5, Reverse sequencing primer XL39, 100pmoles each
    • 100 pmol

CNY 480.00

Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Synonyms SLOS
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC110871 sequence for NM_001360 edited (data generated by NextGen Sequencing)
ATGGCTGCAAAATCGCAACCCAACATTCCCAAAGCCAAGAGTCTAGATGGCGTCACCAAT
GACAGAACCGCATCTCAAGGGCAGTGGGGCCGTGCCTGGGAGGTGGACTGGTTTTCACTG
GCGAGCGTCATCTTCCTACTGCTGTTCGCCCCCTTCATCGTCTACTACTTCATCATGGCT
TGTGACCAGTACAGCTGCGCCCTGACTGGCCCTGTGGTGGACATCGTCACCGGACATGCT
CGGCTCTCGGACATCTGGGCCAAGACTCCACCTATAACGAGGAAAGCCGCCCAGCTCTAT
ACCTTGTGGGTCACCTTCCAGGTGCTTCTGTACACGTCTCTCCCTGACTTCTGCCATAAG
TTTCTACCCGGCTACGTAGGAGGCATCCAGGAGGGGGCCGTGACTCCTGCAGGGGTTGTG
AACAAGTATCAGATCAATGGCCTGCAAGCCTGGCTCCTCACGCACCTGCTCTGGTTTGCA
AACGCTCATCTCCTGTCCTGGTTCTCGCCCACCATCATCTTCGACAACTGGATCCCACTG
CTGTGGTGCGCCAACATCCTTGGCTATGCCGTCTCCACCTTCGCCATGGTCAAGGGCTAC
TTCTTCCCCACCAGCGCCAGAGACTGCAAATTCACAGGCAATTTCTTTTACAACTACATG
ATGGGCATCGAGTTTAACCCTCGGATCGGGAAGTGGTTTGACTTCAAGCTGTTCTTCAAT
GGGCGCCCCGGGATCGTCGCCTGGACCCTCATCAACCTGTCCTTCGCAGCGAAGCAGCGG
GAGCTCCACAGCCATGTGACCAATGCCATGGTCCTGGTCAACGTCCTGCAGGCCATCTAC
GTGATTGACTTCTTCTGGAACGAAACCTGGTACCTGAAGACCATTGACATCTGCCATGAC
CACTTCGGGTGGTACCTGGGCTGGGGCGACTGTGTCTGGCTGCCTTATCTTTACACGCTG
CAGGGTCTGTACTTGGTGTACCACCCCGTGCAGCTGTCCACCCCGCACGCCGTGGGCGTC
CTGCTGCTGGGCCTGGTGGGCTACTACATCTTCCGGGTGGCCAACCACCAGAAGGACCTG
TTCCGCCGCACGGATGGGCGCTGCCTCATCTGGGGCAGGAAGCCCAAGGTCATCGAGTGC
TCCTACACATCCGCCGATGGGCAGAGGCACCACAGCAAGCTGCTGGTGTCGGGCTTCTGG
GGCGTGGCCCGCCACTTCAACTACGTCGGCGACCTGATGGGCAGCCTGGCCTACTGCCTG
GCCTGTGGCGGCGGCCACCTGCTGCCCTACTTCTACATCATCTACATGGCCATCCTGCTG
ACCCACCGCTGCCTCCGGGACGAGCACCGCTGCGCCAGCAAGTACGGCCGGGACTGGGAG
CGCTACACCGCCGCAGTGCCTTACCGCCTGCTGCCTGGAATCTTCTAA

Clone variation with respect to NM_001360.2
>OriGene 5' read for NM_001360 unedited
NGGGCAAAATTTGTATACGACTCATATAGGGCGGCCGCGATTCGGCACGAGCCTCGTGCC
GAATTCGGCACGAGGGTGGAGCAGCGCGCGCAAGCGAGGCCAGGGGAAGGTGGGCGCAGG
TGAGGGGCCGAGGTGTGCGCAGGACTTTAGCCGGTTGAGAAGGATCAAGCAGGCATTTGG
AGCACAGGTGTCTAGAAACTTTTAAGGGGCCGGTTCAAGAAGGAAAAGTTCCCTTCTGCT
GTGAAACTATTTGGCAAGAGGCTGGAGGGCCCAATGGCTGCAAAATCGCAACCCAACATT
CCCAAAGCCAAGAGTCTAGATGGCGTCACCAATGACAGAACCGCATCTCAAGGGCAGTGG
GGCCGTGCCTGGGAGGTGGACTGGTTTTCACTGGCGAGCGTCATCTTCCTACTGCTGTTC
GCCCCCTTCATCGTCTACTACTTCATCATGGCTTGTGACCAGTACAGCTGCGCCCTGACT
GGCCCTGTGGTGGACATCGTCACCGGACATGCTCGGCTCTCGGACATCTGGGCCAAGACT
CCACCTATAACGAGGAAAGCCGCCCAGCTCTATACCTTGTGGGTCACCTTCCAGGTGCTT
CTGTACACGTCTCTCCCTGACTTCTGCCATAAGTTTCTACCCGGCTACGTAGGAGGCATC
CAGGAGGGGGCCGTGACTCCTGCAGGGGTTGTGAACAAGTATCAGATCAATGGCCTGCAA
GCCTGGCTCCTCACGCACCTGCTCTGGTTTGCAAACGCTCATCTCCTGTCCTGGTTCTCG
CCCACCATCATCTTCGACAACTGGATCCCACTGCTGTGTTGCGCCCACATCCTTGGCTAT
GCCGTCTCCACCTTCGNCATGGTCAAGGGCTACTTTTTTCCCACCAGGGCCAGAGACTGG
>OriGene 3' read for NM_001360 unedited
GGCACGCAATCTAGAGTCGAGTTTTTTTTTTTTTTTTTTTTTCTTTTTTTCTTTTTTCTT
TTTTTTCTTTTTTTCTTTTTTTTTCTTGAACAGGGGGAAATTTAATTTAAAAATGAACTC
TTCTCGGAGCCTAAAGTTTAAAAAAAGTTTTACCCAACCCCCTTGGGGTGAGGAAAAATG
CCCCAGGGGAAAAAAGCCCAAAAAAGGGGGGGCCCTCCCGAGGGTGGGACTGAAACCTCC
TCCCTGGAAAAAGGGGGGGAGGCCCCTGAGGGGGAATTTCCCCGGGTTGGTTGAGCCAAA
TTTTGCCCAGTCTTTGGGCAAGCAAAAAATTTTTTCGAAAGGGGGGGCGCTCCCAGGGAA
TTGGGAAACAAAACCCCCCTGCCTTCCCCTGAAAGGGCCCAGCCGGGGCTGGGACCTTTT
TTAGGGCTGCAAATTCCAGGCAAAACACTCCTGGCAGCTGTGCCCCAGGATCCCGAAGGA
AACCACCTGAAAGCCCCTTTTTTCCCATGGTCCCAGTTTAACACCGGGCCCCCTCCCAAG
GGAAAAACGGGCACGGGCCCCCCCCACCATTGTATAATTCGCACGCGAGGGGGTTTCTTA
TCTCGTAGGCCCTTCCTGGATTCCCCCCCGCCCCCCTCTCCCTTTTTTTTACCACTGATT
AATTGCCTCTATTGAAAGGGCGTGGGAAACCCCTCTGTTCCCCATTGGGCCTAACTGATC
CTGTCTCCGTCTCCTAAACGGCAATTTTCTTCCCAGGACTTCTTTAGGTCCCTGTGTTAT
CCTTTGCCCCCAGATTCCGTTTTTAAATTTACTCTTTGTCGGTACTCCCCATTTCCTCCA
CCTCCGTCTCCTTATTGCATTACTTTCTAAAACTCCTTTTCATCTTCACTCTTCACTATG
CCCACTTTCTCTCCTCATACCCCATCTTGTCTCCCCGCTGACCTTATTCTCCTTATCTTG
TTTATCCGTGCT
Restriction Sites NotI-NotI     
ACCN NM_001360
Insert Size 2800 bp
OTI Disclaimer Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Product Components The ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water).
Reconstitution 1. Centrifuge at 5,000xg for 5min.
2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA.
3. Close the tube and incubate for 10 minutes at room temperature.
4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom.
5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C.
Reference Data
RefSeq NM_001360.1, NP_001351.1
RefSeq Size 2597 bp
RefSeq ORF 1428 bp
Locus ID 1717
UniProt ID Q9UBM7
Domains ERG4_ERG24
Protein Families Druggable Genome, Transmembrane
Protein Pathways Metabolic pathways, Steroid biosynthesis
Gene Summary This gene encodes an enzyme that removes the C(7-8) double bond in the B ring of sterols and catalyzes the conversion of 7-dehydrocholesterol to cholesterol. This gene is ubiquitously expressed and its transmembrane protein localizes to the endoplasmic reticulum membrane and nuclear outer membrane. Mutations in this gene cause Smith-Lemli-Opitz syndrome (SLOS); a syndrome that is metabolically characterized by reduced serum cholesterol levels and elevated serum 7-dehydrocholesterol levels and phenotypically characterized by cognitive disability, facial dysmorphism, syndactyly of second and third toes, and holoprosencephaly in severe cases to minimal physical abnormalities and near-normal intelligence in mild cases. Alternative splicing results in multiple transcript variants that encode the same protein.[provided by RefSeq, Aug 2009]
Transcript Variant: This variant (1) represents the longer transcript. Variants 1 and 2 encode the same protein.
*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.

Citations (1)

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