NR2E3 (NM_016346) Human Untagged Clone

CAT#: SC114329

NR2E3 (untagged)-Human nuclear receptor subfamily 2, group E, member 3 (NR2E3), transcript variant 1



  "NM_016346" in other vectors (6)

CNY 3,656.00

CNY 5,990.00


货期*
现货

规格
    • 10 ug

Product images

经常一起买 (4)
NR2E3 mouse monoclonal antibody, clone OTI3D4 (formerly 3D4)
    • 100 ul

CNY 1,999.00
CNY 2,700.00


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 ESCS; PNR; rd7; RNR; RP37
Vector pCMV6-XL4
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC114329 sequence for NM_016346 edited (data generated by NextGen Sequencing)
ATGGAGACCAGACCAACAGCTCTGATGAGCTCCACAGTGGCTGCAGCTGCGCCTGCAGCT
GGGGCTGCCTCCAGGAAGGAGTCTCCAGGCAGATGGGGCCTGGGGGAGGATCCCACAGGC
GTGAGCCCCTCGCTCCAGTGCCGCGTGTGCGGAGACAGCAGCAGCGGGAAGCACTATGGC
ATCTATGCCTGCAACGGCTGCAGCGGCTTCTTCAAGAGGAGCGTACGGCGGAGGCTCATC
TACAGGTGCCAGGTGGGGGCAGGGATGTGYCCCGTGGACAAGGCCCACCGCAACCAGTGC
CAGGCCTGCCGGCTGAAGAAGTGCCTGCAGGCGGGGATGAACCAGGACGCCGTGCAGAAC
RAGCGCCAGCCGCGAAGCACAGCCCAGGTCCACCTGGACAGCATGGAGTCCAACACTGAN
NNNNNNNNNGAGTCCCTGGTGGCTCCCCCGGCCCCGGCAGGGCGCAGCCCACGGGGCCCC
ACACCCATGTCTGCAGCCAGAGCCCTGGGCCACCWCTTCATGGCCAGCCTTATAACAGCT
GAAACCTGTGCTAAGCTGGAGCCAGAGGATGCTGATGAGAATATTGATGTCACCAGCAAT
GACCCTGAGTTCCCCTCCTCTCCATACTCCTCTTCCTCCCCCTGCGGCCTGGACAGCATC
CATGAGACCTCGGCTCGCCTACTCTTCNNNNNNNNCAAGTGGGCCAAGAACCTGCCTGTG
TTCTCCAGCCTGCCCTTCCGGGATCAGGTGATCCTGCTGGAAGAGGCGTGGAGTGAACTC
TTTCTCCTCGGGGCCATCCAGTGGTCTCTGCCTCTGGACAGCTGTCCTCTGCTGGCACCG
CCCGAGGCCTCTGCTGCCGGTGGTGCCCAGGGCCGGCTCACGCTGGCCAGCATGGAGACG
CGTGTCCTGCAGGAAACTATCTCTCGGTTCCGGGCATTGGCGGTGGACCCCACGGAGTTT
GCCTGCATGAAGGCCTTGGTCCTCTTCAAGCCAGAGACGCGGGGCCTGAAGGATCCTGAG
CACGTAGAGGCCTTGCAGGACCAGTCCCAAGTGATGCTGAGCCGGCACAGCAAGGCCCAC
CACCCCAGCCAGCCCGTGAGGTGA

Clone variation with respect to NM_016346.2
270 c=>y;361 g=>r;420 g=>n;421 t=>n;422 c=>n;423 c=>n;424 c=>n;425 g=>n;426 g=>n;427 c=>n;428 c=>n;429 g=>n;515 a=>w;688 a=>n;689 t=>n;690 g=>n;691 g=>n;692 c=>n;693 c=>n;694 g=>n;695 t=>n;1064 a=>g
>OriGene 5' read for NM_016346 unedited
TCATAATTGTAAACGACTCATATAGGCGGCCGCGCAATCANATCTGGTACCGAGCTCGGC
TCCACTAGTAACGGCCGCCAGTGTGCTGGAATTCGCCCTTGCCCTGTAACCCATGGAGAC
CAGACCAACAGCTCTGATGAGCTCCACAGTGGCTGCAGCTGCGCCTGCAGCTGGGGCTGC
CTCCAGGAAGGAGTCTCCAGGCAGATGGGGCCTGGGGGAGGATCCCACAGGCGTGAGCCC
CTCGCTCCAGTGCCGCGTGTGCGGAGACAGCAGCAGCGGGAAGCACTATGGCATCTATGC
CTGCAACGGCTGCAGCGGCTTCTTCAAGAGGAGCGTACGGCGGAGGCTCATCTACAGGTG
CCAGGTGGGGGCAGGGATGTGTCCCGTGGACAAGGCCCACCGCAACCAGTGCCAGGCCTG
CCGGCTGAAGAAGTGCCTGCAGGCGGGGATGAACCAGGACGCCGTGCAGAACAAGCGCCA
GCCGCGAAGCACAGCCCAGGTCCACCTGGACAGCATGGAGTCCAACACTGAGTCCCGGCC
GGAGTCCCTGGTGGCTCCCCCGGCCCCGGCAGGGCGCAGCCCACGGGGCCCCACACCCAT
GTCTGCAGCCAGAGCCCTGGGCCACCTCTTCATGGCCAGCCTTATAACAGCTGAAACCTG
TGCTAAGCTGGAGCCAGAGGATGCTGATGAGAATATTGATGTCACCAGCAATGACCCTGA
GTTCCCCTCCTCTCCATACTCCTCTTCCTCCCCCTGCGGCCTGGACAGCATCCATGAGAC
CTCGGCTCGCCTACTCTTCATGGCCGTCAAGTGGGCCAAGAACCTGCCTGTGNTCTCCAG
CCTGCCATTNCGGGATCAGGTATCTACCGGCCTGCCTGCTGNGGAGCTAGGCTGGGNNCT
GAGTCANGGCGCCCACTCNAGTCACCAGACAGGCACACACATCCCCACGCAGTATGATGC
ACACGCTTGGATGGTGATGGCTGGGGCACACATACTCTGATC
>OriGene 3' read for NM_016346 unedited
GNGANAGCACTGGGGNAGGGTCACAGGNATGCCACCCGGGATCTGTTCAGGAACAGCTAT
GACCGCGGCCGCCAGTGTGATGGATATCTGCAGAATTCGCCCTTCTGGGAGAGTGTGGGA
GAGGCAGAGAAAGGTTAGAGGTCAGGGACAGATGAGTGGGTGGGCGCATGCTCAGGTCAC
CTCACGGGCTGGCTGGGGTGGTGGGCCTTGCTGTGCCGGCTCAGCATCACTTGGGACTGG
TCCTGCAAGGCCTCTACGTGCTCAGGATCCTTCAGGCCCCGCGTCTCTGGCTTGAAGAGG
ACCAAGGCCTTCATGCAGGCAAACTCCGTGGGGTCCACCGCCAATGCCCGGAACCGAGAG
ATAGTTTCCTGCAGGACACGCGTCTCCATGCTGGCCAGCGTGAGCCGGCCCTGGGCACCA
CCGGCAGCAGAGGCCTCGGGCGGTGCCAGCAGAGGACAGCTGTCCAGAGGCAGAGACCAC
TGGATGGCCCCGAGGAGAAAGAGTTCACTCCACGCCTCTTCCAGCAGGATCACCTGTGCT
NCAGACAGGGGTGCCTGTTATGGCAGACACACAGCTTCTCTGGCTCAGTCTGGAGCCTCT
GCCACCATCTCAGGCACCCAAGGAATGGGGAAGTGCTGTCCTGAGACCCGAGAATGCTCT
CCTGACATCAGCCAGAGGCTCAGAGCTCTGGNGATTTGGCACCATCCGGCTCAGCTGCCT
ATCATCTGAGACAACTGGGTTCCATCCAGAGCTGCAGCTGGGACATTNTANGAACGCCAG
NACATTGGGGAGTTGGGCAGCCTCAGAGACTGCTCATGAGTGCCTAAGTTGATGTATTCA
AGGGGTGGGGCTGACTCTTCTGAGTGCT
Restriction Sites Please inquire     
ACCN NM_016346
Insert Size 2300 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.
Note Plasmids are not sterile.  For experiments where strict sterility is required, filtration with 0.22um filter is required.
Reference Data
RefSeq NM_016346.2, NP_057430.1
RefSeq Size 2102 bp
RefSeq ORF 1104 bp
Locus ID 10002
UniProt ID Q9Y5X4
Protein Families Druggable Genome, Nuclear Hormone Receptor, Transcription Factors
Gene Summary This protein is part of a large family of nuclear receptor transcription factors involved in signaling pathways. Nuclear receptors have been shown to regulate pathways involved in embryonic development, as well as in maintenance of proper cell function in adults. Members of this family are characterized by discrete domains that function in DNA and ligand binding. This gene encodes a retinal nuclear receptor that is a ligand-dependent transcription factor. Defects in this gene are a cause of enhanced S cone syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Transcript Variant: This variant (1) represents the longer transcript and encodes isoform a.
*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.

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