TRIQK (NM_001191035) Human Untagged Clone

Specifications

Product Data
Type	Human Untagged Clone
Tag	Tag Free
Synonyms	C8orf83; PRO0845; UPF0599
Vector	pCMV6-Entry
Sequence Data	Fully Sequenced ORF (showhide) >SC329422 representing NM_001191035. Blue=Insert sequence Red=Cloning site Green=Tag(s) ATGGGTAGAAAAGATGCTGCTACTATAAAACTTCCTGTTGATCAGTACAGAAAACAAATTGGTAAACAG GATTATAAAAAAACTAAACCTATTTTACGAGCAACCAAATTAAAAGCAGAAGCAAAGAAAACAGCAATA GGCATAAAGGAAGTTGGCCTTGTACTTGCAGCTATATTGGCACTACTACTGGCTTTCTATGCTTTCTTT TATCTCAGACTCACCACGGATGTTGACCCTGATCTGGACCAAGATGAAGATTAG
Restriction Sites	SgfI-MluI
ACCN	NM_001191035
Insert Size	261 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_001191035.1
RefSeq Size	3779 bp
RefSeq ORF	261 bp
Locus ID	286144
UniProt ID	Q629K1
MW	9.7 kDa
Gene Summary	May play a role in cell growth and maintenance of cell morphology.[UniProtKB/Swiss-Prot Function] Transcript Variant: This variant (6) differs in the 5' UTR, compared to variant 1. Variants 1-7 all encode the same protein. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.

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