Scfd2 (NM_001286437) Mouse Untagged Clone

Specifications

Product Data
Type	Mouse Untagged Clone
Tag	Tag Free
Synonyms	E430013M20Rik; STXBP1L1
Vector	pCMV6-Entry
E. coli Selection	Kanamycin (25 ug/mL)
Mammalian Cell Selection	Neomycin
Sequence Data	Fully Sequenced ORF (showhide) >MC228565 representing NM_001286437 Red=Cloning site Blue=ORF Orange=Stop codon TTTTGTAATACGACTCACTATAGGGCGGCCGGGAATTCGTCGACTGGATCCGGTACCGAGGAGATCTGCC GCCGCGATCGCC ATGAGCGCCGCGGGCATACTGGCCTTTGCCCAGCAAGGCTGGGAGCAGGTGCTGGCCAAAGTGAAGTGGT CCGTGGTCTACCTGGACGCTGCCTGCGCCGAGAGCCTGCACTGGAGCTGCGGATCCAGCCGGCTTCTGGA GGCGGTGAAGGGTCCTGCGTGTCACCTGCGGGAATTTGAACCCCAGGCCATTGGCGGGGGAGCCAAGCAG CCCCGGGCGGTTTTCGTTTTGAGCAGCCCGCTGAAAGGCCGGATCGTAGACACTCTACAGAGTATCATTT GCCGCAGTCACTTTCAGCACTGTGTGGTGGTCACAGCCGTGAGCCACGCAGTCCACCTCACTGCTAACCA CGTACCGGCCGCTGCAGCGGCCGAGCTCGAGGGGCAGCAGCCGGTGTTCGAACAGCTGGAGGAGAAGCTC TGTGAGTGGATGGGCAACGAGAACTATACGGCCGAGGTGCTCCACGTCCCGTTGTTTCTCGCCCCTGTTG CCTCCCATCTCGCTTTTACTCCAGCCTTTGCTACCCTCTTCCCACTGCTACCTCAGGATGTCCACGCTCT TAACAGTGCCAGACCCGACAAGAGGAGGCTGAGCAGCTTGGGTGAGGTGGATGCCACTGCCCTAACCCCA GAGCTGCTGCTGTACATCAGATGCCTCGTGTCAGGCCTCAGTTCTCTGTGTGAACATCTAGGGGTACGAG AGGAGTGTTTCGCCGTGGGTCCCCTCAGTCGGGTCATCGCTACAGATCTGGCAAATTATGCCCCCGCCAA GAACAGGAAAAAGACTGCTACAGGCAGGGCTTCTGTGGTCTTTGTGGATAGAACTCTGGATCTCACAGGA GCGGTTGGACACCACGGAGACAACTTAGTAGAGAAGATCATGTCAGTGCTTCCACAGCTTCCAGGCCACA CCCACGACGTGATGGTCAACATGGCCGAGCTCACTGCTGTCCAGGCTGTGGAGGAAAACCAGAACGTGAT TGCACCAGGCTGCCTTGCCCCATCCAATGAGGCCTCAGCCAAGGCCCTGTGGGAAGCCTTACTGAACTCC AAGCACAAAGAGGCAGTGATGGAAGTTCGGAGACATCTAGTGGAAGCAGCCAGCAGAGAGAACCTGCCCA TCAAGATGAGTATGGGAAGAGTCACTCCAGGGCAGCTCATGTCCTATATTCAACTCTTCAAGAACAACCT CAGAGCTCTTAGAAATCACTGTGGGCTTCTACAGCTTGGGATGGCCACAGTTCAAACTCTGAAGCACCCA CAGACTGCCAAGTGGGATAACTTCCTGGCATTTGAAAGGCTCCTTCTACAGAGCCTTGGGGATTCAACCA TGGCTGGTGTGCTAAATCAGCTGCTGCCAATGATTAAGTCCTCAAGCCAGAGAACCAGTGACGACCTCAA CCCTGAGGAACTGCTGATCCTGCTCATATACATTTACTCTGTCCCTGGAGACGTCACGCTGGACAGAGAC CTGGGAGACGTGGAAGAAAAGGTGAAGAAAGCATTGGCCCATGTCCTCTCTGAGGAGTCTGAGCTGTCCC CTTTGCTGCAGAAAATCACAGGCTGTGACTCTGCAGTTGACCTGACGTTGCCCAAATCCCAAATTGCTGT GAATGATGTCTTCATGGCTCTCCGGGAGATCGCTGGAGCTAGGAATCTCATGAGACAGTTTAAGTCTGTG TATGTTCCTGGAAATAACACCCATCAGGCATCCTATAAGCCGCTGTTGAAGCAGGTTGTGGAGGAAATAT TTAATCCTGAGAAGTCAGATCCTATTGACATTGAACATATGTCCTCAGGCCTCACTGATCTCCTGAAAAC TGGATTCAGCATGTTCATGAAGGTGATGGTGCTGTCCACAAGACTCCTGAAGCCGCTTAACATTCCCGAG CTGCTCTTTGCAACTGACCGGCTACACCCAGACCTCGGCTTCTGA ACGCGTACGCGGCCGCTCGAGCAGAAACTCATCTCAGAAGAGGATCTGGCAGCAAATGATATCCTGGATT ACAAGGATGACGACGATAAGGTTTAA
Restriction Sites	SgfI-MluI
ACCN	NM_001286437
Insert Size	1935 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).
OTI Annotation	Clone contains native stop codon, and expresses the complete ORF without any c-terminal tag.
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_001286437.1, NP_001273366.1
RefSeq Size	3560 bp
RefSeq ORF	1935 bp
Locus ID	212986
UniProt ID	Q8BTY8
Gene Summary	May be involved in protein transport.[UniProtKB/Swiss-Prot Function] Transcript Variant: This variant (c) lacks an alternate in-frame exon in the 3' coding region, compared to variant a. It encodes isoform c, which is shorter than isoform a. 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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