Addgene pUC118-mCtnnb1-FLIP-Puro Sequencing Result - Sequence Analyzer Skip to main content
Addgene

Sequence Analyzer: pUC118-mCtnnb1-FLIP-Puro Sequencing Result


Map View

800 600 400 200 End (921) CsiI - SexAI * (877) Bpu10I (847) PmlI - BsaAI (837) AflIII (834) PflMI - HaeII (758) AfeI (756) SphI (707) Esp3I - BsmBI (681) BsrDI (652) EciI (588) XcmI (553) BlpI (541) BmtI (509) NheI (505) BmrI (449) HincII (413) Bsu36I (397) XmnI (347) AlwNI (313) BtgI - StyI - NcoI (280) MscI (279) XbaI (240) BamHI (234) SmaI (231) AvaI - KpnI - XmaI - BsoBI - TspMI (229) Acc65I (225) SacI - BsiHKAI (223) Eco53kI (221) ApoI - EcoRI (213) M13 rev M13 Reverse (187 .. 203) BsrBI (169) M13/pUC Reverse (168 .. 190) Start (0) CAP binding site lac promoter lac operator BC2 tag pUC118-mCtnnb1-FLIP-Puro 921 bp

Sequence View

Start (0) 5ʹ 3ʹ 60 c g c c t c t c c c c g c g c g t t g g c c g a t t c a t t a a t g c a g c t g g c a c g a c a g g t t t c c c g a c t g c g g a g a g g g g c g c g c a a c c g g c t a a g t a a t t a c g t c g a c c g t g c t g t c c a a a g g g c t g a

120 CAP binding site g g a a a g c g g g c a g t g a g c g c a a c g c a a t t a a t g t g a g t t a g c t c a c t c a t t a g g c a c c c c c c t t t c g c c c g t c a c t c g c g t t g c g t t a a t t a c a c t c a a t c g a g t g a g t a a t c c g t g g g g

BsrBI 180 -35 -10 lac promoter lac operator A G C G G A T A A C A A T M13/pUC Reverse *VKHKRSTHQTSNHASLL a g g c t t t a c a c t t t a t g c t t c c g g c t c g t a t g t t g t g t g g a a t t g t g a g c g g a t a a c a a t t c c g a a a t g t g a a a t a c g a a g g c c g a g c a t a c a a c a c a c c t t a a c a c t c g c c t a t t g t t a

EcoRIApoIEco53kIBsiHKAISacIAcc65ITspMIBsoBIXmaIKpnIAvaISmaIBamHI 240 M13 rev T T C A C A C A G G M13/pUC Reverse C A G G A A A C A G C T A T G A C M13 Reverse KVCSVAIVMIVFELETGPSG t t c a c a c a g g a a a c a g c t a t g a c c a t g a t t a c g a a t t c g a g c t c g g t a c c c g g g g a t c c t a a g t g t g t c c t t t g t c g a t a c t g g t a c t a a t g c t t a a g c t c g a g c c a t g g g c c c c t a g g a

MscINcoIStyIBtgIXbaI 300 1 PDRK BC2 tag RSDHCSVQHLQVHGHLRVSF c t a g a g t c g t g a c a g c t g a c c t g a t g g a g t t g g a c a t g g c c a t g g a g c c g g a c a g a a a a g g a t c t c a g c a c t g t c g a c t g g a c t a c c t c a a c c t g t a c c g g t a c c t c g g c c t g t c t t t t c

XmnIAlwNI 360 5 10 AAVSHWQQ (in frame with BC2 tag) QSYLDSGIHSGA BC2 tag SSDAVPLLLRVQIRSDMRTG c t g c t g t c a g c c a c t g g c a g c a g c a g t c t t a c t t g g a t t c t g g a a t c c a t t c t g g t g c c a g a c g a c a g t c g g t g a c c g t c g t c g t c a g a a t g a a c c t a a g a c c t t a g g t a a g a c c a c g g t

HincIIBsu36I 420 (in frame with BC2 tag) TTTAPSLSGKGNPEEEDVDT GGCSRGQTALAVRLFFINVG c c a c c a c a g c t c c t t c c c t g a g t g g c a a g g g c a a c c c t g a g g a a g a a g a t g t t g a c a c c t g g t g g t g t c g a g g a a g g g a c t c a c c g t t c c c g t t g g g a c t c c t t c t t c t a c a a c t g t g g a

BmrI 480 (in frame with BC2 tag) SQVLYEWEQGFSQSFTQEQV GLDKIFPLLAKGLGERLLLY c c c a a g t c c t t t a t g a a t g g g a g c a a g g c t t t t c c c a g t c c t t c a c g c a a g a g c a a g t a g g g g t t c a g g a a a t a c t t a c c c t c g t t c c g a a a a g g g t c a g g a a g t g c g t t c t c g t t c a t c

BmtINheI 540 (in frame with BC2 tag) AGKAFVFGS* STFCKHKSALMLNRSLATHC c t g g t a a a g c a t t t g t g t t t g g a a g c t a g c a t t a a g t t t c t t g a c a g g g c t g t g t g a c a g g a c c a t t t c g t a a a c a c a a a c c t t c g a t c g t a a t t c a a a g a a c t g t c c c g a c a c a c t g t c

EciIXcmIBlpI 600 SLWLVLPNFSPRLTASDWM c t c a g c c a c a g c a c a a g t g g g t t g a a g g a a g g g c g g a g g g t a g c g g a g t c c c a c a t g c c t g a g t c g g t g t c g t g t t c a c c c a a c t t c c t t c c c g c c t c c c a t c g c c t c a g g g t g t a c g g a

BsrDI 660 a g t g a g t g t t g g a t t t a c c t t t t t c a g a t a t t g a c g g g c a g t a t g c a a t g a c t a g g g c t c t c a c t c a c a a c c t a a a t g g a a a a a g t c t a t a a c t g c c c g t c a t a c g t t a c t g a t c c c g a g

SphIBsmBIEsp3I 720 a g a g g g t c c g a g c t g c c a t g t t c c c t g a g a c g c t a g a t g a g g g c a t g c a g a t c c c a t c c a t c t c c c a g g c t c g a c g g t a c a a g g g a c t c t g c g a t c t a c t c c c g t a c g t c t a g g g t a g g t

AfeIHaeIIPflMI 780 c g c a g t t t g a c g c t g c t c a t c c c a c t a a t g t c c a g c g c t t g g c t g a a c c a t c a c a g a t g t g c g t c a a a c t g c g a c g a g t a g g g t g a t t a c a g g t c g c g a a c c g a c t t g g t a g t g t c t a c a

AflIIIBsaAIPmlI 840 t g a a a c a t g c a g t t g t c a a t t t g a t t a a c t a t c a g g a t g a c g c g g a a c t t g c c a c a c g t g a c t t t g t a c g t c a a c a g t t a a a c t a a t t g a t a g t c c t a c t g c g c c t t g a a c g g t g t g c a c

SexAI*CsiIBpu10I 900 c a a t t c c t g a g c t g a c a a a a c t g c t a a a c g a t g a g g a c c a g g t a a g c a g t g a t g t a a c t t g t t a a g g a c t c g a c t g t t t t g a c g a t t t g c t a c t c c t g g t c c a t t c g t c a c t a c a t t g a a

End (921) 3ʹ 5ʹ 921 g c t t t t c a g t t t a c t t t g a g g c g a a a a g t c a a a t g a a a c t c c

Restriction Enzymes

Instructions: By default, all cutters are shown. Filter on number of cut sites or search by enzyme name.

Filter

Features

Primers

BLAST

BLAST (Basic Local Alignment Search Tool) finds regions of similarity between biological sequences. Click on the buttons below to submit a BLAST search to NCBI. The results will appear in a new window. See your recent BLAST results on NCBI's website.

  • Nucleotide-Nucleotide BLAST (BLASTN)

  • Translated Nucleotide-Protein BLAST (BLASTX)

  • Sequence alignment using BLAST (BLAST2)

Sequence Analyzer Guide

Map

Displays a graphical map based on nucleotide sequence data labeled with restriction enzymes, plasmid features, ORFs (theoretical open reading frames) and primers. Hovering over data labels will display additional information (e.g. cut site)

To select a portion of sequence, click one location on the plasmid and then a second location to display the sequence between the two locations.

Sequence

Displays both strands of base paired nucleotide sequences with annotated enzymes, plasmid features, ORFs (theoretical open reading frames) and primers. Hovering over data labels will display additional information (e.g. cut site).

To select a portion of sequence, click one location on the sequence and then a second location to display the sequence between the two locations.

Enzymes

List of restriction enzymes that can cut a given nucleotide sequence. Table lists enzyme name and the sequence location of the cut.

Features

List of common features detected in a given nucleotide sequence. Table lists feature name, location, size, color used to indicate its position on the map, and direction (if relevant).

Primers

List of commonly used primers detected in a given nucleotide sequence. Table lists primer name, sequence, length, binding site location, and direction.

BLAST

Use Basic Local Alignment Search Tool (BLAST) via the NCBI website to determine similarity between a given sequence and nucleotide (BLASTN) or protein (BLASTX) sequence databases. Additionally, align a custom nucleotide sequence against a given sequence using BLAST2.

File Downloads

GenBank

File contains the nucleotide sequence and annotated features in GenBank flat file format. Open the file with a text editor or plasmid mapping software to view the sequence.

SnapGene

File contains the nucleotide sequence and enhanced annotations from SnapGene Server. Open the file with SnapGene software or the free Viewer to view the plasmid map, sequence, and perform additional sequence analysis.