Addgene RKS-Fzd7/8 subtype NGS Wnt - Sequence Analyzer Skip to main content
Addgene

Sequence Analyzer: RKS-Fzd7/8 subtype NGS Wnt


Map View

800 600 400 200 End (966) BsiEI (935) NotI - EagI (932) BfuAI - PaqCI - BspMI (925) MmeI (920) BsgI (895) StuI (892) BsaBI * (884) BglII (827) BsiHKAI (793) ApaLI (789) BsrFI (765) PpuMI - EcoO109I (704) Bsu36I (700) BstAPI (695) XmnI (636) PspXI (625) BsrDI (597) AseI (514) AatII (338) ZraI (336) BsaHI (335) BsmI (246) HpaI - HincII (141) BclI * (74) BmrI (70) BamHI (49) Bpu10I (19) BbsI (10) Start (0) 8xHis RKS-Fzd7/8 subtype NGS Wnt 966 bp

Sequence View

BamHIBpu10IBbsIStart (0) 60 MKTIIALSYIFCLVFAGSSE a t g a a g a c c a t c a t c g c c c t g a g c t a c a t c t t c t g c c t g g t g t t c g c c g g a t c c t c t g a a t a c t t c t g g t a g t a g c g g g a c t c g a t g t a g a a g a c g g a c c a c a a g c g g c c t a g g a g a c t t

BmrIBclI* 120 LGTRLIRAALDGNKDRVKDL c t g g g t a c g c g t c t g a t c a g g g c a g c a t t a g a c g g t a a c a a a g a c c g t g t t a a a g a c c t c g a c c c a t g c g c a g a c t a g t c c c g t c g t a a t c t g c c a t t g t t t c t g g c a c a a t t t c t g g a g

HincIIHpaI 180 IENGADVNASLMSGATPLHA a t t g a a a a t g g t g c t g a c g t t a a c g c g t c c c t t a t g t c t g g g g c g a c t c c g t t a c a c g c c t a a c t t t t a c c a c g a c t g c a a t t g c g c a g g g a a t a c a g a c c c c g c t g a g g c a a t g t g c g g

240 AAMNGHKEVVKLLISKGADV g c c g c c a t g a a c g g c c a c a a a g a g g t t g t g a a g t t a c t g a t c t c c a a g g g c g c a g a t g t g c g g c g g t a c t t g c c g g t g t t t c t c c a a c a c t t c a a t g a c t a g a g g t t c c c g c g t c t a c a c

BsmI 300 NAQSVAGSTPLDAAAFSGHK a a t g c t c a g t c c g t t g c g g g t t c t a c a c c t c t g g a t g c g g c g g c g t t t a g t g g a c a t a a a t t a c g a g t c a g g c a a c g c c c a a g a t g t g g a g a c c t a c g c c g c c g c a a a t c a c c t g t a t t t

BsaHIZraIAatII 360 EVVKLLISKGADVNAVNAAG g a a g t g g t a a a a c t g c t g a t a a g t a a a g g a g c a g a c g t c a a t g c t g t t a a t g c g g c t g g a c t t c a c c a t t t t g a c g a c t a t t c a t t t c c t c g t c t g c a g t t a c g a c a a t t a c g c c g a c c t

420 LTPLHAAADNGHKEVVKLLI t t g a c c c c c c t a c a t g c t g c t g c t g a t a a t g g g c a c a a g g a a g t a g t g a a g t t g c t t a t t a a c t g g g g g g a t g t a c g a c g a c g a c t a t t a c c c g t g t t c c t t c a t c a c t t c a a c g a a t a a

480 SKGADVNAKADHGMTPLHFA t c t a a g g g g g c c g a c g t a a a t g c g a a a g c t g a c c a t g g c a t g a c t c c a c t c c a t t t c g c a a g a t t c c c c c g g c t g c a t t t a c g c t t t c g a c t g g t a c c g t a c t g a g g t g a g g t a a a g c g t

AseI 540 AQRGHKEVVKLLISKGADLN *DAFTRIQV g c a c a g c g c g g t c a t a a g g a a g t c g t t a a a c t a t t a a t c a g c a a a g g t g c g g a t t t g a a c c g t g t c g c g c c a g t a t t c c t t c a g c a a t t t g a t a a t t a g t c g t t t c c a c g c c t a a a c t t g

BsrDI 600 TSAKDGATPLDMARESGNEE GRGFVTCGRKVHRTFRAILL a c c t c t g c c a a a g a c g g t g c a a c c c c g c t t g a c a t g g c g c g t g a a t c t g g c a a t g a g g a g t g g a g a c g g t t t c t g c c a c g t t g g g g c g a a c t g t a c c g c g c a c t t a g a c c g t t a c t c c t c

XmnIPspXI 660 VVKLLEKQLEGSGSGGSGSG NDLEQFLLELSATGSTRAGS g t t g t c a a g c t c t t g g a a a a g c a a c t c g a g g g a a g c g g t t c c g g a g g t t c t g g c t c c g g a c a a c a g t t c g a g a a c c t t t t c g t t g a g c t c c c t t c g c c a a g g c c t c c a a g a c c g a g g c c t

BstAPIBsu36IEcoO109IPpuMI 720 KMYHTKGQEGSVCLRSSDCA FHIVSLSLFAAHAQPGRVTC a a a a t g t a t c a c a c t a a g g g a c a g g a a g g c a g c g t g t g c c t g a g g t c c t c t g a c t g t g c a t t t t a c a t a g t g t g a t t c c c t g t c c t t c c g t c g c a c a c g g a c t c c a g g a g a c t g a c a c g t

BsrFI 780 SGLCCARHFWSKICKPVLKE RAQAAGSVKPGFDALRNQFL t c t g g c c t g t g c t g c g c c a g a c a c t t t t g g t c c a a a a t c t g c a a g c c g g t t c t g a a a g a g a g a c c g g a c a c g a c g c g g t c t g t g a a a a c c a g g t t t t a g a c g t t c g g c c a a g a c t t t c t c

BglIIApaLIBsiHKAI 840 GQVCTKHRRKGSHGLEIFQR ALHACLMSSLAAMSELDKLP g g c c a g g t g t g c a c a a a g c a t c g a c g a a a g g g c a g c c a t g g a c t c g a g a t c t t t c a g a g g c c g g t c c a c a c g t g t t t c g t a g c t g c t t t c c c g t c g g t a c c t g a g c t c t a g a a a g t c t c c

StuIBsgIBsaBI* 900 CYCGEGLSCRIQKDHHQASN AVAPLTQRASDLFIMMLGGV t g c t a c t g c g g g g a g g g t c t g t c t t g c a g a a t c c a g a a a g a t c a t c a t c a g g c c t c c a a c a c g a t g a c g c c c c t c c c a g a c a g a a c g t c t t a g g t c t t t c t a g t a g t a g t c c g g a g g t t g

MmeIBspMIPaqCIBfuAIEagINotIBsiEI 960 1 5 HHHHHHH 8xHis SSRLHTCQRHAAAHHHHHHH GGAQVGALSMRGRMMVVMVV t c c t c c c g c c t g c a c a c c t g c c a g c g a c a t g c g g c c g c g c a t c a t c a c c a c c a t c a c c a c a g g a g g g c g g a c g t g t g g a c g g t c g c t g t a c g c c g g c g c g t a g t a g t g g t g g t a g t g g t g

End (966) 966 H * 8xHis H* ML c a t t a a g t a a t t

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.