Addgene pFPL-Cg Sequencing Result - Sequence Analyzer Skip to main content
Addgene

Sequence Analyzer: pFPL-Cg Sequencing Result


Map View

800 600 400 200 End (807) BpmI (698) NmeAIII (609) EXFP-R (560 .. 579) PfoI * (534) BtsI BtsαI (467) BssSI - BssSαI (434) BsrFI (404) BtgZI (375) EaeI (325) EGFP-N (299 .. 320) BanI (289) BseRI (284) BamHI (246) SmaI (244) ApaI - BanII (243) AvaI - XmaI - BsoBI - TspMI (242) PspOMI - EcoO109I (239) BsrGI (222) HincII (106) AccI (105) SalI (104) PstI (102) SfcI (98) BfuAI - BspMI (91) Start (0) attR2 VN173 pFPL-Cg 807 bp

Sequence View

Start (0) 60 g t g g c t g a t c t c a g c c a c c g c g a a a a t g a c a t c a a a a a c g c c a t t a a c c t g a t g t t c t g g c a c c g a c t a g a g t c g g t g g c g c t t t t a c t g t a g t t t t t g c g g t a a t t g g a c t a c a a g a c c

BspMIBfuAISfcIPstISalIAccIHincII 120 attR2 g g a a t a t a a a t g t c a g g c t c c c t t a t a c a c a g c c a g t c t g c a g g t c g a c c a t a g t g a c t g c c t t a t a t t t a c a g t c c g a g g g a a t a t g t g t c g g t c a g a c g t c c a g c t g g t a t c a c t g a c

180 attR2 g a t a t g t t g t g t t t t a c a g t a t t a t g t a g t c t g t t t t t t a t g c a a a a t c t a a t t t a a t a t c t a t a c a a c a c a a a a t g t c a t a a t a c a t c a g a c a a a a a a t a c g t t t t a g a t t a a a t t a t a

EcoO109IPspOMIBsrGI 240 attR2 *SEQVFHHYP a t t g a t a t t t a t a t c a t t t t a c g t t t c t c g t t c a g c t t t c t t g t a c a a a g t g g t g a t a g g t a a c t a t a a a t a t a g t a a a a t g c a a a g a g c a a g t c g a a a g a a c a t g t t t c a c c a c t a t c c

BanIBseRITspMIBsoBIXmaIAvaIBanIIApaISmaIBamHI 300 1 M 1a V 5 10 15 SKGEELFTGVVPIL VN173 G A EGFP-N MVSKGEELFTGVVPIL GPDQHHALALLQEGPHHGDQ g c c c g g g a t c c t g a t g g t g a g c a a g g g c g a g g a g c t g t t c a c c g g g g t g g t g c c c a t c c t c g g g c c c t a g g a c t a c c a c t c g t t c c c g c t c c t c g a c a a g t g g c c c c a c c a c g g g t a g g a

EaeI 360 20 25 30 35 VELDGDVNGHKFSVSGEGEG VN173 C C A G C T C G A C C T G C C G C T G C EGFP-N VELDGDVNGHKFSVSGEGEG DLQVAVYVAVLEAHGALALA g g t c g a g c t g g a c g g c g a c g t a a a c g g c c a c a a g t t c a g c g t g t c c g g c g a g g g c g a g g g c c a g c t c g a c c t g c c g c t g c a t t t g c c g g t g t t c a a g t c g c a c a g g c c g c t c c c g c t c c c

BsrFIBtgZI 420 40 45 50 55 DATYGKLTLKFICTTGKLPV VN173 DATYGKLTLKFICTTGKLPV IGGVALQGQLEDAGGALQGH c g a t g c c a c c t a c g g c a a g c t g a c c c t g a a g t t c a t c t g c a c c a c c g g c a a g c t g c c c g t g c t a c g g t g g a t g c c g t t c g a c t g g g a c t t c a a g t a g a c g t g g t g g c c g t t c g a c g g g c a

BtsαIBtsIBssSαIBssSI 480 60 65 70 75 PWPTLVTTLTWGVQCFSRYP VN173 PWPTLVTTLTWGVQCFSRYP GPGGEHGGQGPAHLAEAAVG g c c c t g g c c c a c c c t c g t g a c c a c c c t g a c c t g g g g c g t g c a g t g c t t c a g c c g c t a c c c c g g g a c c g g g t g g g a g c a c t g g t g g g a c t g g a c c c c g c a c g t c a c g a a g t c g g c g a t g g g

PfoI* 540 80 85 90 95 DHMKQHDFFKSAMPEGYVQE VN173 DHMKQHDFFKSAMPEGYVQE VVHLLVVEELGGHGFAVDLL c g a c c a c a t g a a g c a g c a c g a c t t c t t c a a g t c c g c c a t g c c c g a a g g c t a c g t c c a g g a g c t g g t g t a c t t c g t c g t g c t g a a g a a g t t c a g g c g g t a c g g g c t t c c g a t g c a g g t c c t

600 100 105 110 115 RTIFFKDDGNYKTRAEVKFE VN173 C T G C T G C C G T T G A T G T T C T G EXFP-R RTIFFKDDGNYKTRAEVKFE AGDEELVVAVVLGAGLHLEL g c g c a c c a t c t t c t t c a a g g a c g a c g g c a a c t a c a a g a c c c g c g c c g a g g t g a a g t t c g a c g c g t g g t a g a a g a a g t t c c t g c t g c c g t t g a t g t t c t g g g c g c g g c t c c a c t t c a a g c t

NmeAIII 660 120 125 130 135 GDTLVNRIELKGIDFKEDGN VN173 GDTLVNRIELKGIDFKEDGN AVGQHVADLQLADVELLVAV g g g c g a c a c c c t g g t g a a c c g c a t c g a g c t g a a g g g c a t c g a c t t c a a g g a g g a c g g c a a c c c g c t g t g g g a c c a c t t g g c g t a g c t c g a c t t c c c g t a g c t g a a g t t c c t c c t g c c g t t

BpmI 720 140 145 150 155 ILGHKLEYNYISHNVYITAD VN173 ILGHKLEYNYISHNVYITAD DQPVLQLVVVDAVVDIDGGV c a t c c t g g g g c a c a a g c t g g a g t a c a a c t a c a t c a g c c a c a a c g t c t a t a t c a c c g c c g a g t a g g a c c c c g t g t t c g a c c t c a t g t t g a t g t a g t c g g t g t t g c a g a t a t a g t g g c g g c t

780 160 165 170 KQKNGIKANFKIRHNIE DGS VN173 KQKNGIKANFKIRHNIEDGS LLLVADLGVELDAVVDLVAA c a a g c a g a a g a a c g g c a t c a a g g c c a a c t t c a a g a t c c g c c a c a a c a t c g a g g a c g g c a g g t t c g t c t t c t t g c c g t a g t t c c g g t t g a a g t t c t a g g c g g t g t t g t a g c t c c t g c c g t c

End (807) 807 (in frame with VN173) VQLADHYQ VQLADHYQ HLEGVVVL c g t g c a g c t c g c c g a c c a c t a c c a g c a g c a c g t c g a g c g g c t g g t g a t g g t c g 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.