Addgene pCS2+8CmCherry-ABCC1 Sequencing Result - Sequence Analyzer Skip to main content
Addgene

Sequence Analyzer: pCS2+8CmCherry-ABCC1 Sequencing Result


Map View

600 400 200 End (777) PvuI - BsiEI - AsiSI (767) ClaI - BspDI (753) MscI (718) BsiHKAI (688) ApaLI (684) BanII (677) BssSI - BssSαI (657) mCherry-R (586 .. 604) AhdI (555) BsaAI (518) PstI - SbfI (397) mCherry-F (317 .. 336) PflMI (312) BtgI - NcoI (311) BbsI - PspFI (309) BseYI (305) BsrBI (290) AlwNI (245) DrdI (210) BbvCI - Bpu10I (207) PvuII - MspA1I (170) BsgI (156) HincII (149) AleI - MslI (106) BsrFI - XcmI - SgrAI (63) NmeAIII (62) TatI - BsrGI (44) ApoI - EcoRI (33) SmlI - XhoI - PaeR7I (20) XbaI (12) Start (0) mCherry pCS2+8CmCherry-ABCC1 777 bp

Sequence View

BsrGITatIEcoRIApoIPaeR7IXhoISmlIXbaIStart (0) 5ʹ 3ʹ 60 235 *KYLEDM mCherry HYSSRGSRGLEFLLVQLVH *KYLEDM c t c a c t a t a g t t c t a g a g g c t c g a g a g g c c t t g a a t t c t t a c t t g t a c a g c t c g t c c a t g g a g t g a t a t c a a g a t c t c c g a g c t c t c c g g a a c t t a a g a a t g a a c a t g t c g a g c a g g t a c

MslIAleINmeAIIISgrAIXcmIBsrFI 120 230 225 220 215 GGTSHRGEAREYQEVITYDE mCherry AAGGVAALGAFVLFHDGVVL GGTSHRGEAREYQEVITYDE c c g c c g g t g g a g t g g c g g c c c t c g g c g c g t t c g t a c t g t t c c a c g a t g g t g t a g t c c t c g g g c g g c c a c c t c a c c g c c g g g a g c c g c g c a a g c a t g a c a a g g t g c t a c c a c a t c a g g a g c

MspA1IPvuIIBsgIHincII 180 210 205 200 195 NHSTIDLKINVNYAGPLQVP mCherry VVGGDVQLDVDVVGAGQLHG NHSTIDLKINVNYAGPLQVP t t g t g g g a g g t g a t g t c c a a c t t g a t g t t g a c g t t g t a g g c g c c g g g c a g c t g c a c g g g c a a c a c c c t c c a c t a c a g g t t g a a c t a c a a c t g c a a c a t c c g c g g c c c g t c g a c g t g c c c g

Bpu10IBbvCIDrdI 240 190 185 180 175 KKAKYTTKVEADYHGGDKLK mCherry LLGLVGGLDLSVVVAAVLQL KKAKYTTKVEADYHGGDKLK t t c t t g g c c t t g t a g g t g g t c t t g a c c t c a g c g t c g t a g t g g c c g c c g t c c t t c a g c t t c a a g a a c c g g a a c a t c c a c c a g a a c t g g a g t c g c a g c a t c a c c g g c g g c a g g a a g t c g a a g

BsrBIAlwNI 300 170 165 160 155 LRQKIEGKLAGDEPYMRESS mCherry QPLLDLALQGAVLGVHPLGG LRQKIEGKLAGDEPYMRESS a g c c t c t g c t t g a t c t c g c c c t t c a g g g c g c c g t c c t c g g g g t a c a t c c g c t c g g a g g a g t c g g a g a c g a a c t a g a g c g g g a a g t c c c g c g g c a g g a g c c c c a t g t a g g c g a g c c t c c t c

BseYIPspFIBbsINcoIBtgIPflMI 360 150 145 140 135 AEWGMTKKQMVPGDSPFNTG mCherry A G A A G A A G A C G T A A T G C C C C mCherry-F GLPAHGLLLHYGAVGGEVGA AEWGMTKKQMVPGDSPFNTG g c c t c c c a g c c c a t g g t c t t c t t c t g c a t t a c g g g g c c g t c g g a g g g g a a g t t g g t g c c g c g g a g g g t c g g g t a c c a g a a g a a g a c g t a a t g c c c c g g c a g c c t c c c c t t c a a c c a c g g c

SbfIPstI 420 130 125 120 115 RLKVKYIFEGDQLSSDQTVT mCherry AQLHLVDELAVLQGGVLGHG RLKVKYIFEGDQLSSDQTVT c g c a g c t t c a c c t t g t a g a t g a a c t c g c c g t c c t g c a g g g a g g a g t c c t g g g t c a c g g t c g c g t c g a a g t g g a a c a t c t a c t t g a g c g g c a g g a c g t c c c t c c t c a g g a c c c a g t g c c a g

480 110 105 100 95 VVGGDEFNMVREWKFGEPFS mCherry HHAAVLEVHHALPLEALGEG VVGGDEFNMVREWKFGEPFS a c c a c g c c g c c g t c c t c g a a g t t c a t c a c g c g c t c c c a c t t g a a g c c c t c g g g g a a g g a c t g g t g c g g c g g c a g g a g c t t c a a g t a g t g c g c g a g g g t g a a c t t c g g g a g c c c c t t c c t g

BsaAI 540 90 85 80 75 LKLYDPIDAPHKVYAKSGYM mCherry QLQVVGDVGGVLHVGLGAVH LKLYDPIDAPHKVYAKSGYM a g c t t c a a g t a g t c g g g g a t g t c g g c g g g g t g c t t c a c g t a g g c c t t g g a g c c g t a c a t g t c g a a g t t c a t c a g c c c c t a c a g c c g c c c c a c g a a g t g c a t c c g g a a c c t c g g c a t g t a c

AhdI 600 70 65 60 55 FQPSLIDWAFPLPGGKTVKL mCherry T T G G T C A C C T T C A G C mCherry-R ELRGQDVPGEGQGATLGHLQ FQPSLIDWAFPLPGGKTVKL a a c t g a g g g g a c a g g a t g t c c c a g g c g a a g g g c a g g g g g c c a c c c t t g g t c a c c t t c a g c t t g a c t c c c c t g t c c t a c a g g g t c c g c t t c c c g t c c c c c g g t g g g a a c c a g t g g a a g t c g

BssSαIBssSI 660 50 45 40 35 KATQTGEYPRGEGEGEIEFE mCherry T T G G mCherry-R LGGLGALVGAALALALDLEL KATQTGEYPRGEGEGEIEFE t t g g c g g t c t g g g t g c c c t c g t a g g g g c g g c c c t c g c c c t c g c c c t c g a t c t c g a a c t c g a a c c g c c a g a c c c a c g g g a g c a t c c c c g c c g g g a g c g g g a g c g g g a g c t a g a g c t t g a g c

MscIBanIIApaLIBsiHKAI 720 30 25 20 15 HGNVSGEMHVKFRMFEKIIA mCherry VAVHGALHVHLEAHELLDDG HGNVSGEMHVKFRMFEKIIA t g g c c g t t c a c g g a g c c c t c c a t g t g c a c c t t g a a g c g c a t g a a c t c c t t g a t g a t g g c c a c c g g c a a g t g c c t c g g g a g g t a c a c g t g g a a c t t c g c g t a c t t g a g g a a c t a c t a c c g g

End (777) AsiSIBsiEIPvuIBspDIClaI 3ʹ 5ʹ 777 10 5 1 MNDEEGKSVM mCherry HVILLALAHHQSMSGDRWP MNDEEGKSVMLRHGAIAPR a t g t t a t c c t c c t c g c c c t t g c t c a c c a t c a a t c g a t g t c c g g c g a t c g c t g g c c g g t a c a a t a g g a g g a g c g g g a a c g a g t g g t a g t t a g c t a c a g g c c g c t a g c g a c c g g 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.