Difference between revisions of "Submitting 10 casein and FAM20C in pD1214 plasmids for sequencing 30Sep2014"
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*'''Sequencing Strategy & Methods:''' | *'''Sequencing Strategy & Methods:''' | ||
**Submitting 10uL aliquots of 16 samples, detailed in table | **Submitting 10uL aliquots of 16 samples, detailed in table below, including 10 new casein and FAM20C in pD1214 constructs. | ||
***4 samples submitted in plasmid preps performed on two separate ''E. coli'' clones: | ***4 samples submitted in duplicate -- plasmid preps performed on two separate ''E. coli'' clones: | ||
**** P.FAKS.humBetaS:pD1214, as previously problematic construct with few transformed colonies (See [[Troubleshooting failed 12Sep2014 transformation of P.FAKS.humBeta.S]] for details.) | **** P.FAKS.humBetaS:pD1214, as previously problematic construct with few transformed colonies (See [[Troubleshooting failed 12Sep2014 transformation of P.FAKS.humBeta.S]] for details.) | ||
**** P.FAKSbovBetaB:pD121, FAM20C Kex(+):pD1214 and FAM20C Kex(-):pD1214, as plasmid inserts may not be what we expect. (See [[Cloning bovine beta casein, Fam20C (Kex + & -), from 27Sep2014]], "Results and Discussion" September 28, 2014.) | **** P.FAKSbovBetaB:pD121, FAM20C Kex(+):pD1214 and FAM20C Kex(-):pD1214, as plasmid inserts may not be what we expect. (See [[Cloning bovine beta casein, Fam20C (Kex + & -), from 27Sep2014]], "Results and Discussion" September 28, 2014.) | ||
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'''Details for 31 sequencing reactions on 16 samples:''' | '''Details for 31 sequencing reactions on 16 samples:''' | ||
[[File:Samples details from Sequetech sequence pick-up, 30Sep2014.png]] | [[File:Samples details from Sequetech sequence pick-up, 30Sep2014.png|600px]] | ||
'''Sequencing Analysis Summary Table (October 1, 2014)''' | |||
[[File:Screen_Shot_2014-10-01_at_4.42.46_PM.png|600px]] | |||
''' ''Clone 9A is also poor. Need to remove from stocks.'' ''' | |||
*'''Discussion:''' Of the 11 sequencing reactions we were able to evaluate (excluding all FAM20C, as insufficient length, and Electra cloning negative, as didn't align), there were confirmed issues with 3/11 (27.3%): incorrect sequences for bovine alpha S2 Kex+ (#3) & human beta (#4.2) and what looks like poor template DNA for human kappa Kex- (#5). Given that rate, suggest prepping and submitting two separate clones for each construct in the future. | |||
Latest revision as of 07:57, 16 October 2014
September 30, 2014: DNA pick-up by Sequetech to sequence 16 samples, detailed below
- Location: BioCurious
- Participants: Rachel (set up sample pick-up), Emi (gave samples to Sequetech rep)
- Aims: Confirm correct DNA sequence of our casein and FAM20C inserts in pD1214 vector. Trouble shoot Electra cloning negative control positive colonies (See Cloning bovine beta casein, Fam20C (Kex + & -), from 27Sep2014, "Results and Discussion" September 28, 2014.) Confirm identity of unclearly labeled DNA, prob. hKcasein Kex+ in pD1214.
- Sequencing Strategy & Methods:
- Submitting 10uL aliquots of 16 samples, detailed in table below, including 10 new casein and FAM20C in pD1214 constructs.
- 4 samples submitted in duplicate -- plasmid preps performed on two separate E. coli clones:
- P.FAKS.humBetaS:pD1214, as previously problematic construct with few transformed colonies (See Troubleshooting failed 12Sep2014 transformation of P.FAKS.humBeta.S for details.)
- P.FAKSbovBetaB:pD121, FAM20C Kex(+):pD1214 and FAM20C Kex(-):pD1214, as plasmid inserts may not be what we expect. (See Cloning bovine beta casein, Fam20C (Kex + & -), from 27Sep2014, "Results and Discussion" September 28, 2014.)
- NOTE: DNA concentration for bovAlphaS2 Kex(+) very low. May have to repeat plasmid prep.
- 4 samples submitted in duplicate -- plasmid preps performed on two separate E. coli clones:
- Sequetech rep. collected samples at ~2:00pm today.
- All except hkk+R to be sequenced in two reactions: the forward (with primer TEF-264-FW) and reverse (with primer PMYR3) directions. Sample hkk+R sampled in single direction as was likely the sample already sequenced in both directions, September 5, 2014.
- TEF-264-FW is a custom primer synthesized through Sequetech: primer sequence recommended by DNA 2.0, suppliers of pD1214. This primer will be maintained in-house for future sequencing reactions. (Note change from sequencing described August 6, 2014, as previous forward primer, Alpha-factor 146-forward, anneals to the FAKS sequence, now inside our redesigned DNA inserts.) See for primer map.
- PMYR3 is an in-house Sequetech primer.
- Submitting 10uL aliquots of 16 samples, detailed in table below, including 10 new casein and FAM20C in pD1214 constructs.
Primer Sequences TEF-264-FW: 5’ TCGATGACCTCCCATTGA 3’ Binds to TEF promoter and reads through in the 5'-3' direction (N-terminus of signal peptide). PMYR3: 5' CTTCCTTTTCGGTTAGAG 3' Binds to the terminator (CYC1) and reads through in the 3'-5' direction (C-terminus of casein).
Location of sequencing primers indicated by small purple arrows on map of pD1214:
Details for 31 sequencing reactions on 16 samples:
Sequencing Analysis Summary Table (October 1, 2014)
Clone 9A is also poor. Need to remove from stocks.
- Discussion: Of the 11 sequencing reactions we were able to evaluate (excluding all FAM20C, as insufficient length, and Electra cloning negative, as didn't align), there were confirmed issues with 3/11 (27.3%): incorrect sequences for bovine alpha S2 Kex+ (#3) & human beta (#4.2) and what looks like poor template DNA for human kappa Kex- (#5). Given that rate, suggest prepping and submitting two separate clones for each construct in the future.