Tag Archives: Haliotis rufescens

DNA Quantification – Ava’s RLO Trasmission Samples

Quantified DNA extractions from Ava’s samples that I isolated earlier this month, as well as some older samples that I hadn’t quantified yet.

Used the Roberts Lab Qubit 3.0 and the Qubit dsDNA BR Kit (broad range). Used 5uL of template for the first and third groups and 1uL of template for the second group (see Results below).

All data was added to the master extraction spreadsheet (Google Sheet): ava_abalone_master_extraction_list

Results:

20171101_ava_rlo_quantification_qubit_01 (Google Sheet)

20171101_ava_rlo_quantification_qubit_02 (Google Sheet)

20171101_ava_rlo_quantification_qubit_03 (Google Sheet)

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DNA Quantification – Ava’s RLO Trasmission Samples

Quantified DNA extractions from Ava’s samples that I isolated earlier this month, as well as some older samples that I hadn’t quantified yet.

Used the Roberts Lab Qubit 3.0 and the Qubit hsDNA Kit (high sensitivity). Used 5uL of template for all samples.

All data was added to the master extraction spreadsheet (Google Sheet): ava_abalone_master_extraction_list

Results:

20171026_Ava_RLO_quantification_qubit_01 (Google Sheet)

20171026_Ava_RLO_quantification_qubit_02 (Google Sheet)

There were 65 samples with concentrations that were too high for the high sensitivity assay. Will re-quantify this samples using the broad range assay.

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qPCR – Ava’s RLO Transmission Samples

Ran five plates of qPCRs on bunch of DNA I extracted ealier this month.

Standard curve was p18RK7 from 20161128.

All samples were run in duplicate.

Master mix calcs are here (Google Sheet): 20171026_qPCR_WSN1_Ava_Samples

Plate layouts, cycling params, etc. can be seen in the corresponding qPCR Reports (see Results below).

Baseline threshold was manually set to 580, based on Lisa’s development of the withering syndrome qPCR assay.

Results:

Curves looked great on each plate. See images at bottom of post.

NOTE: Plate #5 had a missed rep; I think this was due to a bad pipette tip. I excluded the 3e4 point of the curve in the analysis.

PLATE #1

qPCR Report (PDF): Sam_2017-10-26 07-31-12_CC009827.pdf
qPCR Data File (CFX96): Sam_2017-10-26 07-31-12_CC009827.pcrd

PLATE #2

qPCR Report (PDF): Sam_2017-10-26 09-02-31_CC009827.pdf
qPCR Data File (CFX96): Sam_2017-10-26 09-02-31_CC009827.pcrd

PLATE #3

qPCR Report (PDF): Sam_2017-10-26 10-32-10_CC009827.pdf
qPCR Data File (CFX96): Sam_2017-10-26 10-32-10_CC009827.pcrd

PLATE #4

qPCR Report (PDF): Sam_2017-10-26 12-01-33_CC009827.pdf
qPCR Data File (CFX96): Sam_2017-10-26 12-01-33_CC009827.pcrd

PLATE #5

qPCR Report (PDF): Sam_2017-10-26 13-31-05_CC009827.pdf
qPCR Data File (CFX96): Sam_2017-10-26 13-31-05_CC009827.pcrd


PLATE #1


PLATE #2


PLATE #3


PLATE #4


PLATE #5

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qPCR – Ava’s RLO Transmission Samples

Ran five plates of qPCRs on bunch of DNA I extracted ealier this month.

Standard curve was p18RK7 from 20161128.

All samples were run in duplicate.

Master mix calcs are here (Google Sheet): 20171025_qPCR_WSN1_Ava_Samples

Plate layouts, cycling params, etc. can be seen in the corresponding qPCR Reports (see Results below).

Baseline threshold was manually set to 580, based on Lisa’s development of the withering syndrome qPCR assay.

Results:

Curves looked great on each plate. See images at bottom of post.

NOTE: Plate #5 had a missed rep; I think this was due to a bad pipette tip. I excluded the 3e4 point of the curve in the analysis.

PLATE #1

qPCR Report (PDF): Sam_2017-10-25 08-35-04_CC009827.pdf
qPCR Data File (CFX96): Sam_2017-10-25 08-35-04_CC009827.pcrd

PLATE #2

qPCR Report (PDF): Sam_2017-10-25 10-05-57_CC009827.pdf
qPCR Data File (CFX96): Sam_2017-10-25 10-05-57_CC009827.pcrd

PLATE #3

qPCR Report (PDF): Sam_2017-10-25 11-36-44_CC009827.pdf
qPCR Data File (CFX96): Sam_2017-10-25 11-36-44_CC009827.pcrd

PLATE #4

qPCR Report (PDF): Sam_2017-10-25 13-10-13_CC009827.pdf
qPCR Data File (CFX96): Sam_2017-10-25 13-10-13_CC009827.pcrd

PLATE #5

qPCR Report (PDF): Sam_2017-10-25 14-40-08_CC009827.pdf
qPCR Data File (CFX96): Sam_2017-10-25 14-40-08_CC009827.pcrd


PLATE #1


PLATE #2


PLATE #3


PLATE #4


PLATE #5

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DNA Isolation – Ava Withering Syndrome Transmission Study Tissues

Isolated DNA from 17 red abalone digestive gland tissue samples.

Tissue was weighed, minced with a razor blade, and transferred to 2mL snap cap tube containing 1mL of InhibtEX Buffer.

DNA was extracted using the QIAmp Fast DNA Stool Mini Kit (Qiagen) following the manufacturer’s protocol with the following options:

Minced tissue was incubated at 70C O/N.

These samples were actually incubated O/N on 20171012. I dropped the rack containing these tubes after the initial incubation and these tubes popped open and spilled.

Since I used all of the tissue, I have nothing to go back to. I’ve attempted to recover as much of the remaining supernatant in each of these tubes. I brought the volume of each tube up to 600mL with Inhibitex Buffer and proceeded with the isolations.

Followed “human DNA analysis” protocol (to maximize sample recovery)
Eluted DNA with 100μL Buffer ATE
Sample information is in this spreadsheet (Google Sheet): ava_abalone_master_extraction_list

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DNA Isolation – Ava Withering Syndrome Transmission Study Tissues

Isolated DNA from 96 red abalone digestive gland tissue samples.

Tissue was weighed, minced with a razor blade, and transferred to 2mL snap cap tube containing 1mL of InhibtEX Buffer.

DNA was extracted using the QIAmp Fast DNA Stool Mini Kit (Qiagen) following the manufacturer’s protocol with the following options:

Minced tissue was incubated at 70C O/N
Followed “human DNA analysis” protocol (to maximize sample recovery)
Eluted DNA with 100μL Buffer ATE
Sample information is in this spreadsheet (Google Sheet): ava_abalone_master_extraction_list

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DNA Isolation – Ava Withering Syndrome Transmission Study Tissues

Isolated DNA from 144 red abalone digestive gland tissue samples.

Tissue was weighed, minced with a razor blade, and transferred to 2mL snap cap tube containing 1mL of InhibtEX Buffer.

DNA was extracted using the QIAmp Fast DNA Stool Mini Kit (Qiagen) following the manufacturer’s protocol with the following options:

Minced tissue was incubated at 70C O/N
Followed “human DNA analysis” protocol (to maximize sample recovery)
Eluted DNA with 100μL Buffer ATE
Sample information is in this spreadsheet (Google Sheet): ava_abalone_master_extraction_list

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DNA Isolation – Ava Withering Syndrome Transmission Study Tissues

Isolated DNA from 58 red abalone digestive gland tissue samples.

Tissue was weighed, minced with a razor blade, and transferred to 2mL snap cap tube containing 1mL of InhibtEX Buffer.

DNA was extracted using the QIAmp Fast DNA Stool Mini Kit (Qiagen) following the manufacturer’s protocol with the following options:

  • Minced tissue was incubated at 70C O/N
  • Followed “human DNA analysis” protocol (to maximize sample recovery)
  • Eluted DNA with 100μL Buffer ATE

Sample information is in this spreadsheet (Google Sheet): ava_abalone_master_extraction_list

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DNA Isolation – Ava Withering Syndrome Transmission Study Tissues

Isolated DNA from 26 red abalone digestive gland tissue samples.

Tissue was weighed, minced with a razor blade, and transferred to 2mL snap cap tube containing 1mL of InhibtEX Buffer.

DNA was extracted using the QIAmp Fast DNA Stool Mini Kit (Qiagen) following the manufacturer’s protocol with the following options:

  • Minced tissue was incubated at 70C O/N
  • Followed “human DNA analysis” protocol (to maximize sample recovery)
  • Eluted DNA with 100μL Buffer ATE

Sample information is in this spreadsheet (Google Sheet): ava_abalone_master_extraction_list

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qPCR – Ava’s RLO Transmission Samples

Due to a wonky standard curve, I repeated the qPCR from earlier this week.

Standard curve was p18RK7 from 20161128.

All samples were run in duplicate.

Master mix calcs are here (Google Sheet): 20170619_qPCR_WSN1_Ava_Samples

Plate layouts, cycling params, etc. can be seen in the corresponding qPCR Reports (see Results below).

Baseline threshold was manually set to 580, based on Lisa’s development of the withering syndrome qPCR assay.

Results:

qPCR Report (PDF): Sam_2017-06-21 07-39-31_CC009827.pdf
qPCR Data File (CFX96): Sam_2017-06-21 07-39-31_CC009827.pcrd

 

Well, unfortunately, it looks like the curve has gone wonky. This is two consecutive runs with the same behavior. A new curve will have to be made and tested.

 

 

 

 

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