Training Quiz: Tissue-Tek Genie® ISH -Sakura Finetek USA

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1. Which of the following symbols means “MDPV”?(Required)

A) ❀

B) ✘

C) ✓

D) None

2. True or False – As a FAS in the SFA-territory, you are allowed to optimize or assist the customer in optimizing ISH-stained protocols?(Required)

A) True

B) False

3. Which of the following will display on the 2-step screen when you load/scan slides with 1 non-approved protocol variation while logged in as a lead technologist?(Required)

A) GUI will check the Abort checkbox and a “non-approved protocol assigned to slide” prompt will display when the user hovers over the “!” icon

B) GUI will check the Abort checkbox and a “Mismatch/expired slide or RDA tag label” prompt will display when the user hovers over the “!” icon

C) GUI will check the Abort checkbox for all stations, gray out the Run button, and prompt the user that the run was aborted

D) GUI will display no errors/aborts and the Run button will be available

4. To run a CISH probe, can a Genie user use a Tissue-Tek Genie® User-Fillable Cartridge for Biomarker-Binding Reagent (8622-G006) instead of a Tissue-Tek Genie® User-Fillable Cartridge for CISH Amplification Linker (9809-G006)?(Required)

A) Yes

B) No

5. A manager informs a lead technologist to change the protocol variation for an antibody from approved to non-approved. Which of the following is correct?(Required)

A) The lead technologist tells the manager they cannot change the protocol variation from approved to non-approved

B) The lead technologist opens the IHC Protocol feature, unchecks the Approved checkbox for the corresponding variation, and selects Save

C) The lead technologist opens the ISH Protocol Setup feature, unchecks the Approved checkbox for the corresponding variation, and selects Save

D) The lead technologist opens the Master Default Protocol list under System Settings, selects a new protocol variation for the respective antibody, and selects Save

6. Prior to the install of G-GUI v2.7.0, a customer has user-defined protocol variations under –v02 and –v03 with the default set to –v02 for SOX-10 [ZM10] (8308). The customer wants to keep the staining steps in –v02 as their default/MDPV. Which of the following scenarios is the correct upgrade process?(Required)

A) After the G-GUI v2.7.0 upgrade, 8308-v02 was set to MDPV. FAS designates 8308–v01 as MDPV and sets all other protocol variations to approved

B) After the G-GUI v2.7.0 upgrade, 8308-v01 was set to MDPV. In collaboration with the customer, FAS designates 8308–v02 as MDPV and inquires if the customer would like to designate –v03 as non-approved or approved

C) After the G-GUI v2.7.0 upgrade, 8308-v01 was set to MDPV. In collaboration with the customer, FAS designates 8308–v04 as MDPV and inquires if the customer would like to designate –v03 as non-approved or approved

D) After the G-GUI v2.7.0 upgrade, 8308-v01 was set to MDPV. In collaboration with the customer, FAS non-approves the Sakura-provided protocol variations and –v03

7. Which of the following Sakura products contain hazardous material?(Required)

A) SSC Buffer

B) Amplification Linker

C) Proteinase K

D) ISH probes

8. Which of the following Sakura products does not have to be registered or created in the GUI prior to use?(Required)

A) SSC Buffer

B) Amplification Linker

C) Proteinase K

D) ISH probes

9. Which of the following Sakura products must be filled into a user-fillable cartridge?(Required)

A) SSC Buffer

B) Amplification Linker

C) Proteinase K

D) ISH probes

10. Which of the following is not true about ISH?(Required)

A) ISH uses labeled DNA or RNA Probes

B) ISH is used to detect proteins

C) ISH probes must be handled with sterile technique

D) None of the above

Training Quiz: Tissue-Tek Genie® ISH

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