96-well RNA In Situ Hybridization Protocol
M13 (-21) 5' TGTAAAACGACGGCCAGT 3'
M13 (REV) 5' GGAAACAGCTATGACCATG 3'
PM001a 5' GTCGACGTTAGAACGCGGCTAC 3'
PM002a 5' GGGTTAAATTCCCGGGTACTGC 3'
SK-30 5' GGGTAACGCCAGGGTTTTCC 3'
SKMet 5' ATGACCATGATTACGCCAAGC 3'4. DNA Polymerase (DyNAzyme EXT DNA Polymerase-MJ Research, store at -20°C). 5. Inoculated cells (can be stored for up to 7 days at 4 ° C). 6. Multichannel pipette (Brand). 7. GeneAmp PCR System 9700 (Applied Biosystems). 8. Speedball roller (E&K Scientific). 9. Aluminum plate sealers (Polarseal:Foil adhesive Tape for multiwell plates T592100) (E&K Scientific) or 8-strip PCR caps (E&K Scientific). **1.1.3.** **PCR Product Purification (G-50 column chromatography)** 1. Sephadex ™G-50 Superfine (Amersham Pharmacia Biotech). 2. MultiScreen column loader-45 µl (Milliore) MAHV N45 filter plate (Millipore). 3. MultiScreen Centrifuge Alignment Frame (Millipore). 4. Multichannel pipette (Brand). 5. Sterile 0.1% diethyl pyrocarbonate (DEPC, Sigma, handle carefully, toxic) treated H20 (autoclaved). 6. Eppendorf Centrifuge 5810 (equipped with 96-well plate holders). 7. 96-well semi-skirt PCR plate (E&K Scientific). 9. Aluminum plate sealers or 8-strip PCR caps (E&K Scientific). **1.1.4.** **RNA Probe Preparation** 1. 96-well semi-skirt PCR plate (E&K Scientific). 2. Multichannel pipette (Brand). 3. Speedball roller (E&K Scientific). 4. GeneAmp PCR System 9700 (Applied Biosystems). 5. Aluminum plate sealers or 8-strip PCR caps (E&K Scientific). 6. Eppendorf Centrifuge 5810 (equipped with 96-well plate holders). 7. 2X Polymerase mix (2U \[T7, T3, Sp6\] RNA polymerase (Roche, store at -20°C), 4.6U RNase inhibitor (Amersham Parmacia Biotech), 10mM NTPs (Roche, store at -20°C), 3.5mM digoxigenin-11-UTP (Roche, store at -20°C), 40mM Tris pH 8.0, 6mM MgCl2, 10mM DTT and 2mM spermidine). 8. DEPC treated H20 (22.214.171.124). 9. 0.2 M Tris pH 8 (Dissolve 121.1 gms Tris-base in water, adjust pH with concentrated HCl; pH of Tris is temperature sensitive, sterilize by autoclaving). 10. 10X DNaseI Buffer (0.2 M Tris pH 8, 0.1 M MgCl2. 11. DNaseI mix (1U DNaseI (Amersham Pharmacia Biotech) (RNase-free, store at -20°C), 20 mM Tris pH 8, 10 mM MgCl2,, 10mm DTT). 12. 1 M Dithiothreitol (DTT) (Sigma) (Dissolve 3.09 g of DTT in 20 ml of 0.01 M sodium acetate pH 5.2, sterilize by filtration, aliquot and store at -20°C). 13. 0.2M Na2CO3 pH 10.2 14. 7.5M NH4OAC. 15. Absolute ethanol. 16. Resuspension buffer (50% formamide, 5mM Tris-HCl pH 7.5, 0.5mM EDTA and 0.01% Tween 20). 17. Formamide (Sigma). 18. TE pH 7.5 (10 mM Tris-HCl pH 7.5, 1 mM EDTA). 19. Tween 20 (polyoxyethykenesorbitan monolaurate) (Sigma). 20. Aluminum plate sealers or 8-strip PCR caps (E&K Scientific). **1.1.5.** **RNA Probe Quantificaton** 1. DIG Quantification Teststrips (Roche). 2. DIG Control Teststrips (Roche). 3. 300 µl/well 96-well plate (E&K Scientific). 4. Multichannel pipette (Brand). 5. Falcon Pipetaid. 6. Aluminum plate sealers or 8-strip PCR caps (E&K Scientific). 7. Positively charged Nylon membrane (Roche). 8. UV Stratlinker (Stratagene). 9. HybAid tubes (HybAid Limited). 10. HybAid Hybridization oven (HybAid Limited). 11. 1X blocking solution (Dissolve 10 g of blocking reagent (Roche) in 0.1M maleic acid, 0.15M NaCl adjust pH to 7.5 with NaOH (solid), store at 4 ° C). 12. Tween 20 (polyoxyethykenesorbitan monolaurate, Sigma). 13. Anti-Digoxigenin-AP Fab Fragments (Roche). 14. AP Buffer (0.1M NaCl, 0.05M MgCl2, 0.1M Tris pH 9.5, 0.1% Tween 20; prepare fresh before use). 15. Developing solution (Roche, 45 µl NBT and 35 µl BCIP, store at -20°C) per 10 ml of AP Buffer; add NBT/BCIP just before use). **1.2.** **96- well Plate RNA *in situ*** Hybridization **1.2.1.** **Embryo Collection** 1. Foam Trays (Xpedex). 2. Fly Food1 (3500 ml H2O, 125 g Agar, 125 g Sucrose, 8 g p-Hydroxybenzoic Acid Methyl Ester, 1360 ml Grape Juice, 100 ml 1.25 N NaOH). 3. Yeast (Fleishman) - Mix yeast with H20 to form a thick paste. **1.2.2.** **Embryo Fixation** 1. Three-level sieve (nominal sieve openings (850 µm (20), 250 µm (60), 150µm (100)) (Fisher). 2. Falcon Pipetaid. 3. Paint brush (Winsor & Newton). 4. Crystallization dish (Fisher). 5. 100% sodium hypochlorite (commercial bleach, Kem Tek). 6. GyrotoryÂ¨ shaker Model G2 (New Brunswick). 7. Heptane (Fisher). 8. Formaldehyde (Sigma, ACS reagent grade, 25 ml aliquots). 9. DEPC treated H20 (126.96.36.199). 10. PBS (Dissolve 8 g of NaCl, 0.2 g KCl, 0.24 g KH2PO4 and 2.72 g Na2HPO4 ·7H20 in 800 ml of DEPC treated H20, adjust pH to 7.4 with HCl, adjust volume to 1L, sterilize by autoclaving). 11. Methanol (EM Science). **1.2.3.** **96- well Plate RNA *in situ*** Hybridization 1. Master Embryo Mix (see section 188.8.131.52 note 26). 2. RNA Probe (see section 3.1.4). 3. Genetix Q-Fill 2 plate filler. 4. Millipore MAVM 096 01 vacuum manifold. 5. 300µ l/well 96-well plate (E&K Scientific). 6. Speedball roller (E&K Scientific). 7. Model 1545 Incubator (VWR). 8. Formaldehyde (Sigma). 9. DEPC treated H20 (184.108.40.206). 10. PBS (Dissolve 8 g of NaCl, 0.2 g KCl, 0.24 g KH2PO4 and 2.72 g Na2HPO4 ·7 H20 in 800 ml of DEPC treated H20, adjust pH to 7.4 with HCl, adjust volume to 1L, sterilize by autoclaving). 11. Tween 20 (polyoxyethykenesorbitan monolaurate, Sigma). 12. Methanol (EM Science). 13. PBT (0.1% Tween 20 in PBS). 14. 20X SSC (Dissolve 175.3 g NaCl and 88.2 g of Sodium Citrate in 800 ml of DEPC treated H20, adjust pH to 7, adjust volume to 1L, sterilize by autoclaving). 15. Hybridization buffer (50% formamide, 4X SSC, and 0.01% Tween 20, store in the dark at -20 °C). 16. Clay AdamsÂ¨ Brand Nutator. 17. 50% Dextran Sulfate (Dissolve 25 g of dextran sulfate in DEPC H20, adjust volume to 50 ml). 18. Hybridization Buffer with dextran sulfate, (50% formamide, 4X SSC, 5%dextran sulfate and 0.01% Tween 20 store in the dark at -20 °C). 19. GyrotoryÂ¨ shaker Model G2 (New Brunswick). 20. Wide opening pipete tips (Rainin). 21. 25 ml reagent reservoir (Matrix). 22. 96-well filter plate (Millipore MADV N65) 23. Wash buffer (50% formamide, 2X SSC and 0.01% Tween 20; prepare fresh before use). 24. Goat Serum (Roche, store at -20°C). 25. Anti-Digoxigenin-AP Fab Fragments (store at 4 ° C) (Roche). 26. AP Buffer (0.1M NaCl, 0.05M MgCl2, 0.1M Tris pH 9.5, 0.1% Tween 20; prepare fresh before use). 27. Developing solution (Roche, 45 µl NBT and 35 µl BCIP, store at -20°C, per 10 ml of AP Buffer; add NBT/BCIP just before use). 28. Absolute ethanol. 29. 70% Glycerol (Sigma, 70:30 Glycerol:PBS, filter sterilize). 30. Aluminum plate sealers (E&K Scientific). 31. Low magnification microscope (Zeiss-Stemi 2000-C). 2. Methods **2.1.** **Probe Preparation** **2.1.1.** **Cell Inoculation** 1. Add 176 µl of 50 mg/ml Carbenicillin to 110 ml of SB and mix thoroughly2. 2. Add 1.0 ml of Carbenicillin /SB mix into each well of a 96-well Ritter Riplate using a multichannel pipette. 3. Add 10 µl of thawed cells per well using a multichannel pipette (Brand). 4. Seal tightly with Airpore Tape Sheets. 5. Place Ritter Riplate in a 37 ° C shaking incubator set at 300 RPM for 18 hrs. 6. Store at 4 ° C. 7. Cells are now ready for PCR. **2.1.2.** **PCR** 1. Dilute cells 1:100 in sterile deionized H20. 2. For one 96-well PCR prepare a total of 3.19 ml reaction mix (enough for 110 reactions) containing 1X PCR buffer (supplied with DyNAzyme EXT DNA Polymerase-MJ Research), 200 µM dNTPs, 0.3 µM primers and 22 U DNA polymerase. 3. Add 29 µl of the mix to each well using a multichannel pipette. 4. Add 1 µl 1:100 cell dilution into each well using a multichannel pipette, mix thoroughly and centrifuge at 4000 rpm for one minute. 5. Place plate in PCR machine.
Cycling Conditions for amplification of clones in pFLC-I:
94 ° C 1min__________
94 ° C 30sec
66° -2 °C 45sec 5 Cycles
72 °C 3min+12sec_____
94 ° C 30sec
56 ° C 45sec 30 Cycles
72 °C 3min+6sec______
72 °C 15min__________
4 °C ∞
Cycling Conditions for amplification of clones in pOT2A:
94 ° C 1min__________
94 ° C 30sec
67 °-1 °C 45sec 5 Cycles
68 °C 3min _____
94 ° C 1 min
62 ° C 45sec 32 Cycles
68 ° C 4min+6sec______
68 ° C 10min__________
4 °C ∞
Cycling Conditions for amplification of clones in pBS:
95 ° C 1min__________
95 °C 30sec
70 °-2 °C 45sec 5 Cycles
72 °C 3min+12sec_____
95 °C 30sec
60 °C 45sec 28 Cycles
72 °C 3min+6sec______
72 °C 15min__________
4 ° C ∞6. To monitor the PCR reaction, samples are quantitated and sized by electrophoresis through 1% agarose in TAE (40 mM Tris, 20 mM acetate, 2mM EDTA, pH 8.1) using either the centipede (96 samples) or millipede (192 samples) electrophoresis apparatus (Owl Scientific). 7. The samples are now ready for G-50 purification. **2.1.3.** **PCR Product Purification (G-50 column chromatography)** 1. Use MultiScreen column loader to measure out the proper amount of G-50 powder. 2. Fit a filter plate snugly on top of the MultiScreen column loader and turn upside down to transfer the powder. 3. Hydrate your G-50 plate with 300 µl of DEPC treated H20 per well and let sit at least 3 hrs, but not more than 24 hrs.3 4. 25 µl of PCR product per well plate are ready for transfer. 5. To prepare the G-50 filtration plate, place the already hydrated G-50 plate on top of a 96-well plate with alignment frame fitted on top of it. Centrifuge plates at 910 rpm for 5 min. (This will remove excess water from the G-50 plate). 6. Transfer PCR product into the prepared G-50 filtration plate. 7. Place the G50 filtration plate on top of the labeled 96-well semi-skirt PCR plate. 8. Centrifuge the G50 filtration plate with your product at 910 rpm for 5 min. 9. The samples are now ready for probe preparation. **2.1.4.** **RNA Probe Preparation** 1. Put 5 µl of 2x polymerase mix into each well of 96-well plate using a multichannel pipette. 2. Add 5 µl of PCR product using a multichannel pipette. 3. Incubate in a PCR machine at 37 °C for 2 hrs. 4. Add 10 µl of DNase I mix into each well using a multichannel pipette. 5. Incubate in a PCR machine at 37 °C for 15 min. 6. Add 20 µl of 0.2M Na2CO3 pH 10.2 to each well using a multichannel pipette. 7. Incubate at 60 °C in a PCR machine for 15 min. 8. Place plate on ice and quickly add 20 µl of 7.5M NH4OAc into each well using a multichannel pipette. 9. Add 160 µl of ethanol, seal well4, vortex to mix and centrifuge at 4000 rpm for one minute. 10. Incubate at room temperature for 10 min. 11. Centrifuge at 4000 rpm for 30 min at room temperature. 12. Drain by inverting plate 6X, centrifuge at 800 rpm with plate upside down to drain remaining liquid. 13. Quickly resuspend in 50 µl of resuspension buffer5. 14. Vortex at maximum speed for 25 sec and centrifuge at 4000 rpm for one minute. 15. Store at -80 °C). 16. The RNA probe is now ready to be quantified. **2.1.5.** **RNA Probe Quantification**
Using multichannel pipette spot 1 µl of resuspended RNA probe onto a positively charged nylon membrane6.
Using a multichannel pipette spot 1 µl of controls7 onto the same nylon membrane.
Crosslink in UV Stratalinker (use the autocrosslink function for steps 3 -10 use hybaid hybridization oven and tube*).*
Wash 2X with blocking solution for 5 minutes.
Incubate in blocking solution at room temperature for 30 minutes.
Incubate in a solution of 1:2000 dilution of Anti-Digoxigenin-AP Fab Fragment in blocking solution at room temperature for 30 minutes.
Wash 4X with blocking solution for 15 min.
Wash 2X with AP buffer for 5 min.
Develop color in the dark8 with developing solution9 (about 20 min).
Wash 3X in blocking solution to stop the color reaction for 3 min each.
Compare the RNA probes with controls (3, 10, 30, 100 and 300 pg) and determine the success rate10.
RNA probe is now ready to be used in hybridization.
Keep embryos of different time periods separate during fixation1. Collect embryos from food tray by rinsing the tray with deionized water and capturing the embryos in the three level sieve. The sieving removes fly food and yeast paste17. 2. Fill reservoir18 with 100% bleach and shake embryos for 3 min.19 to remove the chorion membrane. 3. Wash well with distilled water. 4. Remove embryos form the sieve using a spatula and place in a 50ml falcon tube. Fix embryos by gently shaking in 50-50 mix of heptane20 and 4% formaldehyde/PBS21 fixative for 25 min. 5. Remove *lower* aqueous phase and replace with equal volume of methanol. 6. Shake for 1 min then allow embryos to settle. **DO NOT VORTEX**. 7. Remove *upper* phase22 containing the vitelline membranes and embryos remaining at interphase23. 8. Remove remaining methanol24. 9. Wash 3x in methanol. 10. Top off 50ml Falcon tube with methanol. 11. Store embryos at -20 °C25. 12. Embryos are now ready to be hybridized. **2.2.3.** **96-well Plate RNA *in situ*** Hybridization 1. Prepare a master embryo mix by combining equal amounts of embryos from all six time periods in a 50 ml Falcon tube26. 2. Use 1ml of embryos from the master mix per 96-well plate and place them in a 15 ml Falcon tube. 3. Rehydrate in 3:1 methanol:2.5% formaldehyde in 1X PBS27,\ 28 for 2 min. 4. Rehydrate in 1:3 methanol:2.5% formaldehyde in 1X PBS29 for 5 min. 5. Post-fix in 2.5% formaldehyde in 1X PBS for 10 min 30. *6.* Rinse 6x in PBT. 7. Add 3 ml of hybridization buffer without dextran sulfate per 1 ml of embryos31 8. Incubate with shaking at 125 rpm on the GyrotoryÂ¨ shaker for at least 1 hr at room temperature to pre-hybridize embryos. 9. During pre-hybridization put 200 µl of hybridization buffer with dextran sulfate into each well of a 96-well plate using multichannel pipette. 10. Add 2 µl of probe into each well in columns 1-11. Add 2 µl of control probe into wells in column 12. (Use one well in column 12 for a negative control and do not add probe). 11. Mix thoroughly on a vortex mixer at maximum speed for 25 sec and centrifuge at 4000 rpm for one minute. 12. Carefully pour pre-hybridized embryos into a 25 ml reagent reservoir. 13. Add 20 µl of embryos into each well of a 96-well filter plate (using a multichannel pipette with wide opening tips) 32. 14. Transfer the probes from the 96-well plate into the 96-well filter plate and seal the filter plate with an aluminum foil sealer. 15. Incubate at 55 °C with shaking at 125 rpm on the GyrotoryÂ¨ shaker overnight 33. 16. Add 100 µl of room temperature wash buffer. 17. Remove the hybridization-buffer, wash-buffer mix using vacuum; once all the liquid is removed from the wells *quickly* turn off the vacuum34. 18. Rinse 2x with wash buffer. 19. Incubate in wash buffer at 55 ° C with shaking for 30 min with eight changes. 20. Incubate in wash buffer at 55 °C with shaking overnight. 21. Rinse in PBT. 22. Incubate in PBT at RT with shaking for 30 min; remove PBT. 23. Incubate in PBT, 5% goat serum, 1:2000 dilution Anti-Digoxigenin-AP Fab Fragments at RT with shaking for 2 hrs. 24. Rinse 2x with PBT. 25. Incubate in PBT at RT with shaking 9 X for 10 min each. 26. Rinse 2x with AP buffer. 27. Wash in AP buffer at RT for 5 min; remove AP buffer. 28. Add developing solution (section 220.127.116.11) 29. Incubate with shaking until desired color development is achieved (about 75 min); remove developing solution by vacuum aspiration. 30. Rinse 3x in PBT to stop the color reaction. 31. Rinse 6x in ethanol. 32. Rinse in PBT. 33. Add 70% glycerol. 34. Store at 4 ° C35. 35. Check individual wells on the plate under a low power magnification microscope36. 36. Embryos are ready to be photographed. 3. Notes
1. Add agar into the water and bring to boil while mixing continuously. Wait for agar to go into solution. Add base before adding grape juice. Add remaining ingredients. Mix thoroughly. Use a beaker with handles to pour hot fly food onto the prepared trays. Let the food cool to room temperature before storing at 4 ° C.
2. For each step prepare enough reaction mix for 110 reactions per plate.
3. Hydrate G-50 plate while running the PCR to save time.
4. Individual wells are very full and if the plate is not properly sealed contamination can occur. It is best to use 8-strip PCR caps rather than aluminum plate sealers to prevent cross-contamination.
5. Resuspension buffer waste must be discarded into properly labeled Formamide waste container.
6. The nylon membranes must not overlay each other to ensure proper contact with the antibody solution. Therefore, if using more than one nylon membrane per tube, the length of individual membrane sheets should be no more that 11 cm.
7. Preparation of Controls. Spot 1 µl of each of 5 dilutions (1:3.3, 1:10, 1:33, 1:100, and 1:330) of several different probes onto DIG Quantification Teststrips. Take the loaded DIG Quantification Teststrips and a DIG Control Teststrip through the quantification procedure. Evaluate which of the probe dilution series best approaches the control teststrip. Prepare an adequate amount of this probe dilution series and store at -80°C for future use.
8. Cover the Hybaid oven door with aluminum foil. Keep the developed nylon membranes in the dark even after stopping the color reaction, otherwise they will turn completely blue over time.
9. Developing solution must be discarded into a properly labeled NBT/BCIP waste container.
10. If the probe spot is at least as intense as the 1:330 control spot the RNA probe reaction was successful and the RNA probe is ready to be used in hybridization.
11. Flies lay better in the dark. Keep the fly cages in a room without windows or cover cages with a light-tight dark cloth.
12. For maximum egg deposition make sure the fly food trays and yeast paste are at room temperature before placing in the fly cage.
13. The paste has to be easily spreadable, so that the fly food will not separate from the tray, but not too watery so that the flies will not stick to the paste.
14. Hybridization assays are conducted usingstaged embryos from 0 to 18 hrs post fertilization. Due to uneven egg deposition during this period, embryos are collected in 3 hr intervals (0-3, 3-6, 6-9, 9-12, 12-15, 15-18) to ensure equal representation of all developmental stages in the master mix made by combining equal amounts of embryos from each 3 hr interval.
15. Example of Embryo Collection Schedule
|Week 1&2||Week 1||Week 2|
** Embryos from Cage #2 are fixed at three different times depending on the desired interval (0-3, 3-6 at 1:30 pm same day as collected; 6-9,9-12 at 7:30 pm same day as collected; 12-15, 15-18 at 7:30 am the day after collection).
16. Carefully remove any flies that may have stuck to the fly food or the yeast paste to prevent further egg deposition. While removing the flies take care not to damage the deposited embryos.
17. Pour enough deionized H20 on the tray to cover the entire area. Use paintbrush to collect the embryos from the tray and carefully pour them into the prepared three level sieve. The first sieve (20) will collect pieces of loose agar, the second sieve(40) will collect loose fly parts (e.g. abdomens, wings and heads) and the third sieve will collect the clean embryos.
18. Must be large enough to contain one level of the sieve and high enough so that the embryos in the sieve are can be submerged in liquid. (e.g. 100% bleach, deionized H20).
19. Timing of this step is critical. If the embryos are left in bleach for too long they will be irreparably damaged.
20. Heptane must be discarded into a properly labeled heptane waste container.
21. Formaldehyde/PBS mixture must be prepared fresh just prior to use. Formaldehyde is a classified as a human carcinogen and should be handled with caution and discarded into a properly labeled Formaldehyde waste container.
22. When removing the upper (heptane) phase, start at the interphase and work your way up. Use Falcon Pipetaid.
23. Good embryos, unbroken embryos devoid of chorion and vitelline membranes, will sink to the bottom. Embryos remaining at interphase are damaged and should not be used in hybridization.
24. Methanol must be discarded into a properly labeled methanol waste container.
25. Do not put more than 7 ml of embryos in a 50 ml falcon tube. Lay the falcon tube on its side to prevent crushing the embryos.
26. The embryo master mix is created by combining equal volumes of embryos of all collected stages. It is best to measure out the individual stages in an eppendorf tube and then transfer individual time intervals into a prepared falcon tube. Let the embryos settle to ensure equal volumes. Easiest way to transfer the embryos is by turning the eppendorf tube upside down above the falcon tube and washing out the embryos with methanol using the pipetaid.
27. Waste from steps 3,4 and 5 of the hybridization protocol (3.2.3) must be discarded into a properly labeled Formaldehyde waste container.
28. Use 12ml total (9ml methanol, 2.88ml PBS, 120ul formaldehyde)-prepare fresh just before starting the hybridization steps.
29. Use 12ml total (3ml methanol, 8.64ml PBS, 360ul formaldehyde)- prepare fresh just before starting the hybridization steps.
30. Use 12ml total (11.52ml PBS, 480ul formaldehyde)- prepare fresh just before starting the hybridization steps.
31. Hybridization buffer with and without dextran sulfate and wash buffer must be discarded into a properly labeled Formamide waste container.
32. Even though there is no way to add exactly the same amount of embryos into each well, care needs to be taken to get as close as possible. If the difference in the numbers of embryos between individual wells is too large, the wells with fewer embryos will drain more quickly than the wells with greater numbers of embryos. The embryos in the wells with fewer number will get flattened and stick together. As a result, the morphology of these will be compromised.
33. For steps 15-31 use the Q-Fill to fill the filter plates (except in steps 22&27, for these use the Electrapette 1550) and use the vacuum manifold to remove the liquid. All volumes are 200 µl per well unless otherwise specified.
34. Set the vacuum on the lowest setting to prevent embryos from getting flattened, crushed or stuck to the membrane.
35. Seal the top of the plate with an aluminum plate sealer using the speedball roller. Then carefully seal the bottom of the plate with another aluminum plate sealer. Place the roller on the bench upside down and slide the bottom of the place on in it until a good seal is formed. This is to prevent the glycerol from leaking out of the filter plate.
36. Check individual wells to make sure that the embryos on the plate as a whole are of high quality--that the controls worked properly, that the hybridization signal quality is high (no or minimal background) and that the embryo morphology is good (e.g. embryos are not broken, flattened nor squashed).
This page last updated on: 1/20/05