Re: [Histonet] Need assistance with in situ protocol!!! (LONG)
Would recommend running the following controls:
1. Slide with no sense probe (but all the other reagents)
2. Slide with no probe, no antibody
If Slide 1 and 2 shows staining then you have endogenous AP activity, this
is extremely unlikely with all the pretreatment that you do (prot K,
acetic anhydride, etc).
If only Slide 1 shows staining then the antibody is binding
non-specifically to the tissue (again unlikely, but it is better to rule
out the possibility). If you do see staining here then the antibody might
need to be pre-adsorbed with mouse kidney tissue materials.
If both the above slides are negative then the next step would be to
titrate the probe concentration and the hybridization and
Simplest would be to run a set of slides with 1/3rd and 1/10th the amount
of sense and anti-sense probes and see if the signal intensity decreases
with probe concentration. In addition you might need to increase
stringency (higher wash temperature) to maximize the difference between
sense and anti-sense probes.
If none of the above work, then back to the drawing board and re-design
the probes (were they checked by BLASTing the Sequences?).
Sent by: email@example.com
12/17/2004 07:21 AM
[Histonet] Need assistance with in situ protocol!!! (LONG)
I am in dire need of having my in situ protocol work!! I cannot find the
problem and feel there may be too many to fix the situation on my own.
Please if you are up for the challenge, look over my protocol and problems
I am facing and offer up any suggestions or changes I should make. Also,
does anyone know of a good DIG-labeled RNA probe that a particular
manufacturer makes and that can be used for targets found throughout
different mouse tissues -- just trying also to ensure protocol is wrong
and not probe??
Note: Letter ?u? used to represent micro. Temps given in celcius.
Sorry ? can?t tell you what probe I was using. Only that it is a
DIG-labeled RNA probe.
Antisense and sense appear to both stain.
Large amount of background (endogenous peroxidase?)
At the end of my washes (after hybridization) tissue begins to
disintegrate and cells begin falling away from the sections in large
clumps ? only tissue I am using is mouse kidney. The kidney is perfused
(saline then 4% PF/PBS ? RNase free) and allowed to sit overnight in 4%
PF/PBS. Afer switching the 70% alcohol for ~3-5 hours, the tissues are
routinely processed and embedded.
Sections are sectioned ? 5 um, and placed onto positively charged barrier
slides (Biogenex). They incubate on a plate (covered) at 37 degrees and
then before deparaffinizing are baked at 55 degrees for 1 hour.
At all times RNase free glassware/solutions are used during the entire
process. Bench tops and surrounding area wiped with RNase Away.
Slides deparaffinized and brought down to distilled water, then washed 2x
(5mins each) in 1x PBS.
Proteinase K digestion:
Slides incubated in 0.1M Tris and 50mM EDTA (pH 8) prewarmed at 37
degrees containing 5 ug/ml Prot. K. Incubation time 17mins (determined to
After incubation, slides immersed in 0.1M glycine/PBS for 5 mins.
The slides were then post-fixed in 4% paraformaldehyde/PBS for 3 mins. Rm
Rinse with 1x PBS 2x (5 mins)
Slides placed in a glass staining jar containing 0.1M triethanolamine and
while stirring, acetic anhydride was added to a final concentration of
0.25% acetic anhydride.
Slides rinse in distilled water and then dried on hot plate (37-40
degrees) for ~10-15 mins.
Buffer: Frozen at ?20 degrees. Placed in 50 degree waterbath before use.
Reagents Final Concentration
Deionized formamide 50%
20x SSC 5x
Dextran sulfate 10%
100x denhardt?s solution 5x
10% SDS 2%
10mg/ml denatured 100ug/ml
sheared salmon DNA
Aliquots of 900ul made up and frozen.
Dilute riboprobe in buffer to final concentration of 2.5ng/ul ( DIG-label
To each section between 40-60 ul of probe was added to cover section ?
more for larger sections.
Sections placed in hybridization chamber (Boekel) at 42 degrees, covered
each section with Parafilm to avoid evaporation.
Slides incubated at above temp. 20 hours overnight. Chamber kept humid
with 5x SSC in the provided wells.
Checked slides next day to ensure moisture still under parafilm and that
there was no evaporation ? none seen.
Slides placed in 2x SSC/0.1%SDS for 2mins. Parafilm begins to float off
to liquid surface.
Slides washed in 2x SSC/0.1% SDS at room temp shaking gently 2x (5 mins
Wash slides 0.1x SSC/0.1%SDS at the same temperature used for
hybridization (prewarmed at 42 degrees) -- 2x 10mins each
Rinsed briefly in 2x SSC twice (Room Temp) to remove traces of SDS
Slides incubated with 10ug/ml RNase solution in 2x SSC at 37 degrees for
to selectively degrade single stranded RNA and reduce non-specific signal.
Wash in 2x SSC/ 50%formamide for ½ hr. at 52 degrees gently shaking
Rinse briefly in 2x SSC Rm. temp.
Placed into Buffer 1:
80ml 1 M Tris-HCl pH 7.5
40ml 3M NaCl
Add autoclaved deionized water to 800ml
Place into fresh Buffer 1 for 5 mins.
Place into Buffer 2 for 30 mins. shaking Rm. Temp.
1 M Tris HCl pH 7.5
Triton X-100 (0.5%)
10% Blocking Reagent (1% final concentration)
Blocking reagent bought from Roche (final concentration is 1% or 1x)
Blocking Reagent Cat. No. 1 096 176 ? made up as instructed by
Sheep Anti-DIG-AP antibody used (Roche) ?0- Cat. No. 1 093 274
Buffer 2 tapped off and 100-150ul of antibody, diluted 1:50 in 6ml 2%
normal sheep serum/0.5% Triton X-100 in PBS was added.
Slides incubated with antibody at 37 degrees for 2 hours.
Slides washed 3x in PBS (5 mins. each)
Rinsed in 100mM Tris-HCl (pH 9.5)
In darkness make up BCIP/NBT solution while rinsing in above Tris.
BCIP/NBT provided by DAKO ? new kit, made up as specified. Difficult to
make mistake here.
Added BCIP/NBT solution 3-4 drops to cover section. After 20-30 mins.
Slides checked for signal.
Little seen except for tissue coming off slides (clumps of cells) and
Allowed to sit overnight at 4 degrees ? next day there was signal ? very
strong in some slides ? however, there was background, and sense and
antisense slides had what appeared to be signal.
??? Any suggestions???
THANK YOU FOR YOUR ASSISTANCE
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