Localization of Odorant Receptor Genes in Locust Antennae by RNA In Situ Hybridization

Podsumowanie

This paper describes a detailed and highly effective RNA in situ hybridization protocol particularly for low-level expressed Odorant Receptor (OR) genes, as well as other genes, in insect antennae using digoxigenin (DIG)-labeled or biotin-labeled probes.

Streszczenie

Insects have evolved sophisticated olfactory reception systems to sense exogenous chemical signals. These chemical signals are transduced by Olfactory Receptor Neurons (ORNs) housed in hair-like structures, called chemosensilla, of the antennae. On the ORNs' membranes, Odorant Receptors (ORs) are believed to be involved in odor coding. Thus, being able to identify genes localized to the ORNs is necessary to recognize OR genes, and provides a fundamental basis for further functional in situ studies. The RNA expression levels of specific ORs in insect antennae are very low, and preserving insect tissue for histology is challenging. Thus, it is difficult to localize an OR to a specific type of sensilla using RNA in situ hybridization. In this paper, a detailed and highly effective RNA in situ hybridization protocol particularly for lowly expressed OR genes of insects, is introduced. In addition, a specific OR gene was identified by conducting double-color fluorescent in situ hybridization experiments using a co-expressing receptor gene, Orco, as a marker.

Wprowadzenie

Insect antennae, which are the most important chemosensory organs, are covered with many hair-like structures – called sensilla – that are innervated by Olfactory Receptor Neurons (ORNs). On the membrane of insect ORNs, Odorant Receptors (ORs), a type of protein containing seven transmembrane domains, are expressed with a coreceptor (ORco) to form a heteromer that functions as an odorant-gated ion channel^1,2,3. Different ORs respond to different combinations of chemical compounds^4,5,6.

Locusts (Locusta migratoria) mainly rely on olfactory cues to trigger important behaviors⁷. Locust ORs are key factors for understanding molecular olfactory mechanisms. Localizing a specific locust OR gene to the neuron of a morphologically specific sensillum type by RNA In Situ Hybridization (RNA ISH) is the first step in exploring the ORs function.

RNA ISH uses a labeled complementary RNA probe to measure and localize a specific RNA sequence in section of tissue, cells or whole mounts in situ, providing insights into physiological processes and disease pathogenesis. Digoxigenin-labeled (DIG-labeled) and biotin-labeled RNA probes have been widely used in RNA hybridization. RNA labeling with digoxigenin-11-UTP or biotin-16-UTP can be prepared by in vitro transcription with SP6 and T7 RNA polymerases. DIG- and biotin-labeled RNA probes have the following advantages: non-radioactive; safe; stable; highly sensitive; highly specific; and easy to produce using PCR and in vitro transcription. DIG- and biotin-labeled RNA probes can be chromogenically and fluorescently detected. DIG-labeled RNA probes can be detected with anti-digoxigenin Alkaline Phosphatase (AP)-conjugated antibodies that can be visualized either with the highly sensitive chemiluminescent substrates nitroblue tetrazolium chloride/5-bromo-4-chloro-3-indolyl-phosphate toluidine salt (NBT/BCIP) using an optical microscope or with 2-hydroxy-3-naphtoic acid-2'-phenylanilide phosphate (HNPP) coupled with 4-chloro-2-methylbenzenediazonium hemi-zinc chloride salt (Fast Red) using a confocal microscope. Biotin-labeled RNA probes can be detected with anti-biotin streptavidin Horse Radish Peroxidase (HRP)-conjugated antibodies that can be visualized with fluorescein-tyramides using a confocal microscope. Thus, double-color fluorescent in situ hybridization can be performed to detect two target genes in one slice using DIG- and biotin-labeled RNA probes.

RNA ISH with DIG- and/or biotin-labeled probes has been successfully used to localize olfactory-related genes, such as OR, ionotropic receptor, odorant-binding protein and sensory neuron membrane protein, in insect antennae of, but not limited to, Drosophila melanogaster, Anopheles gambiae, L. migratoria and the desert locust Schistocera gregaria^{8,9,10,11,12,13,14,15,16}. However, there are two substantial challenges when performing RNA ISH for insect ORs: (1) OR genes (except ORco) are expressed at low levels and only in a few cells, making signal detection very difficult, and (2) preserving insect tissue for histology, such that the morphology is preserved and the background noise is low, can be challenging. In this paper a detailed and effective protocol describing RNA ISH for localizing OR genes in insect antennae is presented, including both chromogenic and Tyramide Signal Amplification (TSA) detection.

Protokół

NOTE: To limit RNA degradation, prepare solutions using wet-autoclaved distilled water (at 121 °C for 60 min) and also wet-autoclave materials.

1. Preparation of RNA ISH Antisense and Sense Probes

1. Target gene amplification and purification
   1. First, produce a 387 bp double-stranded fragment of L. migratoria OR1 (LmigOR1, GenBank: JQ766965) from the plasmid containing the full-length cDNA of LmigOR1 with a Taq DNA Polymerase that adds adenines to both ends of the fragments.
      1. Use a 100 µL final reaction volume, containing 50 µL of 2x reaction mix, 4 µL each of sense and antisense primers (Table 1), 1 µL of plasmid template, and 41 µL of RNase-free H₂O. Use the following PCR protocol: 94 °C for 5 min, followed by 30 cycles of 94 °C for 30 s, 55 °C for 30 s and 72 °C for 1 min, followed by 72 °C for 10 min.
      2. Repeat these steps to produce the 1,303 bp double-stranded fragment of LmigOR2 (GenBank: JQ766966) and 1,251 bp double-stranded fragment of LmigORco (GenBank: JN989549). The primers used in these experiments are presented in Table 1.
      3. Run PCR products on 1.2% agarose gels in 1x Tris-acetate-EDTA buffer and visualize using ethidium bromide staining.
   2. Extract these PCR products using a gel extraction kit.
      1. Following electrophoresis, excise DNA bands from the gel and place the gel slices in a 1.5 mL tube. Then, add 100 µL of binding buffer (Buffer PN) per 0.1 g of gel slice. Vortex and incubate at 50 °C until the gel slice is completely dissolved.
      2. Insert a CA2 adsorption column into the collection tube and add 500 µL of balance buffer (Buffer BL). This improves the absorption capability and stability of the silica membrane. Centrifuge at 12,400 x g for 1 min.
      3. Transfer the dissolved gel mixture to the adsorption column assembly and incubate at room temperature for 2 min. Then, centrifuge tubes at 12,400 x g for 1 min. Discard the flow-through and reinsert the adsorption column into collection tube.
      4. Add 600 µL of wash solution (ethanol added, Buffer PW) twice. Centrifuge at 12,400 x g for 1 min. Discard flow-through and reinsert the adsorption column into collection tube.
      5. Empty the collection tube and recentrifuge the column assembly at 12,400 x g for 2 min to allow evaporation of any residual ethanol.
      6. Carefully transfer adsorption column to a clean 1.5 mL centrifuge tube. Air-dry the pellet for 5-10 min and redissolve the DNA in a suitable volume (e.g., 30 µL) of nuclease-free water.
      7. Incubate at RT for 2 min. Centrifuge at 12,400 x g for 2 min. Discard adsorption column and store the DNA at 4 °C or -20 °C.
2. Construct the recombinant plasmids
   1. Individually ligate the 387 bp fragment of LmigOR1, 1,303 bp fragment of LmigOR2 and 1,251 bp fragment of LmigORco into a T vector that contains promoters for T7 (upstream) and SP6 (downstream) RNA polymerases adjacent to the inserted DNA using T4 DNA ligase. Prepare the following 10 µL reaction: 5 µL of 2x ligation buffer, 1 µL of T vector, 3 µL (∼100 ng) of the inserted gene's DNA and 1 µL of T4 DNA ligase, and incubate O/N at 4 °C.
   2. Add 5 µL of each recombinant plasmid containing the 387 bp fragment of LmigOR1, 1,303 bp fragment of LmigOR2 and 1,251 bp fragment of LmigORco separately into 50 µL of competent Escherichia coli DH5α cells in sterile 1.5 mL tubes.
      1. Mix gently and put the tubes into ice for 30 min and then incubate them for 90 s at 42 °C. Transfer them back into ice for 3 min.
      2. Add 450 µL of Luria-Bertani (LB) liquid medium without ampicillin to every tube and incubate them in a shaker at 150 rpm for 1 h at 37 °C to restore the E. coli DH5α.
      3. Take a 100 µL aliquot of each transformant and use them to inoculate LB solid substrate plates containing 50 µg/mL ampicillin, 24 µg/mL isopropyl β-D-1-thiogalactopyranoside (IPTG), and 40 µg/mL 5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside (X-gal).
      4. Incubate these plates in a constant incubator at 37 °C for 18 h. Screen the target recombinant plasmids using the blue-white screening method. Sequence the target recombinant plasmids using Sanger sequencing and identify the three OR genes' insert directions.
3. Select restriction endonucleases to linearize recombinant plasmids
   1. Use restriction endonucleases that not only digest in the multiple cloning site of the vector but also do not cut the insert DNA. In this experiment, all 3 genes are inserted into the T vector in the direction corresponding to that of the vector.
   2. Use Nco I restriction endonuclease to linearize the recombinant plasmids containing the 387 bp fragment of LmigOR1, 1,303 bp fragment of LmigOR2 and 1,251 bp fragment of LmigORco to produce the antisense probes. Use Spe I restriction endonuclease to produce the sense probes.
      NOTE: If the insert direction corresponds to that of the vector, then a unique restriction site from the end of T7 is selected to linearize the recombinant plasmid and SP6 RNA polymerase is used to prepare the antisense probe. A unique restriction site from the end of SP6 is selected to linearize the recombinant plasmid, and the T7 RNA polymerase is used to prepare the sense probe. Otherwise, if the insert direction does not correspond to the vector's direction, then a unique restriction site from the end of SP6 is selected to linearize the recombinant plasmid and T7 RNA polymerase is used to prepare the antisense probe. The unique restriction site from the end of T7 is selected to linearize the recombinant plasmid, and the SP6 RNA polymerase is used to prepare sense probe.
4. Purifying the linearized recombinant plasmids
   1. Digest 20 µg each of the three recombinant plasmids containing the 387 bp fragment of LmigOR1, 1,303 bp fragment of LmigOR2 and 1,251 bp fragment of LmigORco using the Nco I restriction endonuclease in a 100 µL reaction that contains 10 µL of 10x buffer, 40 µL of 0.5 µg/µL plasmid, 3 µL of Nco I and 47 µL of RNase-free H₂O, followed by a 3 h incubation at 37 °C.
   2. Similarly, digest 20 µg of each of these three recombinant plasmids using the Spe I restriction endonuclease.
   3. Purify these digested plasmids using a gel extraction kit as described in 1.1.2. Determine the concentrations of these extracted linearized recombinant plasmids by spectrophotometry and adjust to 0.5 µg/µL.
5. Prepare antisense and sense probes
   1. Use the T7/SP6 RNA transcription system to generate antisense and sense probes. SP6 RNA polymerase is used to transcribe double-stranded RNA for DIG- and biotin-labeled antisense probes for these three OR genes using linearized recombinant plasmids as templates in vitro. The T7 RNA polymerase is used to produce sense probes. Perform the reaction in a 20 µL final volume, containing 2 µL of 10x NTP mix, 2 µL of 10X transcription buffer, 1 µL of RNase inhibitor, 2 µL of T7 or SP6 RNA polymerase, 4 µL of 0.5 µg/µL linearized plasmid and 9 µL RNase-free H₂O, followed by a 3 h incubation at 37 °C.
   2. Incubate the DIG- and biotin-labeled antisense and sense probes for 30 min with 1 µL DNase at 37 °C. Add 2.5 µL of 5 M LiCl and 75 µL of absolute ethanol, then incubate the reactions for 30 min at -70 °C.
   3. Centrifuge at 15,000 x g for 30 min at 4 °C. Carefully decant the supernatant. Add 150 µL of 70% ethanol to wash the precipitant. Prepare the 70% ethanol (1 L) by adding 95% ethanol (736.8 mL) to sterile distilled water (263.2 mL).
   4. Centrifuge at 15,000 x g for 30 min at 4 °C again and air-dry the pellet for 5-10 min at RT. Add 25 µL of RNase-free H₂O to dissolve the RNA antisense and sense probes.
   5. If the length of the inserted gene is longer than 1 kb, subsequently fragment RNA antisense and sense probes to an average length of ～300 bp by incubation in a bicarbonate-carbonate buffer solutions. Perform the reaction in a 50 µL final volume, containing 25 µL of the RNA probe and 25 µL of the bicarbonate-carbonate buffer solution (80 mM NaHCO₃, 120 mM Na₂CO₃, pH 10.2) at 60 °C. The hydrolysis time required is given by a previously published formula¹⁷.
   6. Add 5 µL of 10% acetic acid to stop the reaction. In this experiment, fragment the LmigOR2 and LmigORco antisense and sense probes for 24 and 23 min, respectively.
      t = (L_o-L_f)/kXL_oXL_f
      L_o= the initial fragment lengths in kb
      L_f=the final fragment lengths in kb
      k=the rate constant for hydrolysis, approximately 0.11 kb^-1min^-1
      t=the hydrolysis time in min
   7. Finally, add 250 µL of hybridization buffer and store at -80 °C.

2. Preparation of Cryostat Sections

1. Precool the freezing microtome to -24 °C.
2. Select new molting adult locusts that are active and have intact antennae. Cut the antennae into 2-3 mm pieces using sterile razors.
3. Put O.C.T. compound on a freezing microtome holder and put one or two samples on the compound horizontally. Then, transfer the holder into the freezing microtome at -24 °C to equilibrate until the compound freezes. Take out the holder and cover the samples with a little compound. Transfer the holder into the freezing microtome at -24 °C again for at least 10 min (Figure 1).
   NOTE: Avoid getting bubbles in the compound.
4. Fix the holder with the samples into the freezing microtome, then section the frozen samples into 12 µm-thick slices at -24 °C.
5. Thaw mount the slices one by one on slides (25  x 75 mm; nuclease-free) and air dry for 10 min.

3. Fixing Sections

1. After preparing cryostat sections, put the slides in a plastic container (～100  x 40  x 80 mm), and fix the tissues by incubating the slides in 4% paraformaldehyde solution (PFA) for 30 min at 4 °C.
2. Wash the slides in 1X Phosphate-Buffered Saline (PBS) for 1 min.
3. To eliminate the alkaline proteins, transfer the slides to 0.2 M HCl for 10 min.
4. To eliminate the surface protein of nucleic acid, transfer the slides to 1XPBS with 1% Triton X-100 for 2 min.
5. Wash the slides twice for 30 s in 1x PBS.
6. Finally, rinse the slides in formamide solution for 10 min at 4 °C.

4. Hybridization

1. Prepare the antisense and sense probes
   1. Use hybridization buffer to dilute RNA antisense or sense probes in the 1.5 mL nuclease-free tubes. In this experiment, for all of the antisense and sense probes (LmigOR1, LmigOR2, and LmigOrco), add 1 µL of probe to 99 µL hybridization buffer per slide. Generally, the use of 1:100 dilutions of antisense probes produces significant positive signals and low backgrounds using this protocol.
   2. For chromogenic detection, dilute DIG-labeled probes individually.
   3. For TSA detection, dilute DIG-labeled LmigOR1 with biotin-labeled LmigOrco probes or DIG-labeled LmigOR2 with biotin-labeled LmigOR1 probes together in the hybridization buffer.
   4. Heat the dilutions for 10 min at 65 °C and put them on ice for at least 5 min.
2. Hybridization
   1. Drain the slides and add 100 µL of diluted antisense and sense probes (Step 4.1) to the tissue sections. Then, place coverslips (24 mm x 50 mm; nuclease-free) on the tissue sections.
   2. Place the covered slides horizontally into a humid box (∼300  x 180  x 50 mm³; Figure 2) and incubate at 55 °C for 22 h. Add formamide solution or 1X PBS to the bottom of the box to keep the environment moist, but do not submerge the slides in the liquid.
3. Washing and blocking.
   1. After hybridization, remove the coverslips carefully. Wash the slides twice for 30 min in 0.1x Saline Sodium Citrate (SSC) at 60 °C.
      NOTE: Washing means putting the slides in a slide holder that is then placed into a plastic container and gently agitated on a rocker (～50 rpm; Figure 2).
   2. Rinse the slides in 1x Tris-Buffered Saline (TBS) for 30 s.
   3. Add 1 mL of 1% blocking reagent in TBS supplemented with 0.03% Triton X-100 on each slide, and incubate for 30 min. Then, discard the blocking solution.
4. Immunohistochemistry.
   1. For chromogenic detection, use blocking reagent in TBS to dilute 750 units (U)/mL anti-digoxigenin AP-conjugated antibody to 1.5 U/mL AP solution. Add 100 µL of AP solution per covered (24 mm x 50 mm) slide.
   2. For TSA detection, use blocking reagent in TBS to dilute 750 U/mL of anti-digoxigenin AP- conjugated antibody and anti-biotin streptavidin HRP- conjugated antibody to the AP/HRP solution. Add 100 µL of AP/HRP solution per covered (24 mm x 50 mm) slide.
   3. Incubate the slides in a humid box (Figure 2) for 60 min at 37 °C. Use the formamide solution or 1X PBS to keep box moist but not soggy.

5. Staining

1. Remove the coverslips carefully. Wash the slides three times for 5 min in 1x TBS supplemented with 0.05% Tween-20. Rinse the slides in DAP-buffer (chromogenic detection: pH 9.5; TSA detection: pH 8.0) for 5 min.
2. Staining (chromogenic detection)
   1. Add 100 µL of NBT (375 µg/mL)/BCIP (188 µg/mL) substrate solution (diluted in DAP; pH 9.5) to every slide. Carefully place coverslips (24 x 50 mm) onto the slides.
   2. Incubate the slides in a humid box with substrate solution for 10 min - O/N at 37 °C.
      NOTE: Check the development by looking at the slides from time to time under the microscope.
   3. When the development is ready, stop the reaction by transferring the slides into water.
3. Staining (TSA detection)
   1. Use a syringe to move the HNPP (100 µg/mL)/Fast Red (250 µg/mL) substrate from the syringe filter (0.22 µm; Figure 2).
   2. Add 100 µL of HNPP/Fast Red substrate per slide covered with a coverslip (24 x 50 mm). Incubate the slides for 30 min with HNPP/Fast Red substrate at RT.
   3. Remove the coverslips carefully, and wash the slides three times for 5 min in 1X TBS supplemented with 0.05% Tween-20.
   4. Use 100 µL of TSA substrate/covered (24 x 50 mm²) slide. Incubate the slides with TSA substrate for 10 min at RT.
   5. Remove the coverslips carefully, and wash the slides three times for 5 min in 1x TBS supplemented with 0.05% Tween-20.
4. Embed the slides in PBS/glycerol (1:3).
   NOTE: After finishing these procedures, the slides should be observed as soon as possible because the fluorescent signal will quench quickly.

6. Observation

1. Chromogenic detection
   1. Observe tissue sections using an optical microscope. Choose the 10X, 20X, and 40X objective lenses to observe the results of chromogenic detection.
   2. Use DP-BSW software to analyze the results and capture the images.
2. TSA detection
   1. Observe tissue sections using a confocal microscope. DIG-labeled genes should be observed under 543 nm light, presenting a red color, and biotin-labeled genes should be observed under 488 nm light, presenting a green color. When they emerge, they present yellow color.
   2. Choose the 20X and 40X objective lenses to observe the results of TSA detection, respectively.
   3. Use FV1000 software to analyze the results and capture the images.

Wyniki

With chromogenic detection, a small subset of the antennal cells in every adult antennal section was denoted by the DIG-labeled LmigOR1 and LmigOR2 antisense probes (Figure 3). RNA ISH on consecutive sections to localize LmigOR1 and LmigOR2 showed that antennal cells expressing the two genes were located in ORN clusters expressing LmigORco, indicating that the putative LmigOR1 and LmigOR2 were act...

Dyskusje

It is hard to perform RNA ISH to localize OR genes in insect antennae because the expression levels of OR genes, except ORco, are very low and preserving histological slices of insect antennae is very difficult. In addition, TSA detection is also very tricky. To address these problems, the following measures should be taken. The antennae are selected from newly molting adult locusts that have thin and soft antennal cuticles, which maintain their morphology on the slide. The frozen samples are sectioned into 12 &...

Materiały

Name	Company	Catalog Number	Comments
Materials
2×TSINGKETM Master Mix	TSINGKE, China	TSE004
RNase-free H2O	TIANGEN, China	RT121-02
REGULAR AGAROSE G-10	BIOWEST, SPAIN	91622
Binding buffer	TIANgel Midi Purification Kit, TIANGEN, China	DP209-02
Balance buffer	TIANgel Midi Purification Kit, TIANGEN, China	DP209-02
Wash solution	TIANgel Midi Purification Kit, TIANGEN, China	DP209-02
T Vector	Promega, USA	A362A
T4 DNA Ligase	Promega, USA	M180A
Escherichia coli DH5α	TIANGEN, China	CB101
Ampicillin	Sigma, USA	A-6140
Isopropyl β-D-1-thiogalactopyranoside	Inalco, USA	1758-1400
5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside	SBS Genetech, China	GX1-500
Nco I	BioLabs, New England	R0193S
Spe I	BioLabs, New England	R0133M
DIG RNA Labeling Kit	Roche, Switzerland	11175025910
Biotin RNA Labeling Kit	Roche, Switzerland	11685597910
DNase	DIG RNA Labeling Kit, Roche, Switzerland	11175025910
LiCl	Sinopharm, China	10012718
Ethanol	Sinopharm, China	10009257
Acetic acid	BEIJING CHEMICAL REGENTS COMPANY, China	10000292
Tissue-Tek O.C.T. Compound	Sakura Finetek Europe, Zoeterwoude, Netherlands	4583
Slides	TINA JIN HAO YANG BIOLOGCAL MANUFACTURE CO., LTE, China	FISH0010
HCl	Sinopharm, China	80070591
Millex	Millipore, USA	SLGP033RS
Tween 20	AMRESCO, USA	0777-500ML
Nitroblue tetrazolium chloride / 5-bromo-4-chloro-3-indolyl-phosphate toluidine salt	Roche, Switzerland	11175041910
Glycerol	Sinopharm, China	10010618
Name	Company	Catalog Number	Comments
Solutions
1×Tris-acetate-EDTA	Sigma, USA	V900483-1KG	0.04mol/L Tris-Base
1×Tris-acetate-EDTA	BEIJING CHEMICAL REGENTS COMPANY, China	10000292	0.12%acetic acid
1×Tris-acetate-EDTA	Sigma, USA	03677	Ethylenediaminetetraacetic acid disodium salt (EDTA)
Luria-Bertani (LB) liquid medium	Sinopharm, China	10019392	10g/L NaCl
Luria-Bertani (LB) liquid medium	MERCK, Germany	VM335231	10g/L Peptone from casein (Tryptone)
Luria-Bertani (LB) liquid medium	MERCK, Germany	VM361526	5g/L Yeast extract
LB solid substrate plate	Sinopharm, China	10019392	10g/L NaCl
LB solid substrate plate	MERCK, Germany	VM335231	10g/L Peptone from casein (Tryptone)
LB solid substrate plate	MERCK, Germany	VM361526	5g/L Yeast extract
LB solid substrate plate	WISENT ING, Canada	800-010-CG	15g/L Agar Bacteriological Grade
10×phosphate buffer saline (pH7.1)	Sinopharm, China	10019392	8.5%NaCl
10×phosphate buffer saline (pH7.1)	Sigma, USA	V900041-500G	14mM KH2PO4
10×phosphate buffer saline (pH7.1)	Sigma, USA	V900268-500G	80mM Na2HPO4
10×Tris buffered saline (pH7.5)	Sigma, USA	V900483-1KG	1M Tris-Base
10×Tris buffered saline (pH7.5)	Sinopharm, China	10019392	1.5M NaCl
Detection Buffer (DAP)       chromogenic detection pH9.5       TSA detection pH8.0	Sigma, USA	V900483-1KG	100mM Tris-Base
Detection Buffer (DAP)       chromogenic detection pH9.5       TSA detection pH8.0	Sinopharm, China	10019392	100mM NaCl
Detection Buffer (DAP)       chromogenic detection pH9.5       TSA detection pH8.0	Sigma, USA	V900020-500G	50mM MgCl2·6H2O
20×saline-sodium citrate (pH7.0)	Sinopharm, China	10019392	3M NaCl
20×saline-sodium citrate (pH7.0)	Sigma, USA	V900095-500G	0.3M Na-Citrate
4% paraformaldehyde solution (pH9.5)	Sigma, USA	V900894-100G	4% paraformaldehyde
4% paraformaldehyde solution (pH9.5)	Sigma, USA	V900182-500G	0.1M NaHCO3
Sodium Carbonate Buffer (pH10.2)	Sigma, USA	V900182-500G	80mM NaHCO3
Sodium Carbonate Buffer (pH10.2)	Sigma, USA	S7795-500G	120mM Na2CO3
Formamide Solution (pH10.2)	MPBIO, USA	FORMD002	50% Deionized Formamide
Formamide Solution (pH10.2)			5×saline-sodium citrate
Blocking Buffer in Tris buffered saline	Roche, Switzerland	11175041910	1% Blot
Blocking Buffer in Tris buffered saline	AMRESCO, USA	0694-500ML	0.03% Triton X-100
Blocking Buffer in Tris buffered saline			1×Tris buffered saline
Alkaline phosphatase solution	Roche, Switzerland	11175041910	1.5 U/ml anti-digoxigenin alkaline phosphatase conjugated antibody
Alkaline phosphatase solution			Blocking Buffer in Tris buffered saline
Alkaline phosphatase/ horse radish peroxidase solution	Roche, Switzerland	11175041910	1.5 U/ml anti-digoxigenin alkaline phosphatase conjugated antibody
Alkaline phosphatase/ horse radish peroxidase solution	TSA kit, Perkin Elmer, USA	NEL701A001KT	1% anti-biotin streptavidin horse radish peroxidase- conjugated antibody
Alkaline phosphatase/ horse radish peroxidase solution			Blocking Buffer in Tris buffered saline
Hybridization Buffer	MPBIO, USA	FORMD002	50% Deionized Formamide
Hybridization Buffer			2×saline-sodium citrate
Hybridization Buffer	Sigma, USA	D8906-50G	10% dextran sulphate
Hybridization Buffer	invitrogen, USA	AM7119	20 µg/ml yeast t-RNA
Hybridization Buffer	Sigma, USA	D3159-10G	0.2 mg/ml herring sperm DNA
2-hydroxy-3-naphtoic acid-2'-phenylanilide phosphate/ 4-chloro-2-methylbenzenediazonium hemi-zinc chloride salt substrate	Roche, Switzerland	11758888001	1% 2-hydroxy-3-naphtoic acid-2'-phenylanilide phosphate (10mg/ml)
2-hydroxy-3-naphtoic acid-2'-phenylanilide phosphate/ 4-chloro-2-methylbenzenediazonium hemi-zinc chloride salt substrate	Roche, Switzerland	11758888001	1% 4-chloro-2-methylbenzenediazonium hemi-zinc chloride salt (25mg/ml)
2-hydroxy-3-naphtoic acid-2'-phenylanilide phosphate/ 4-chloro-2-methylbenzenediazonium hemi-zinc chloride salt substrate			Detection Buffer
Tyramide signal amplification substrate	TSA kit, Perkin Elmer, USA	NEL701A001KT	2% fluorescein-tyramides
Tyramide signal amplification substrate	TSA kit, Perkin Elmer, USA	NEL701A001KT	Amplification Diluent
Name	Company	Catalog Number	Comments
Instrument
Freezing microtome	Leica, Nussloch, Germany	Jung CM300 cryostat
Spectrophotometer	Thermo SCIENTIFIC, USA	NANODROP 2000
Optical microscope	Olympus, Tokyo, Japan	Olympus IX71microscope
Confocal microscope	Olympus, Tokyo, Japan	Olympus BX45 confocal microscope