Generation of Transgenic Rats using a Lentiviral Vector Approach

Summary

This article aims to provide the methodology for lentiviral transgenesis in rat embryos using multiple injections of a virus suspension into the zygote perivitelline space. Female rats that are mated with a fertile male strain with a different dominant fur color is used to generate pseudopregnant foster mothers.

Abstract

Transgenic animal models are fundamentally important for modern biomedical research. The incorporation of foreign genes into early mouse or rat embryos is an invaluable tool for gene function analysis in living organisms. The standard transgenesis method is based on microinjecting foreign DNA fragments into a pronucleus of a fertilized oocyte. This technique is widely used in mice but remains relatively inefficient and technically demanding in other animal species. The transgene can also be introduced into one-cell-stage embryos via lentiviral infection, providing an effective alternative to standard pronuclear injections, especially in species or strains with a more challenging embryo structure. In this approach, a suspension that contains lentiviral vectors is injected into the perivitelline space of a fertilized rat embryo, which is technically less demanding and has a higher success rate. Lentiviral vectors were shown to efficiently incorporate the transgene into the genome to determine the generation of stable transgenic lines. Despite some limitations (e.g., Biosafety Level 2 requirements, DNA fragment size limits), lentiviral transgenesis is a rapid and efficient transgenesis method. Additionally, using female rats that are mated with a fertile male strain with a different dominant fur color is presented as an alternative to generate pseudopregnant foster mothers.

Introduction

For many years, laboratory rodents, such as rats and mice, have been used to model human physiological and pathological conditions. Animal research has led to discoveries that were unattainable by any other means. Initially, genetic studies focused on the analysis of spontaneously occurring disorders and phenotypes that are considered to closely mimic the human condition¹. The development of genetic engineering methods allowed the introduction or deletion of specific genes to obtain a desired phenotype. Therefore, the generation of transgenic animals is recognized as a fundamental technique in modern research that allows studies of gene function in living organisms.

Transgenic animal technology has become possible through a combination of achievements in experimental embryology and molecular biology. In the 1960s, the Polish embryologist A. K. Tarkowski published the first work on mouse embryo manipulation during the early stages of development². Additionally, molecular biologists developed techniques to generate DNA vectors (i.e., carriers) for the inter alia introduction of foreign DNA into the animal’s genome. These vectors allow the propagation of selected genes and their appropriate modification, depending on the type of research that is conducted. The term “transgenic animal” was introduced by Gordon and Ruddle³.

The first widely accepted species that was used in neurobiology, physiology, pharmacology, toxicology, and many other fields of biological and medical sciences was the Norway rat, Rattus norvegicus⁴. However, because of the difficulty in manipulating rat embryos, the house mouse Mus musculus has become the dominant animal species in genetic research⁵. Another reason for the primacy of the mouse in such research was the availability of embryonic stem cell technology to generate knockout animals for this species. The most commonly used technique of transgenesis (2–10% of transgenic offspring relative to all born animals) is the microinjection of DNA fragments into a pronucleus of a fertilized oocyte. In 1990, this approach, which was first introduced in mice, was adapted for rats^6,7. Rat transgenesis by pronuclear injection is characterized by lower efficiency⁸ compared with mice, which is strictly related to the presence of elastic plasma and pronuclear membranes⁹. Although the survival of embryos after manipulation is 40–50% lower than in mice, this technique is considered a standard in the generation of genetically modified rats¹⁰. Alternative approaches that can guarantee efficient transgene incorporation and higher survival rates of injected zygotes have been investigated.

The key determinant of stable transgene expression and transmission to progeny is its integration into the host cell genome. Lentiviruses (LVs) have the distinctive feature of being able to infect both dividing and non-dividing cells. Their use as a tool for the incorporation of heterologous genes into embryos proved to be highly efficient¹¹, and transgenic individuals are characterized by stable expression of the incorporated DNA fragment. The efficacy of lentiviral vectors has been confirmed for the genetic modification of mice^12,13, rats^12,14, and other species¹¹. In this method, the LV suspension is injected under the zona pellucida of the embryo at the stage of two pronuclei. This technique essentially guarantees 100% survival of the embryos because the oolemma remains unaffected. The production of high-quality and relatively highly concentrated LV suspensions are crucial factors. However, lower concentrations of LV suspensions can be overcome by repeated injections¹¹, which increases the amount of viral particles at the egg surface while not affecting membrane integration. Embryos that are subjected to repeated injections into the perivitelline space develop further, and transgenic offspring can transmit the transgene through the germline. The efficiency of transgenic rat generation by lentiviral transgenesis can be as high as 80%¹².

Here, we describe the production of HIV-1-derived recombinant lentivirus that was pseudotyped with vesicular stomatitis virus (VSV) G envelope protein. The use of the second-generation packaging system VSV pseudotype determines the wide infectivity of viral particles and allows the production of highly stable vectors that can be concentrated by ultracentrifugation and cryopreserved. After titer verification, the vectors are ready to be used as a vehicle for transgene delivery into albino Wistar rat zygotes. After a series of injections, the embryos can be cultured overnight and transferred at the two-cell stage to foster mothers. At this point, one of two alternative approaches can be considered. The standard procedure utilizes pseudopregnant females as embryo recipients. However, when the pregnancy rate is low after mating with vasectomized males, the embryos can be implanted into pregnant Wistar/Sprague-Dawley (SD) females that are mated with fertile male rats with a dark fur color (e.g., Brown Norway [BN] rats). The color of the fur allows the distinction of offspring from natural pregnancy from offspring that originate from the transferred manipulated embryos.

Protocol

The production and application of viral vectors was in accordance with Biosafety Level 2 guidelines and was approved by the Polish Ministry of Environment. All experimental animal procedures that are described below were approved by the Local Ethical Committee. The animals were housed in individually ventilated cages at a stable temperature (21–23 °C) and humidity (50–60%) with ad libitum access to water and food under a 12 h/12 h light/dark cycle.

1. Lentiviral vector production

1. Transfection of HEK 293T cells
   NOTE: The protocol that is presented herein is designed for the transfection of twenty Ø10 cm culture dishes that produces approximately 200 mL of crude vector supernatant.
   1. Culture HEK 293T cells in DMEM medium that is supplemented with fetal bovine serum (10%, v/v) in a humidified CO₂ incubator at 37 °C. For transfection, prepare twenty 10 cm diameter plates, and seed 1.5–2 x 10⁶ HEK 293T cells per dish.
   2. When confluence reaches ~70%, transfect the cells using polyethylenimine (PEI) reagent, pH 7.0, at a ratio of 3 μg of PEI per 1 μg of DNA.
      1. Prepare the transfection mixture for five plates (prepare the number of repetitions according to the total number of dishes). To 1 mL of Dulbecco’s Modified Eagle Medium (DMEM; without serum), add the mixture of three plasmids so they reach a final amount of 25 µg of VSVg plasmid, 50 µg of delta R8.2, and 50 µg of coding plasmid.
      2. Pipette up and down, and add 125 µL of PEI at a concentration of 3 µg/µL. Incubate at room temperature for 15 min, inverting the tube three times during incubation. Add 200 µL of the transfection mixture per plate. Next, incubate the plates in a humidified CO₂ incubator at 37 °C.
2. Concentration of lentiviral vectors
   1. Forty-eight hours after transfection, harvest the medium that contains LV particles. Use 50 mL conical tubes.
      NOTE: When using a plasmid with a fluorescent tag, cells can be visualized at this point to verify transfection efficiency. A new portion of DMEM medium can be added, and cells may be incubated for an additional 24 h. The LV yield is comparable when collected at the 48 and 72 h time points after transfection.
   2. Centrifuge the medium at 3,000 x g for 5 min and room temperature to remove detached cells.
   3. Filter the supernatant (0.45 μm) and pour it into new tubes.
      NOTE: This step can be omitted.
   4. Add DNase I (RNase-free, 1 μg/mL) and MgCl₂ (1 mM), and incubate in a water bath at 37 °C for 15 min.
   5. Transfer the medium to disposable polyethylene tubes, and ultracentrifuge in a swinging rotor at 115,000 x g and 4 °C for 1.5 h.
   6. After centrifuging, gently drain the walls of the tubes from the medium residues.
   7. Soak the pellet with sterile phosphate-buffered saline (PBS; 70–80 µL per tube).
   8. Incubate for 2 h at 4–8 °C.
   9. Resuspend the viral vectors in PBS by gentle pipetting.
      CAUTION: Avoid foaming.
   10. Transfer to a 1.5 mL centrifuge tube and centrifuge at 7,000 x g and 4 °C for 30 s. Transfer the supernatant to a new tube. Repeat this step until no cellular debris pellet is visible.
   11. Aliquot and freeze at -80 °C. Avoid refreezing the LV aliquot.
3. Determination of virus titer using quantitative polymerase chain reaction
   NOTE: The titration of viral vectors is performed using quantitative PCR (qPCR). This method is based on amplifying a double-stranded 84 bp long DNA fragment within the long terminal repeat region of the viral genome¹⁵.
   1. Prepare the standard curve by making serial dilutions of the LV-coding plasmid: 1:500, 1:1,000, 1:5,000, 1:10,000, 1:100,000, and 1:1,000,000. Determine the number of copies of the plasmid that is used for the standard curve. Use the following formula: number of copies/µL = (concentration [g/µL] x 6.02 x 10²³ [number/mol]) / (660 [g/mol] x plasmid size [bp]), where 6.02 x 10²³ number/mol is Avogadro’s number, and 660 g/mol is the bp weight.
      NOTE: Online copy number calculators may be used.
   2. Prepare dilutions of the lentiviral suspension: 1:100, 1:500, and 1:1,000.
   3. Prepare the reaction mixture (volumes per well): 10 µL of qPCR Mastermix, 1 µL of 10 μM Forward primer, 1 µL of 10 μM reverse primer, and 7 µL of H₂O. Pipette the mixture into the wells of 96-well plates.
      NOTE: Forward primer: 5’-AGCTTGCCTTGAGTGCTTCA. Reverse primer: 5’-TGACTAAAAGGGTCTGAGGGA.
   4. Add 1 µL of each standard dilution and lentiviral suspension in triplicate.
   5. Run the qPCR according to the following parameters: 50 °C for 2 min, 96 °C for 5 min, and 35 cycles of 96 °C for 20 s, 60 °C for 40 s, and 70 °C for 1 min, followed by melt curve stage: 95 °C for 1 min and 60 °C at 30 s.
   6. Analyze the results by comparing the number of molecules that are received for each dilution to the standard curve. Determine the concentration of vector molecules as the average of three replicates for each dilution.
      NOTE: The presented quantification gives the physical concentration of the viral particles. It should not be treated as a functional titer.

2. Generation of transgenic rats

1. Superovulation and collection of fertilized embryos
   1. Administer gonadotropins.
      NOTE: To increase the number of collected embryos (approximately 30 per female), use immature 5-week-old Wistar females for hormonal stimulation.
      1. On Day 1 (12 PM–1 PM), intraperitoneally inject pregnant mare’s serum gonadotropin (PMSG; 25 IU per female). Prepare 1 mL aliquots of working solution at a concentration of 125 IU/mL by dissolving hormone powder in 0.9% NaCl. Store at -20 °C for up to 1 month or -80 °C for up to 6 months.
      2. On day 3 (12 PM–1 PM), intraperitoneally inject human chorionic gonadotrophin (hCG; 30 IU per female). Prepare 1 mL aliquots of working solution (150 IU/mL) by dissolving hormone powder in 0.9% NaCl. Store at -20 °C for up to 1 month or -80 °C for up to 6 months.
   2. After hCG administration, mate females 1:1 with sexually fertile males (3-10 months old).
   3. The next morning (day 4 at 8–10 AM), check the females for the presence of a vaginal plug. Check the vaginal opening for the presence of a whitish mating plug, which for best visualization should be checked early in the morning after the mating night. For embryo collection, use only females with a visible plug.
   4. Collect embryos at 10 AM. Sacrifice the animals to excise the oviducts, and collect the oviducts in a dish with pre-warmed M2 medium.
      1. Transfer the oviducts to a 35 mm dish that contains pre-warmed M2 medium with hyaluronidase from bovine testes at a concentration of 0.5 mg/mL.
      2. Open the walls of the oviduct using fine forceps under a stereomicroscope and press the ampulla (i.e., the swollen part of the oviduct that contains fertilized embryos that are surrounded by cumulus cells) until the embryos are freed.
         NOTE: Hyaluronidase enzymatically digests cumulus cells, releasing embryos.
         CAUTION: Prolonged exposure to hyaluronidase is deleterious to embryos; therefore, this step should last no longer than 5 min.
      3. To facilitate the release of embryos from cumulus cells, gently pipette them up and down using a glass transfer pipette that is connected to a mouth-operated aspirator tube.
         1. To produce the transfer pipette, pull a glass Pasteur pipette over a flame to produce a straight ~5-10 cm tip. Break the pipette leaving a ~4 cm tip.
      4. Wash the embryos a few times in M2 medium to remove hyaluronidase and cellular debris. Transfer the embryos to a 60 mm dish that contains (~50 µL) drops of pre-equilibrated M16 medium, covered by liquid paraffin or mineral oil, in a humidified 37 °C incubator with a 5% CO₂ atmosphere.
2. Microinjection of lentiviral vectors to one-cell-stage embryo under the zona pellucida
   NOTE: Use one-cell-stage embryos with two visible pronuclei for microinjection (Figure 1).
   1. Thaw the LV aliquot at room temperature and centrifuge at 10,000 x g and RT for 2 min to pellet any remaining cellular debris.
   2. Microinjection setup
      1. Prepare glass holding pipettes (borosilicate glass capillary) using a microforge. Pull the glass capillary over a flame to produce a 5–10 cm tip. Break the pipette leaving a ~4 cm tip. The outside diameter should be ~80–120 µm.
         NOTE: Ensure that the pipette tip is perfectly straight and smooth.
      2. Assemble the pulled pipette in a microforge with the tip in front of the heating filament. Heat the filament very close to the pipette tip and allow it to shrink to a diameter of ~15 µm (approximately 20% of embryo size). Position the pipette perpendicularly to the heating filament, 2–3 mm from the pipette tip, and begin to heat. The glass will soften. Heat until it reaches a 15° angle.
      3. Prepare microinjection borosilicate glass capillaries with a filament using a pipette puller. Insert the capillary in the pulling chamber. Run a ramp test (for the first time for new glass and every time after changing the filament). Set the Heat to the ramp value -10, Pull to 100, Velocity to 150 and Time to 100.
         NOTE: Modify the parameters to obtain an optimal injection capillary.
      4. Under a biosafety laminar flow hood, load approximately 2 µL of the viral solution into the microinjection pipette with a microloader tip.
      5. Prepare a microinjection dish (lid of 60 mm Petri dish) with a 100 µL drop of M2 medium (in the middle), covered by liquid paraffin or mineral oil.
      6. Mount the holding pipette and microinjection capillary that is loaded with viral solution to a micromanipulator and microinjection dish under an inverted microscope.
   3. Perform the microinjection.
      1. Transfer 15–20 one-cell-stage embryos to the M2 drop on the microinjection dish. Hold the embryo using a holding pipette.
      2. Using 400x magnification, inject the LV solution under the zona pellucida to the perivitelline space using the glass capillary that is connected to an automatic injector. Hold the capillary under the zona pellucida for a moment.
         NOTE: Using gentle positive pressure, the viral solution will flow continuously out of the injection capillary, but the volume of the suspension that is delivered cannot be controlled.
      3. Using a fine pipette, return the embryos to the culture dish in the incubator at 37 °C in a 5% CO₂ atmosphere. The number of injections of one zygote may vary and can be adapted based on the viral vector concentration.
         NOTE: The injected embryos can be transferred to foster mothers at the one-cell stage or incubated O/N in M16 medium before being transferred at the two-cell stage. Prolonged in vitro culture of rat embryos should be avoided.
3. Transfer of injected embryos to foster mothers
   1. Prepare foster mothers by mating sexually mature SD females with fertile BN males or with vasectomized SD males (the vasectomy procedure is described in section 3 below) on day 3 (for transferring embryos at the one-cell stage) or day 4 (for transferring embryos at the two-cell stage).
      NOTE: For oviduct transfer, use 0.5 days post coitum (dpc) females.
   2. The next morning, check SD females for a vaginal plug, and use only those with a visible plug.
   3. Perform embryo transfer.
      NOTE: Conduct the surgical procedure with sterile instruments under a stereomicroscope. Before the day of surgery, autoclave scissors, fine forceps, needle holder, and scalpel holder.
      1. Anesthetize a female with i.p. administration of ketamine (50 mg/kg) and medetomidine (0.5 mg/kg) solution.Test for reflexes to confirm anesthesia before starting the surgical procedure.
      2. Inject the animal subcutaneously with tolefenamic acid (2 mg/kg), butorphanol tartrate (1 mg/kg), and enrofloksacin (5–10 mg/kg) to prevent inflammation, pain, and infection, respectively.
      3. Apply ophthalmic ointment lubrication to both eyes to prevent corneal drying. Shave the fur from the back, and sterilize the skin with surgical scrub followed by 70% alcohol using sterile non-adhering pads. Allow the skin to dry.
      4. Inject the animal subcutaneously with 100 µL of 0.25% bupivacaine (local anesthetic) at the incision site. Transfer the animal in a prone position to a clean surface on a heating pad under the objective of a surgical microscope. Cover the rat with a sterile drape with a small hole cut over the lower back.
      5. Perform an approximately 2 cm skin incision, parallel to the lumbar vertebral column.
      6. Using sharp scissors, make a cut in the abdominal wall. Grab an ovarian fat pad using forceps, and pull out the ovary and oviduct and place them on gauze that is wetted with 0.9% NaCl.
      7. Aspirate M2 medium, three bubbles of air, and the embryos into the transfer capillary. Recommended total number of embryos to be transferred (unilateral or bilateral): pregnant female (≤ 15–16 embryos), pseudopregnant female (≤ 30 embryos).
      8. Make a small incision in the oviduct (between the infundibulum and ampulla) using micro-scissors, and insert the transfer pipette in the oviduct.
      9. Gently expel embryos and air bubbles from the pipette to the oviduct. With blunt forceps, place the reproductive tract back in the abdominal cavity.
      10. Suture the abdominal wall with polyglycolic acid absorbable sutures and close the skin incision with wound clips. Depending on the number of embryos that are available, repeat this procedure for the other oviduct.
      11. Inject the animal intraperitoneally with atipamezole (0.5 mg/kg) to reverse the effect of anesthesia.
      12. Transfer the animal to a clean cage and keep it on a warming plate to fully recover from anesthesia. Delivery in rats occurs after ~21 days.
          NOTE: When male BN rats are used for mating, only white pups are potentially transgenic; brown pups are from natural pregnancy.
      13. Collect tissue fragments (preferably from the ear) to genotype 3-week-old pups.

3. Vasectomy

NOTE: Before the day of surgery, autoclave scissors, fine forceps and needle holder.

1. Anesthetize a 5-week-old male SD rat with i.p. administration of ketamine (50 mg/kg) and medetomidine (0.5 mg/kg) solution. Test for reflexes to confirm anesthesia before starting the surgical procedure.
2. Administer tolfenamic acid (2 mg/kg), butorphanol tartrate (1 mg/kg), and enrofloksacin (5–10 mg/kg) subcutaneously to prevent inflammation, pain, and infection, respectively.
3. Apply ophthalmic ointment lubrication to both eyes to prevent corneal drying. Place the rat supine on a clean surface on a heating pad, and sterilize the skin on the testes with surgical scrub followed by 70% alcohol using sterile non-adhering pads. Allow the skin to dry. Cover the rat with a sterile drape with a small hole cut over the testes. Gently press the abdomen to expose the testes in the scrotal sac.
4. Using surgical scissors, make a ~0.5 cm incision in the middle of the scrotal sac. Locate the midline wall (whitish line) between the testes.
5. Make a 5 mm incision in the testis membrane close to the left side of the midline wall.
6. Carefully push the testis to the left and locate vas deferens (between the testis and midline) as a white duct with a single blood vessel.
7. Gently pull the vas deferens out of the scrotal sac using a watchmaker’s forceps. Hold the vas deferens with one pair of forceps, and cut it with fine scissors (or cauterize with red-hot tips of a second pair of forceps). Remove a ~1 cm fragment of the duct.
   NOTE: If cauterization is performed, hold the tip of the second pair of forceps in the flame.
8. Repeat the above procedure for the other testis. Suture the skin with polyglycolic acid absorbable sutures and inject the animal intraperitoneally with atipamezole (0.5 mg/kg).
9. Place the rat in a clean cage on a warming plate until the animal recovers from anesthesia.
   NOTE: Males can be used in the test matings after a ~2-week recovery period. After sterility is confirmed, they can be used for pseudopregnancy induction.

Results

Using the protocol described herein, lentiviral vectors that carried the Syn-TDP-43-eGFP construct were produced (physical LV titer = 3.4 x 10⁸/µL) and then could be used for one-cell-stage embryo subzonal injections. Only embryos with two visible pronuclei were subjected to the procedure. The number of injections of viral suspensions was determined experimentally. High implantation efficiency and a simultaneous lack of transgenic offspring were considered indicators of an insufficient number of viral particle...

Discussion

Advances in transgenic technologies have made rodent models an invaluable tool in biomedical research. They provide the opportunity to study genotype-phenotype relationships in vivo. Here, we present a widely available alternative for conventional transgenesis by pronuclear injections. The use of lentiviral gene transduction bypasses the need for demanding microinjections because viral vectors can be injected under the zona pellucida. This approach does not affect embryo integrity, which essentially guarantees a 100% sur...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
7500 Real Time PCR System	Applied Biosystems
Aerrane (isoflurane)	Baxter	FDG9623
Aspirator tube assemblies for calibrated microcapillary pipettes	Sigma	A5177-5EA
Atipam 5 mg/ml	Eurovet Animal Health BV	N/A	0.5 mg/kg
Baytril 25 mg/ml (enrofloksacin)	Bayer	N/A	5-10 mg/kg
Borosilicate glass capillaries with filament GC100TF-15	Harvard Apparatus Limited	30-0039	injection capillary
Bupivacaine 25 mg/ml	Advanz Pharma	N/A	0.25% in  0.9% NaCl
Butomidor 10 mg/ml (butorphanol  tartrate)	Orion Pharma	N/A	1 mg/kg
CELLSTAR Tissue Cell Culture Dish 35-mm	Greiner Bio-One	627160
CELLSTAR Tissue Cell Culture Dish 60-mm	Greiner Bio-One	628160
CellTram Oil	Eppendorf	5176 000.025
Cepetor (Medetomidine) 1 mg/ml	cp-pharma	N/A	0.5 mg/kg
Chorulon, Human Chorionic Gonadotrophin	Intervet	N/A	150 IU/ ml ml 0.9% NaCl
DMEM low glucose	Sigma Aldrich	D6048
DNase, RNase-free	A&A Biotechnology	1009-100
EmbryoMax Filtered Light Mineral Oil	Sigma	ES-005-C
Envelope protein coding plasmid for lentiviral vectors (VSVg plasmid)	ADDGENE	14888
FemtoJet	Eppendorf	4i /5252 000.013
Fetal Bovine Serum	Sigma Aldrich	F9665-500ML
Folligon, Pregnant Mare’s Serum Gonadotropin	Intervet	N/A	125 IU/ml in .9% NaCl
HEK 293T cells	ATCC	ATCC CRL-3216
Hyaluronidase from Bovine Testis	Sigma	H4272-30MG	0.5 mg/ml in M2 medium
Inverted Microscope	Zeiss	Axiovert 200
Ketamine 100mg/ml	Biowet Pulawy	N/A	50 mg/kg
Liquid Paraffin	Merck Millipore	8042-47-5
M16 medium EmbryoMax	Sigma	MR-016-D
M2 medium	Sigma	M7167
Magnesium Chloride 1M	Sigma Aldrich	63069-100ML
Microforge	Narishige	MF-900
Mineral Oil	Sigma	M8410-500ML
NaCl 0.9%	POLPHARMA OTC	N/A	sterile, 5ml ampules
Operation microscope	Inami Ophthalmic Instruments	Deca-21
Packaging system coding plasmid for lentiviral vectors  (delta R8.2 plasmid)	ADDGENE	12263
PEI reagent (Polyethylenimine, Mw ~ 25,000,),	Polysciences, Inc	23966-1
Penicilin-streptomycin	Sigma Aldrich	P0781-100ML
Phosphate Buffered Saline, pH 7.4, liquid, sterile-filtered, suitable for cell culture	Sigma Aldrich	806552-500ML
Puller	Sutter Instrument Co.	P-97
Reflex Clip Applier/Reflex Clips	World Precision Instruments	500345/500346
Safil, polyglycolic acid, braided, coated, absorbable threads	B.Braun Surgical	1048029
Stereomicroscope	Olympus	SZX16
Surgical Sewing Thread	B.Braun	C1048040
SYBR Green PCR Master Mix	Applied Biosystem	4334973
Tolfedine 4% (tolfenamic acid)	Vetoquinol	N/A	2 mg/kg
TransferMan NK2	Eppendorf	N/A
Trypsin EDTA solution	Sigma Aldrich	T3924-500ML
Ultracentrifuge	Beckman Coulter	Optima L-100 XP
VacuTip	Eppendorf	5175108.000	holders capillary
Vita-POS	Ursapharm	N/A	eye ointment
Warming Plate	Semic	N/A
Watchmaker Forceps	VWR	470018-868