LONDON REGIONAL TRANSGENIC AND GENE TARGETING FACILITY



Similar documents
A POWERFUL IN VITRO FERTILIZATION

Assisted Reproductive Technologies at IGO

FACTORS THAT AFFECT IN VITRO FERTILIZATION USING CRYOPRESERVED MOUSE SPERM

Revised minimum standards for in vitro fertilization, gamete intrafallopian transfer, and related procedures

Proceedings, Applied Reproductive Strategies in Beef Cattle September 11 and 12, 2007, Billings, Montana NEW TECHNOLOGIES FOR REPRODUCTION IN CATTLE

REPRODUCTIVE MEDICINE AND INFERTILITY ASSOCIATES Woodbury Medical Arts Building 2101 Woodwinds Drive Woodbury, MN (651)

Consent to Perform Preimplantation Genetic Screening (PGS) using. Comparative Genomic Hybridization (acgh) or Next Generation Sequencing (NGS)

Reproductive technologies. Lecture 15 Introduction to Breeding and Genetics GENE 251/351 School of Environment and Rural Science (Genetics)

INFORMED CONSENT AND AUTHORIZATION FOR IN VITRO FERTILIZATION OF PREVIOUSLY CRYOPRESERVED OOCYTES

ANS 3319C Reproductive Physiology and Endocrinology Artificial Insemination in Cattle. Objectives. What are the advantages and disadvantages of AI?

ART IVF - NO.1 IVF - IVF

Genetic Technology. Name: Class: Date: Multiple Choice Identify the choice that best completes the statement or answers the question.

MASSACHUSETTS GENERAL HOSPITAL VINCENT REPRODUCTIVE MEDICINE AND IVF

Authorized By: Holly C. Bakke, Commissioner, Department of Banking and Insurance.

Guide to IVF Laboratory Results

Headquarters in Sioux Center, IA 1

Human Umbilical Cord Blood CD34 + Progenitor Cell Care Manual

How to construct transgenic mice

In - Vitro Fertilization Handbook

Von Mäusen und Menschen E - 1

Breeding Strategies for Maintaining Colonies of Laboratory Mice

How To Get A Refund On An Ivf Cycle

DNA Fingerprinting. Unless they are identical twins, individuals have unique DNA

How to construct transgenic mice

European IVF Monitoring (EIM) Year: 2008

Unit B: Understanding Animal Reproduction. Lesson 3: Understanding Animal Reproduction Technology

Assisted reproductive technologies (ART) in Canada: 2011 results from the Canadian ART Register

Preimplantation genetic diagnosis new method of screening of 24 chromosomes with the Array CGH method...2

Fertility care for women diagnosed with cancer

NON MEDICARE FEES CANBERRA FERTILITY CENTRE VERSION JANUARY 2015 AM QWB 295

European IVF Monitoring (EIM) Year: 2010

Understanding Animal Reproduction Technology

Artificial Insemination in Cattle

Breeding Strategies for Maintaining Colonies of Laboratory Mice

The Jackson Laboratory. Mouse Colony Management and Breeding Strategies

Infertility Services Medical Policy For University of Vermont Medical Center and Central Vermont Medical Center employer groups

AGE & FERTILITY: Effective Evaluation & Treatment I. LANE WONG, MD, FACOG.

Basic Concepts Recombinant DNA Use with Chapter 13, Section 13.2

Areas of Concern. Reproductive Ethics: Issues &

50% Off Cycle 3 $ 9,900 $ 8,700 $ 7,500

Frozen-EZ Yeast Transformation II Catalog No. T2001

Appendix J. Genetic Implications of Recent Biotechnologies. Appendix Contents. Introduction

Stem Cell Quick Guide: Stem Cell Basics

Best Practices for Efficient Mouse Colony Management

IVF OVERVIEW. Tracy Telles, M.D.

Thermo Scientific Nunc Products for InVitro Fertilization. security, safety and reproducibility. for your valuable. samples

DARTMOUTH-HITCHCOCK MEDICAL CENTER Lebanon, New Hampshire IN VITRO FERTILIZATION PROCEDURE DESCRIPTION

Clinical Policy Committee

it right? activity (page 4) to highlight ethical issues associated with IVF

Consent for Frozen Donor Oocyte In Vitro Fertilization and Embryo Transfer (Recipient)

Human Adult Mesothelial Cell Manual

How to construct transgenic mice

Training Programme in. Assisted Reproductive Technologies:

Nordic Fertility Society. Quality Guide. Checklist for ART Clinic and ART laboratory

Fertility Facts and Figures 2008

Recommended Resources: The following resources may be useful in teaching this

Reproductive Technology. Chapter 21

Symposium on RECENT ADVANCES IN ASSISTED REPRODUCTIVE TECHNOLOGY

CONSENT TO PARTICIPATE IN THE IN VITRO FERTILIZATION-EMBRYO TRANSFER PROGRAM

Illinois Insurance Facts Illinois Department of Financial and Professional Regulation Division of Insurance

Genetics for the Novice

Why. IVF Centers Prof. Zech. fertility treatment? for your. choose the

The impact of genomic selection on North American dairy cattle breeding organizations

Assisted reproductive technology in Australia and New Zealand 2010

Ethical issues in assisted reproductive technologies. Effy Vayena

Preimplantation Genetic Diagnosis. Evaluation for single gene disorders

30% Off Cycle 1. Possible Preliminary Discussions With Contract Negotiations

A rapid and effective nonsurgical artificial insemination protocol using the NSET TM device for sperm transfer in mice without anesthesia

Design of conditional gene targeting vectors - a recombineering approach

CONCEPT DOES NOT REQUIRE AN UP FRONT DEPOSIT (Except for Standard IVF/ICSI/FET where out of pocket costs must be paid in advance)

Lesbian Pregnancy: Donor Insemination

ANS 3319C Reproductive Physiology and Endocrinology Techniques for In-Vitro Embryo Production

Bacterial Transformation Post lab Questions:

Frozen Donor Embryo Transfer Price List, EDI 2016

Clinical Reference Group Quality & Safety Committee Governing Body. Policy Screened

Biotechnology and Recombinant DNA (Chapter 9) Lecture Materials for Amy Warenda Czura, Ph.D. Suffolk County Community College

Artificial Reproductive Technologies I: insemination

Guidance For Research Involving Human Embryonic Stem Cells, Germ Cells, And Cells Obtained From Cord Blood

Egg and sperm donation in the UK:

Answer Key Problem Set 5

Human Peripheral Blood Mononuclear Cell (PBMC) Manual

Differentiation = Making specialized cells. Your body needs stem cells. What is a stem cell?

Heredity - Patterns of Inheritance

Course: AG 534 Zoology - Science of Animal Reproduction

European Medicines Agency

ASSISTED REPRODUCTIVE TECHNOLOGIES (ART)

Preimplantation Genetic Diagnosis (PGD) for Fanconi Anemia and HLA matching

Biology Notes for exam 5 - Population genetics Ch 13, 14, 15

Human CD4+T Cell Care Manual

Choosing the sex of babies: Ethical debate

Consultations & other investigations

ANS Reproductive Physiology of Domestic Animals (Spring 2015)

FINANCIAL INFORMATION FOR PATIENTS

Day -1 RETRIEVAL OF OVARIES AND OOCYTE COLLECTION AND MATURATION

Transcription:

LONDON REGIONAL TRANSGENIC AND GENE TARGETING FACILITY SPERM CRYOPRESERVATION AND IN VITRO FERTILIZATION RESOURCE PACKAGE For information, contact: Dr. Christopher Pin, PhD, Scientific Director London Regional Transgenic and Gene Targeting Facility Phone: 519-685-8600 ext. 53073 E-mail: cpin@uwo.ca Ms. Linsay Drysdale, B.Sc., ES Cell Technician London Regional Transgenic and Gene Targeting Facility Phone: 519-685-8600 ext. 53624 E-mail: Linsay.Drysdale@lhsc.on.ca I. OUTLINE OF SERVICES The London Regional Transgenic and Gene Targeting (LRTGT) Facility provides services for investigators to preserve and bank genetically modified mouse lines through sperm cryopreservation and then rederive these and other lines via in vitro fertilization. Sperm cryopreservation is a simple, efficient and inexpensive method for archiving large numbers of genetically-engineered mice. It involves the isolation of mature sperm from the caudae epididymides of two fertile males followed by rapid freezing and storage of the sperm in liquid nitrogen. In vitro fertilization can reconstitute a mouse line from fresh or frozen sperm. It can also be used for embryo cryopreservation, to rapidly expand a mouse line from a sperm harvested from a single male, rescue lines where males are poor breeders and to rederive a mouse line into a Specific Pathogen Free (SPF) barrier facility. The standard process of in vitro fertilization involves mixing an aliquot of fresh or frozen sperm with oocytes isolated from superovulated females of the appropriate background. After 4 to 6 hours the oocytes are washed and incubated overnight. Following overnight incubation, all resulting 2-cell embryos are transferred to pseudopregnant females.

II. SERVICE DESCRIPTION Sperm Cryopreservation We will cryopreserve the sperm of two males from a given mouse line. For best results, we recommend that the client supply two breeding males between 3 and 6 months of age that have been mated 5 to 7 days prior to the cryopreservation session. Sperm cryopreservation yields 10 straws of frozen sperm per male. An extra straw from each cryopreservation will be frozen and used to perform an IVF to demonstrate the ability of the thawed sperm to produce fertilized embryos. Our sperm cryopreservation service includes: Harvesting and freezing sperm from two males per strain Quality control test consisting of thawing one straw and performing an IVF to demonstrate the viability of the cryopreserved sperm Long-term storage in liquid nitrogen Provide a written report detailing the specifics of the session Current modifications to the sperm cryopreservation method have greatly improved the quality of thawed sperm, particularly for C57BL/6 strains. However, even with these improvements, the fertilization capacity of thawed sperm can differ significantly among mouse lines and the fertility of the individual males used as sperm donors. In Vitro Fertilization We provide in vitro fertilization with fresh or frozen sperm based on the needs of the investigator. For best results, we recommend that the client supply two breeding males between 3 and 6 months of age that have been mated 5 to 7 days prior to the IVF session. If frozen sperm is used in the procedure we can use an aliquot of sperm cryopreserved by the LRTGT and stored on site or sperm that has been cryopreserved by an external institution and shipped directly to us. Our in vitro fertilization service includes: Collection of sperm from donor male mice or thawing of cryopreserved sperm Incubation of sperm with oocytes collected from superovulated females Transfer of resulting 2-cell embryos to pseudopregnant females

III. PRIOR TO SUBMITTING A SPERM CRYOPRESERVATION OR IVF REQUEST 1. Consult the Director or LRTGT Technician The LRTGT will work with the investigator to determine the timing of the request and provide feedback on the best options for preserving the line. In some cases, sperm cryopreservation may not be the best option. 2. Have a valid animal protocol that includes the cryopreservation or IVF protocol. We are working to establishing a blanket protocol within the LRTGT that covers cryopreservation and IVF, but do not currently have this available. The LRTGT technician can provide details to include in your protocol. 3. Ensure sufficient numbers of proven breeder males. The LRTGT recommends that two proven breeders between 3 and 6 months of age are supplied by the client. IV. SUBMITTING A SPERM CRYOPRESERVATION REQUEST 1. Complete sperm cryopreservation request form (see below). Submit a request form (see included form) to the LRTGT Director or technician, including an animal protocol number covering handling of the mice. We will work with you to establish a time frame that fits both the LRTGT and the investigator. 2. Set aside two proven males for the cryopreservation session. The client should set aside two breeding males between the ages of 3 and 6 months. Males should be mated a week prior to the cryopreservation and then rested for 5 to 7 days. V. ONCE WE HAVE A SPERM CRYOPRESERVATION REQUEST: The LRTGT staff will: 1. Collect fresh sperm from the caudal epididymides of the two male mice provided by the client. 2. Freeze 10 straws of sperm per male and store in liquid nitrogen. 3. Perform an in vitro fertilization using one straw of frozen sperm to determine its capacity to produce fertilized embryos. 4. Provide a written report detailing the specifics of the session. We will inform the client of the quality of the sperm at the time of collection and the results of the test thaw and IVF. The LRTGT maintains an electronic database of all genetically modified mouse lines frozen down. This database can include an in depth description of the frozen line with relevant publications, MTA forms, etc. Please inform the LRTGT Director if you do not wish to have this information available to other London-based researchers. NOTE: The fertilization capacity of thawed sperm can differ significantly among mouse lines

and the fertility of the individual males used as sperm donors. V. SUBMITTING AN IN VITRO FERTILIZATION REQUEST 1. Complete an in vitro fertilization request form (see below). Submit a request form (see included form) to the LRTGT Director or Technician, including an animal protocol number covering handling of the mice. We will work with you to establish a time frame that fits both the LRTGT and the investigator. 2. Set aside two proven males for the IVF session. The client should set aside two breeding males between the ages of 3 and 6 months. Males should be mated a week prior to the IVF and then rested for 5 to 7 days. The females used in the procedure will be provided or ordered by the LRTGT. -OR- 3. Provide the LRTGT with two aliquots of cryopreserved sperm. The LRTGT will thaw two straws of sperm that have been frozen by us and stored in our facility. Alternatively, two aliquots of sperm frozen by an external source may be used. These samples must be shipped directly to the LRTGT. All females used in the procedure will be ordered by the LRTGT. VI. ONCE WE HAVE THE IVF REQUEST: The LRTGT staff will: 1. Collect fresh sperm from the caudal epididymides of the male mice provided by the client. An aliquot of this sperm will be incubated for 4-6 hours with oocytes collected from superovulated females. If frozen sperm is used, the sperm will be thawed and allowed to capacitate prior to incubation with the oocytes. After incubation with the sperm, the oocytes will be washed and incubated overnight. 2. All resulting two-cell embryos will be transferred to pseudopregnant females. 3. Provide a written report detailing the specifics of the session. We will inform the client of the quality of the sperm collected or thawed, the number of fertilized embryos transferred, and the number of pups born. NOTE: In vitro fertilization results will vary with genetic background and the quality of the males used. We do not guarantee that any given IVF procedure will produce a large number of pups. If you need to change or cancel your session, you must inform the LRTGT at least 3 days in advance to avoid the minimum charge. VI. COSTS: Sperm cryopreservation $500 In vitro fertilization session $1000

IVF session cancellation without notification $50 Cost of hormones Cost of females Health Testing $500 (If required) Note: Additional costs may be incurred depending upon the strain of females used as oocyte donors.

VII. INFORMATION SPECIFIC FOR CRYOPRESERVATION/IVF: MOUSE LINE TO BE CRYOPRESERVED: UWO ANIMAL PROTOCOL NUMBER: HAS THIS LINE BEEN SUCCESSFULLY CRYOPRESERVED AND RECOVERED PREVIOUSLY: YES NO Male Female Strain / Background Genotype Homozygous/ Heterozygous Date of Birth or Age of Mice Total Number Available KNOWN PHENOTYPE OF THIS LINE: PRESENT LOCATION OF ANIMALS: PERFORM A TEST FREEZE AND THAW: YES NO IF NO TO TEST FREEZE AND THAW, A SIGNATURE IS REQUIRED I agree that The London Regional Transgenic and Gene Targeting Facility will use all reasonable efforts and will not be held responsible for poor results obtained without the prior knowledge of a test freeze and thaw. QUALITY CONTROL TEST PER SESSION (if able): YES NO INVESTIGATOR TO PERFORM THE FOLLOWING: Hormone Injections: YES NO TRAINING REQUIRED Check Plugs: YES NO TRAINING REQUIRED Oviduct Collection: YES NO TRAINING REQUIRED REPRODUCTIVE PERFORMANCE OF MOUSE LINE: Females responsive to superovulation: YES NO UNKNOWN Average litter size: Males reproductively challenged? If so please explain:

LONDON REGIONAL TRANSGENIC AND GENE TARGETING SERVICE REQUEST FORM: DATE: CONTACT INFORMATION: INVESTIGATOR NAME: DEPT. ROOM NO. BLDG. MAILING ADDRESS TEL FAX E-MAIL ADDRESS LAB CONTACT (IF DIFFERENT FROM PI) E-MAIL ADDRESS UWO ANIMAL PROTOCOL NUMBER (INTERNAL REQUESTS) SERVICE REQUESTED (please check all that apply): Pronuclear Injection Cryopreservation (are embryos heterozygous or homozygous?) Rederivation Sperm cryopreservation In vitro fertilization PROJECT DETAILS: TITLE: For Pronuclear Injection Requests, Transgene Vector Name: DNA Information: (concentration/volume/buffer/size (kb)): Short Description of Expectations (including potential developmental problems):

PLEASE ATTACH: 1) Gel photo of DNA sample for electroporation or pronuclear injection 2) Detailed plasmid map (including diagnostic restriction enzyme cut sites and fragment lengths) 3) Visual evidence that genotyping can be performed by PCR (Pronuclear Injection Request) 4) Information specific for cryopreservation of mouse embryos or sperm BILLING INFORMATION: Please complete the following information for billing purposes: NAME OF FINANCIAL OFFICER FINANCIAL OFFICER S TELEPHONE NUMBER CHARGE TO ACCOUNT NUMBER (INTERNAL REQUESTS) CHARGE TO PO NUMBER (EXTERNAL REQUESTS) PUROLATOR ACCOUNT NUMBER (FOR SHIPPING PURPOSES) PREFERRED MOUSE COURIER ACCOUNT NUMBER SIGNATURE OF ACCOUNT HOLDER This signature indicates your acceptance of all outlined charges in the LRTGT information packages. SUBMIT THIS FORM TO: DR. CHRISTOPHER PIN LONDON REGIONAL TRANSGENIC AND GENE TARGETING FACILITY VICTORIA RESEARCH LABS, ROOM A5-134 790 COMMISSIONERS ROAD E. LONDON, ON N6A 4L6 PHONE: (519) 685-8600 X53073 FAX: (519) 685-8186 EMAIL: cpin@uwo.ca Date Received: By: