129S6

Origin:

Taconic received 129S6 inbred model stock from GenPharm International from two sublines originating from Dr. Martin Evan's colony in 1992. The mice were derived by embryo transfer in 1993. The resulting offspring were heterozygous at Gpi1 for the 'a' and 'c' alleles. Homozygous Gpi-1c brother x sister mice were selected in the Foundation Colony at F8 and became the common ancestors for all subsequent Taconic breeders. The Taconic foundation colony was at F42 in 2005.

Availability:

Genetics:

• Strain Profile: Acy1^s, Akp1^b, Amy1^a, Apoa1^b, Car2^a, Es1^b, Es3^c, Esd^b, Es11^a, Ggc^a, Glo1^a, Got2^b, Gpi1^c, Gpt1^a, Gr1^a, Gus-s^b, H6pd^b, Hbb^d, Idh1^a, Ldr1^a, Mod1^a, Mpi1^b, Neu1^b, Pep3^b, Pgm1^b, Pgm2^a, Pnp^a, Trf^b, Sod1^a
• Immunology: H2^b
• Other: Ptprc^b

Coat Color Loci:

Color:

Species:

Initial Publication:

Simpson, EM, et. al; (1997) "Genetic Variation Among 129 substrains and its Importance for 'Targeted Mutagenesis' in Mice." Nature Genetics; Vol. 16(1), p. 19

Animal Diet:

n = 250 per sex at MPF and RF health standards from all global colonies.
High and Low represent mean +/- 2 standard deviations.
Based on sample size the charts above represent ~90% of the population.
All growth curves represent animals housed in our barriers, at our standard density and fed NIH31-M diet. Variations at customer facilities will alter expected growth curves.
Growth charts are provided only as a guide, if a specific weight criteria is needed please order animals by weight.

Average litter size: 8

Phenotyping Procedures:

A quantity of twenty mice (ten males and ten females) was submitted for testing, strain identified as Line 129SVE (129S6/SvEvTac), age 7 weeks. Mice were received at RBU 3, Taconic Biotechnology, Albany NY and acclimated for three days on irradiated NIH #31M rodent diet and sterilized water ad lib, sterile contact bedding (paper chip) and a 12:12 light:dark cycle. All animals appeared normal during this period and routine health surveillance of this colony detected no microbial pathogens. Mice were assigned study unique identification numbers (males 1-10, females 11-20).

All mice were fasted in metabolic cages and an overnight urine sample was collected. Urine analysis was performed using Multistix 10 SG (Bayer). Strips were read and recorded as per the manufacturer's instructions, and the results are presented in Table 1.

A terminal blood sample was taken from Carbon Dioxide - anesthetized mice via cardiac puncture. The collected blood was divided into two samples. One sample was treated with EDTA and stored at 4°C for hematological evaluation. Another sample was allowed to clot at 4°C for 30 minutes, and then centrifuged at 7000rpm for 10 minutes, and the serum was decanted and frozen at -80°C for clinical chemistry analysis. A slide smear was made from a single drop of whole blood. Frozen serum, chilled whole blood, and slides were delivered to LabCorp (RTP, NC) for analysis; the results are presented in Table 2. Unless otherwise indicated, serum chemistry data is generated from a Hitachi 717 automated analyzer and hematological data is generated from a Celldyne 3500. WBC differential counts are performed manually. No blood samples were obtained from mouse #16.

All mice were euthanized and bodyweights were recorded. Representative tissues were collected, weighed, and immersion fixed in 10% Neutral Buffered Formalin. Tissues were delivered to the Taconic lab for histological preparation and evaluation. Tabulation of organ weights is presented in Table 3. The pathologist's summary and detailed histological descriptions follow.

Model 129SVE (strain: 129S6/SvEvTac) Reproductive Data: