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Process of isolating
chromosomes of White mice

By: Heydee A. Santos
Chromosome Preparation:
 Chromosome of the bone marrow cells and
testis were prepared afte one hour, the
treatment into 0.025% colchicine (Fig. 6) at

0.25%ml per kilogram body weight. (Fig.10)
the mice were sacrificed by cervical
dislocation. The femur yields the bone
marrow cells which were pumped out into the
isotonic solution (2.2% sodium Citrate)
through the sucking and pumping motion of
the syringe with a fine needle.
Each Mouse was Weighed Prior to
Colchicine Treated
The Mice were Pre-Treated with
0.25ml Colchicine one hour
before
Chromosome Preparation:
The testis was pulled just above the penile organ
through an incision, again these was placed in an
isotonic solution 2.2% (Sodium Citrate) for
teasing to a fine suspension though a syringe. The
bone marrow cells and testis suspension were
transferred to a dryer tube. Spinning for five (5)
minutes (Fig. 8), the supernatant was removed for
cell breaking and stocking in a hypotonic solution
(1.0% sodium citrate) for twelve (12) minutes.
Fixation follows, for the testis cells suspension,
three (3) fixation processed are needed. Flicking
of the tube is also needed for the recovering of
metaphase. Four (4) fixations are needed for the
bone marrow cells suspension.
Slide Plating:
 Dried clean microscope slides (25x 75 mm)
previously soaked in a 1:1 ratio of Ethanol – Acetic
acid solution, using a fine – tipped pasteur pipettes,
a suspension was topped on a pre cleaned slide and
dried by blowing the suspension under an infra – red
light. (Fig. 9). Slide was stained with temporary
stain Toluidine – o, and covered with cover slips, and
observed with Zeiss standard 18 microscope camera
attachment using 25 – 40x objectives and a 10x / 18
oculars with plerapo 100 / 1.3 oil immersion
objective, green filter and colpan 21 high copy film,
it is an important Panchromatic fild packed by
Comlumbia
Suspension was Topped o a PreCleaned Slide under an Infra – red
Light.
Analysing chromosome
Normal chromosome of testis
Chromosomal Aberration on
testis
Chromosomal Break at Control – Irridiated
Mouse Bone Marrow Cells at Mitotic Metaphase
Sticky Chromosome
Reason of using white mice as a
biological indicator

The mice were used as they are good
biological indicator organism for the
following reason:
(1) readily available (2) low cost (3) ease
of handling (4) good chromosome
condition and (5) have good
correlation with other test organism.
Thank You!

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Isolating Chromosomes

  • 1. Process of isolating chromosomes of White mice By: Heydee A. Santos
  • 2. Chromosome Preparation:  Chromosome of the bone marrow cells and testis were prepared afte one hour, the treatment into 0.025% colchicine (Fig. 6) at 0.25%ml per kilogram body weight. (Fig.10) the mice were sacrificed by cervical dislocation. The femur yields the bone marrow cells which were pumped out into the isotonic solution (2.2% sodium Citrate) through the sucking and pumping motion of the syringe with a fine needle.
  • 3. Each Mouse was Weighed Prior to Colchicine Treated
  • 4. The Mice were Pre-Treated with 0.25ml Colchicine one hour before
  • 5. Chromosome Preparation: The testis was pulled just above the penile organ through an incision, again these was placed in an isotonic solution 2.2% (Sodium Citrate) for teasing to a fine suspension though a syringe. The bone marrow cells and testis suspension were transferred to a dryer tube. Spinning for five (5) minutes (Fig. 8), the supernatant was removed for cell breaking and stocking in a hypotonic solution (1.0% sodium citrate) for twelve (12) minutes. Fixation follows, for the testis cells suspension, three (3) fixation processed are needed. Flicking of the tube is also needed for the recovering of metaphase. Four (4) fixations are needed for the bone marrow cells suspension.
  • 6. Slide Plating:  Dried clean microscope slides (25x 75 mm) previously soaked in a 1:1 ratio of Ethanol – Acetic acid solution, using a fine – tipped pasteur pipettes, a suspension was topped on a pre cleaned slide and dried by blowing the suspension under an infra – red light. (Fig. 9). Slide was stained with temporary stain Toluidine – o, and covered with cover slips, and observed with Zeiss standard 18 microscope camera attachment using 25 – 40x objectives and a 10x / 18 oculars with plerapo 100 / 1.3 oil immersion objective, green filter and colpan 21 high copy film, it is an important Panchromatic fild packed by Comlumbia
  • 7. Suspension was Topped o a PreCleaned Slide under an Infra – red Light.
  • 11. Chromosomal Break at Control – Irridiated Mouse Bone Marrow Cells at Mitotic Metaphase
  • 13. Reason of using white mice as a biological indicator The mice were used as they are good biological indicator organism for the following reason: (1) readily available (2) low cost (3) ease of handling (4) good chromosome condition and (5) have good correlation with other test organism.