ES7152

ENG Scientific Pneumocystis Carinii Stain Kit

Manufacturer: Fischer Scientific

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Pack Size SKU Availability Price
Pack of 2 ES7152-Pack-of-2 In Stock ₹ 16,684.20

ES7152 - Pack of 2

₹ 16,684.20

In Stock

Quantity

1

Base Price: ₹ 16,684.20

GST (18%): ₹ 3,003.156

Total Price: ₹ 19,687.356

Type

Ethanol 95%

Quantity

2 x 250 mL

Includes

Toluidine Blue O Stain

For Use With (Application)

In vitro diagnostic use

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Description

  • Pneumocystis carinii is an opportunist which causes a diffuse interstitial pneumonia in patients with impaired immune systems
  • The disease itself can be classified as epidemic or sporadic; the latter occurring in patients who have an underlying immunosuppression
  • In this procedure, a sulfation reagent of glacial acetic acid and sulfuric acid (not included) is used for the removal of background material
  • This allows the Pneumocystis carinii cysts to be visualized more easily after staining with Toluidine Blue 0
  • Diagnosis of Pneumocystis carinii pneumonia can frequently be made on bronchoalveolar lavage (BAL) or on touch preparations of pulmonary tissue (open lung biopsies and transbronchial biopsies)
  • Recommended Procedures: BAL Specimens: Using a 50 mL tube, centrifuge for 15 minutes at 2000 x g
  • Aspirate all but the bottom 5 mL of supernatant
  • With a Pasteur pipette, aspirate the sediment plus approximately 1 mL of the remaining 5 mL of fluid
  • Transfer material to a 15 mL centrifuge tube, gently mix and prepare smear by spreading a drop over a 1 cmm area
  • If concentrated specimen is very thick or mucoid, spread over entire slide with care being taken not to make the smear too thick
  • Dry the slides on a heating block at 50 - 55°C
  • Allow to cool before staining
  • Touch Preparations: When dry, process in same manner as slides of BAL
  • Preparation of Sulfation Reagent: In a dry coplin jar submerged in a plastic tub filled with cool water (not below 10°C), mix 45 mL of glacial acetic acid with 15 mL of concentrated sulfuric acid and stir gently with glass rod
  • Carefully place smears in reagent for 10 minutes
  • Mix immediately and again after 5 minutes
  • Gently rinse with water for 10 minutes
  • Drain excess water and stain with Sol
  • I for 3 - 5 minutes
  • Rinse with Sol
  • II followed by Sol
  • III for 10 seconds each
  • Clear in Sol
  • IV, two changes each for 10 seconds and mount
  • Results: The cyst forms appear as lavender structures (cup-shaped) approximately 5 urn in diameter
  • The cyst outline is distinct, and the internal region stains uniformly
  • Note: A negative bronchoalveolar lavage does not rule out an infection with Pneumocystis carinii
  • Other diagnostic procedures may be necessary.

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