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ROCEDURES


BACTI-STAIN

Auramine O Staining
Auramine-Rhodamine Staining

Gram Staining
Kinyoun Acid Fast Staining
Phenolic Acridine Orange Staining
Ziehl-Neelson Acid Fast Staining

CONCENTRATION SYSTEMS

SED-CONNECT™ (Illustrated)
SED-CONNECT™
PARA-SED™(Illustrated)
PARA-SED™
MICRO-SED™


PARASITOLOGY

Modified Acid Fast Staining
Para-Fix™: PVA
Para-Fix™: SAF
Trichrome Blue Staining

Wheatley's (modification of Gomori)
Trichrome
Wrights Dip Stat Staining
Wrights One Step Staining


OTHER PROCEDURES
(in PDF FORMAT)

Auramine O
Buffy Coat Protocol
Combination Modified Acid Fast, Modified Trichrome
Combination Thick-Thin Blood Film
Determination of Parasitemia
Fecal Concentration, Micro-Sed
Fecal Concentration, Para-Sed
Fecal Concentration, Sed-Connect
Giemsa Blood Stain
Gram Stain Table
Gram Stain
Modified Kinyoun (Cold)
Modified Trichrome Stain
(Ryan Blue)

Wheatley's Trichrome Stain
Wright's Dip STAT Kit
Wright's Dip STAT Stain
Wright's ONE-STEP Stain


 

 

 

 

PARA-SED™ (ILLUSTRATED)
       
  1. Add 8-10 drops of surfactant to specimen vial, cap securely and shake or vortex.   2. Insert Par-SedÈ filtration into specimen vial. Invert complete device and tap on counter top to facilitate filtering.   3. Unscrew Para-SedÈ device from 50 ml centrifuge tube.  
             
       
  4. Add saline or 10% formalin to red fill line on the 50 ml centrifuge tube, then add ~5 ml of ethyl acetate. Attach screw cap to the tube and vigorously shake.   5. Centrifuge for 10 minutes at 500 xg.   6. Invert tube to pour off supernatent and debris layer. Ring inside of tube with cotton applicator stick.  
             
           
  7. Re-suspend pellet with a few drops of saline or formalin and examine under a microscope.          
             
 
   
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