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HT40232

Papanicolaou Stain, Modified EA 65

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About This Item

UNSPSC Code:
41116121
NACRES:
NA.47
MDL number:
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form

solution

Quality Level

shelf life

Expiry date on the label.

IVD

for in vitro diagnostic use

application(s)

hematology
histology

storage temp.

room temp

General description

For routine diagnostic cytology to aid in the identification and classification of exfoliative cells.

Application

Papanicolaou stain imparts a characteristic range of coloration to exfoliative cells of vaginal, cervical, prostatic and other body secretions, allowing critical examination of nuclei and cytoplasmic components.

Other Notes

Eosin Y (certified), 0.25% w/v,fast green FCF (certified), 0.004% w/v, and phosphotungstic acid, 0.4% w/v, in denatured alcohol with stabilizer

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Sens. 1 - STOT SE 2

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

55.4 °F - closed cup

flash_point_c

13 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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ข้อมูลสั้นๆเกี่ยวกับด้านเซลล์วิทยาบทบาทในการวินิจฉัยเซลล์และการใช้คราบมาตรฐานและพิเศษสำหรับการวิเคราะห์ด้วยกล้องจุลทรรศน์เพื่อตรวจจับความผิดปกติของเซลล์

Brief information on the field of cytology, its role in cytodiagnosis and the use of standard and special stains for microscopic analysis to detect cellular abnormalities.

Questions

  1. I want to perform conjunctival impression cytology, is Papanicolaou Stain Modified EA 65 appropriate if I want to fix and stain specimens with a combination of periodic acid-Schiff (PAS) and Gill’s modified Papanicolaou stains?

    1 answer
    1. This product has not been tested for its suitability in dual staining. When using the PAP Modified EA65 stain, the slides are also routinely stained with Gill's hematoxylin and OG-6. Using just the Papanicolaou Stain Modified EA 65 with a PAS stain would be considered "off-label" use by the FDA, as the PAP stain reagents are approved by the Food and Drug Administration for use in performing a standard PAP stain procedure.
      This application will need to be validated and properly documented for staining clinical specimens by the end-user.

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