Stains Flashcards

1
Q

When preparing smear preps which blood specimens are collected?

A

EDTA + Capillary

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2
Q

What is the purpose of Eosin Y?

A

cytoplasm pink

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3
Q

What is the purpose of methylene blue?

A

nucleus + DNA = blue

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4
Q

How is smears fixed?

A

methanol

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5
Q

What will an acidic stain dye?

A

basic tissue

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6
Q

What will an alkaline stain dye?

A

Acidic tissue

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7
Q

What is a polychromatic dye?

A

compound of dyes which exhibit multiple colours.

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8
Q

What is polychroming?

A

forms other dyes spontaneously or by oxidation

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9
Q

What are Romanowsky stains sensitive to?

A

pH

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10
Q

What are the basic components of a RWSKY stain?

A
  • Methylene Blue
  • Azure
  • Eosin compounds
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11
Q

What are examples of RWSKY stains?

A
  • Giemsa
  • Wrights
  • Jenner
  • Lillie-Wrights
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12
Q

What is metachromasia?

A

tissue stains diff colour than the dye.

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13
Q

What are examples of cellular components which stain purple rather than blue?

A
  • Mast cell granules
  • Cartilage
  • Mucin
  • Amyloid
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14
Q

What does methylene blue require to oxidize?

A

Silver oxide

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15
Q

What is the principle of silver oxide?

A
  • oxidize methylene blue into methylene violet (Azure A) methylene blue (Azure B)
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16
Q

What is critical about the buffer conditions?

A

pH

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17
Q

What happens if the buffer is greater than 7.0?

A

Alkaline = Blue

18
Q

What happens if the buffer is less than 7.0?

A

Acidic = pink

19
Q

What are the purposes of buffer?

A
  • dilute the stain (1:1)
  • Rinse slides
20
Q

What might a diluted buffer cause?

A

weak stain

21
Q

What might an alkaline stain cause?

A

mask abnormalities

22
Q

What might a acidic stain cause?

A

unacceptable slide because granules other than Eosinophils stain red.

23
Q

What are corrective actions for an alkaline stain?

A

1- check pH
2- Shorten stain time
3- prolong buffer

24
Q

What are corrective actions for an acidic stain?

A

1- lengthen stain time
2- check buffer + stain pH
3- Shorten buffer

25
Q

What might inadequate fixation cause?

A
  • washing off slide
  • poor nuclear details
  • poor staining of granules
  • fix water contaminations
  • drying artifacts
26
Q

What is the staining process?

A

1- Fixation
2- Staining
3- Wash
4- Dry

27
Q

What is stain precipitate?

A

black / dark granules

28
Q

How do you remove stain precipitates?

A
  • additional staining for 5-10 seconds
  • dip in 30% methanol
29
Q

What does LAP stand for?

A

Leukocyte Alkaline Phosphatase

30
Q

What does LAP do?

A
  • Non cancerous cells will have dark blue granules
  • Myelogenous leukemia = few granules
31
Q

What category of stains for LAP fall under?

A

cytochemical stains

32
Q

Which part of the LAP stain is responsible for causing the granular reaction?

A

alkaline phosphatase

33
Q

What is the LAP reading?

A

enzymatic activity is proportional to staining degree

34
Q

What inhibits LAP?

A

EDTA

35
Q

What are examples for decreased LAP?

A

-CML
-Sickle cell anemia

36
Q

What are examples for increased LAP?

A

-3rd T pregnancy
-Leukemoid reaction

37
Q

What are the leukocytes which LAP read?

A
  • Band / segmented
    neutrophils, myelocytes, metamyelocytes
38
Q

What is the normal LAP range?

A

30 -100

39
Q

How is the range established?

A

Every lab will determine its own range

40
Q

How do you determine the LAP score?

A

count 100 NEUT give each a score