86R
Leukocyte Alkaline Phosphatase Kit
based on naphthol AS-BI and fast red violet LB
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UNSPSC Code:
12352106
NACRES:
NA.47
eCl@ss:
42010105
Servicio técnico
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Permítanos ayudarleQuality Level
shelf life
Expiry date on the label.
IVD
for in vitro diagnostic use
dilution
(for histology)
application(s)
hematology
histology
shipped in
wet ice
storage temp.
2-8°C
Application
Leukocyte Alkaline Phosphatase (LAP) kits are intended for the qualitative demonstration of alkaline phosphatase activity in white blood cells.
Peripheral blood or bone marrow preparations are fixed to a microscope slide. The film is then incubated in a mixture of naphthol AS-BI alkaline solution with fast red violet LB. The resulting insoluble diffuse, red dye deposit indicates sites of alkaline phosphatase activity.
Solo componentes del kit
Referencia del producto
Descripción
- Citrate Solution (915) 50 mL
- FRV-Alkaline Solution (862) 10 mL
- Hematoxylin Solution, Gill No. 3 (kit only) 50 mL
- Naphthol AS-BI Alkaline Solution (861) 10 mL
- Sodium Nitrite Solution (914) 10 mL
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Irrit. 2 - STOT RE 2 Oral
target_organs
Kidney
flash_point_f
Not applicable
flash_point_c
Not applicable
wgk
WGK 2
Clase de almacenamiento
10 - Combustible liquids
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Clive H Glover et al.
PLoS computational biology, 2(11), e158-e158 (2006-11-24)
Stem cell differentiation involves critical changes in gene expression. Identification of these should provide endpoints useful for optimizing stem cell propagation as well as potential clues about mechanisms governing stem cell maintenance. Here we describe the results of a new
Terence P Gade et al.
PloS one, 6(7), e22608-e22608 (2011-07-30)
The purpose of this study was to develop a paradigm for quantitative molecular imaging of bone cell activity. We hypothesized the feasibility of non-invasive imaging of the osteoblast enzyme alkaline phosphatase (ALP) using a small imaging molecule in combination with
Raha Favaedi et al.
The International journal of developmental biology, 60(4-6), 103-110 (2016-07-09)
Histone H3 lysine 9 methylation has been shown to be a critical barrier to efficient cell reprogramming. This discovery allows the assessment of the cell pluripotency state by considering the extent of H3K9 methylation vs. acetylation at the same position.