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Merck
CN

86C

Sigma-Aldrich

白细胞碱性磷酸酶试剂盒

based on naphthol AS-BI and fast blue BB salt

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About This Item

UNSPSC代码:
12352106
eCl@ss:
42010105
NACRES:
NA.47

质量水平

保质期

Expiry date on the label.

IVD

for in vitro diagnostic use

应用

hematology
histology

运输

wet ice

储存温度

2-8°C

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应用

将外周血与骨髓样品混合起来制备显微镜玻片。制好的玻片随后在萘酚AS-BI碱性溶液及固蓝BB的混合液中孵育。所得的不可溶弥散性蓝色染料沉淀表明了碱性磷酸酶的活性位点。
白细胞碱性磷酸酶 (LAP) 试剂盒用于定性检测白细胞中的碱性磷酸酶活性。

仅试剂盒组分

产品编号
说明

  • Citrate Solution (915) 50 mL

  • FBB-Alkaline Solution (863) 10 mL

  • Naphthol AS-BI Alkaline Solution (861) 10 mL

  • Neutral Red Solution (N6264) 50 mL

  • Sodium Nitrite Solution (914) 10 mL

警示用语:

Danger

危险分类

Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1C - Skin Sens. 1 - STOT SE 3

靶器官

Respiratory system

补充剂危害

储存分类代码

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

法规信息

监管及禁止进口产品

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Ming-Tzu Tsai et al.
Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 27(9), 1169-1174 (2009-03-11)
Human mesenchymal stem cells (hMSCs) are a promising candidate cell type for regenerative medicine and tissue engineering applications by virtue of their capacity for self-renewal and multipotent differentiation. Our intent was to characterize the effect of pulsed electromagnetic fields (PEMFs)
Gregory M Cooper et al.
Tissue engineering. Part A, 16(5), 1749-1759 (2009-12-24)
The purpose of this study was to demonstrate spatial control of osteoblast differentiation in vitro and bone formation in vivo using inkjet bioprinting technology and to create three-dimensional persistent bio-ink patterns of bone morphogenetic protein-2 (BMP-2) and its modifiers immobilized
Julia Dotterweich et al.
PloS one, 11(5), e0155087-e0155087 (2016-05-10)
Multiple myeloma is one of the most common hematological diseases and is characterized by an aberrant proliferation of plasma cells within the bone marrow. As a result of crosstalk between cancer cells and the bone microenvironment, bone homeostasis is disrupted
Ankur Sharma et al.
Cytotechnology, 72(3), 489-497 (2020-03-04)
In the present study, we used a serum-free culture media to propagate goat putative spermatogonial stem cells (SSCs) and evaluated the effect of crucial growth factors on relative expression of some SSC markers and self-renewal related genes. The enriched SSCs
Ariana Darcy et al.
Bone, 50(6), 1294-1303 (2012-03-17)
Bone homeostasis can be compromised by an increase in osteoclast-mediated resorption and/or a decrease in osteoblast-mediated bone deposition. While many efforts have focused on treating osteoclast resorption, there has been less emphasis on identifying strategies for promoting osteoblast function. Herein

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