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艾美捷科技代理Boneslices品牌全系列产品


Boneslices是一家来自丹麦的公司,专注于生产牛皮质骨片。Boneslices公司提供用于200um, 400um厚度破骨细胞骨吸收功能检测Boneslice骨切片,适用于96孔板检测。


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▍Boneslices产品介绍

在开始陷窝实验前,需用培养基对骨切片进行复水处理。由外周血单核细胞(PBMC)或共培养体系生成的成熟/未成熟破骨细胞,均可接种于骨切片表面。根据破骨细胞的成熟状态及存在因子的差异,吸收陷窝将在3-14天内形成。通过抗酒石酸酸性磷酸酶(TRAcP)活性检测可观察破骨细胞数量,而甲苯胺蓝染色则可显现吸收陷窝与吸收沟的形成(见图2)。

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▍产品参数

产品描述:本品为用于破骨细胞骨吸收实验的皮质骨切片。

规格参数:直径:6mm(适配96孔板)

厚度:0.2mm(最适用免疫荧光、共聚焦显微镜及延时记录);0.4mm(最适用下游分析)

运输条件:骨切片在室温环境下运输。

用途说明:牛皮质骨切片专为96孔板中的破骨细胞陷窝/骨吸收实验设计。


产品名称型号规格
Bone Slices0.4 mm50 pcs;100 pcs;300 pcs;500 pcs
Bone Slices0.2 mm50 pcs;100 pcs;300 pcs;500 pcs



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2.5比1.pngexocell.jpg

艾美捷科技代理VisualProtein品牌。

VisualProtein成立于2005年,致力于通过提供创新的科研产品与服务推动生物领域发展。凭借在蛋白质组学、免疫学及细胞学领域的专业深耕,不断拓宽科学研究的可能性边界。


Visual Protein的产品包括:

分类品名货号
ProteomicsWestern Blot Tool BoxBOX12
ProteomicsWestern Blot Tool Box with LuminolPen(LH03-10)BOX12-03
ProteomicsBlockPRO™ Blocking BufferBP01-1L
ProteomicsBlockPRO™ Protein-Free Blocking BufferBF01
ProteomicsBlockPRO™ 1 Min Protein-Free Blocking BufferBM01
ProteomicsLuminolPen™, HRP systemLH03
ProteomicsLumiFlash™ Prime Chemiluminescent Substrate, HRP SystemLF01-500
ProteomicsLumiFlash™ Ultima Chemiluminescent Substrate, HRP SystemLF08-500
ProteomicsLumiFlash™ Infinity Chemiluminescent Substrate, HRP SystemLF16-500
ProteomicsLumiFlash™ Femto Chemiluminescent substrate, HRP SystemLF24-100
ProteomicsExtractPRO™ Protein Extraction ReagentEP05-30
ProteomicsRIPA Cell Lysis BufferRP05
ProteomicsDual-Range™ BCA Protein Assay KitBC03-500
ProteomicsDual-Range™ Bradford Reagent (1X)BR01-500
ProteomicsDual-Range™ Bradford Reagent (5X)BR05-500
ProteomicsDual-Range™ Bradford Protein Assay Kit (5X)BR05-500-K
ProteomicsVisPRO™ Blue-One Protein StainVB01-500
ProteomicsVisPRO™ 5 Minute Protein Stain KitVP01
Proteomics6X Laemmli SDS Sample Buffer, non-reducing(without beta-mercaptoethanol)SBN06-15
Proteomics6X Laemmli SDS Sample Buffer, reducing(with beta-mercaptoethanol)SBR06-15
Immunoassay bufferImmunoEX immunoassayDevelopment Kit(TBST)IEX001
Immunoassay bufferImmunoEX ImmunoassayDevelopment Kit (TBS)IEX002
Immunoassay bufferImmunoEX TBST BufferIE01-500
Immunoassay bufferImmunoEX TBS BufferIE02-500
Immunoassay buffermmunoEX Protein-BasedImmunoassay Buffer(TBSTIE03-500
Immunoassay bufferImmunoEX Protein-Based lmmunoassay Buffer (TBS)IE04-500
Immunoassay bufferImmunoEX Protein-Free Immunoassay Buffer(TBSTIE05-500
Immunoassay bufferImmunoEX Protein-Free Immunoassay Buffer (TBS)IE06-500
SupplementCytoMore Cell RescueSupplementCTO1-1BT
SupplementHybriMore™ Hybridoma Culture Supplement*HB01-1L
BufferPBS Buffer, 10XPBS10-1L
BufferPBS Tween-20 Buffer, 10XPBST10-1L
BufferTBS Buffer, 10XTBS10-1L
BufferTBS Tween-20 Buffer, 10XTBST10-1L
BufferTBS Tween-20 Buffer, 25XTBST200P
BufferSDS-PAGE Running Buffer, 10XRB10-1L
BufferSDS-PAGE Running Buffer, powder packRB500P
BufferWestern Blot Transfer Buffer, 10XWTB10-1L
BufferWestern Blot Transfer Buffer, powder packWTB500P



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Dendritics.jpg

Dendritics公司主要关注人类树突状细胞,希望找到能够促使CD34+造血前体细胞转化为树突状细胞(在GM-CSF和TNF-alpha存在的情况下)的细胞因子。在1992-2005年间,大量的研究使得研究者对人类树突状细胞的产生、细胞通路、C-type凝集素受体的功能及Toll-like受体的活性有了更深的理解。

 

DENDRITICS was started in 2005 by former members of SCHERING PLOUGH Laboratory for Immunological Research (LIR) in Dardilly, France. From their long experience at LIR, the team members of DENDRITICS have gathered complementary scientific and technological knowledge in different areas of immunology. The initial focus of LIR was in the biology of B lymphocytes, elaboration of human monoclonal antibodies, and in cytokine discovery (IL-3, IL-4, IL-7, IL-10, IL-17, GM-CSF) together with our colleagues of DNAX Research Institute in Palo Alto, California.

 

Our interest in cytokines led to the finding that human dendritic cells (DCs) could be generated in vitro from CD34+ hematopoietic progenitors cultured in the presence of GM-CSF and TNF-alpha.

 

The period from 1992 to 2005 saw the specialization of LIR in DC biology and was fuelled by a large-scale effort to discover and study the function of genes specifically expressed by these cells. This program led to a number of findings that contributed in particular to understanding the heterogeneity of DCs, the pathways regulating DC migration, the function of C-type lectin receptors in DCs and the activity of Toll-like receptors in DCs. Many novel genes were discovered through screening of cDNA libraries or through monoclonal antibodies raised against DCs.

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