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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
F4/80
- 亚型:
Rat IgG2a
- 形态:
PBS pH 7.2, 0.09% NaN3, 0.2% BSA
- 保存条件:
Store at 4°C and protected from prolonged exposure to light. Do not freeze.
- 克隆性:
Monoclonal Antibody
- 标记物:
FITC
- 适应物种:
Mouse
- 宿主:
Rat
- 应用范围:
FC
- 浓度:
Concentration:0.5 mg/ml
- 靶点:
Clone number:BM8
- 抗体英文名:
F4/80 Antibody-FITC;流式抗体
- 抗体名:
F4/80 Antibody-FITC;流式抗体
- 规格:
50/500 μg
克隆类型 :Rat Monoclonal Antibody;Clone number:BM8
货 号 :HT1610441
规 格 :50/500 μg ;
亚 型 :
Rat IgG2a
浓 度 :
Concentration:0.5 mg/ml
缓 冲 液 :
PBS pH 7.2, 0.09% NaN3, 0.2% BSA
产品描述 :
F4/80 is a 160 kD glycoprotein. It is characterized as a member of the epidermal growth factor (EGF)-transmembrane 7 (TM7) family. F4/80, also known as EMR1 or Ly71, has been widely used as a murine macrophage marker, which is expressed on majority of tissue macrophages including peritoneal macrophages, macrophages in lung, gut, thymus and red pulp of spleen (but not on the macrophages located in T cell areas of the spleen, lymph node and Peyer's patch), Kuffer cells, Langerhans cells, bone marrow stromal cells. F4/80 has also been shown on a subset of dendritic cells. The biological ligand of F4/80 has not been identified, but it has been reported that F4/80 is required for induction of CD8 T cells-mediated peripheral tolerance.
适用物种 :
Mouse
应用范围 :
FC
应用说明 :
The amount of the reagent is suggested to be used ≤ 0.5 µg /10^6 cells in 100 µl
保存条件 :
Store at 4°C and protected from prolonged exposure to light. Do not freeze.
标 记 物 :
FITC(其他荧光标记请咨询我们)
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文献和实验CNV Analysis Using TaqMan Copy Number Assays
Figure 2.13.4 Cts for un‐normalized and normalized DNA. The x axis represents the number of cycles and the y axis represents an arbitrary fluorescence unit. View Image
Application of Nexus Copy Number Software for CNV Detection and Analysis
An internet‐accessible computer with any modern Web browser [with any of the following systems: Windows (Win2k/WinXP/Vista/Windows7, 32/64 bit), Mac OS X, or Linux 32/64 bit] Nexus Copy Number
A Survey of Copy‐Number Variation Detection Tools Based on High‐Throughput Sequencing Data
., Meyerson, M., and Lander, E.S. 2009. High‐resolution mapping of copy‐number alterations with massively parallel sequencing. Nat. Methods 6:99‐103. Conrad, D.F., Pinto, D., Redon
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