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80316 80311 µ-Slide 三合一通道培养载玻片-80316


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可调节趋化梯度,并把三个分开的液体融汇到一个通道得三合一μ培养载玻片
动态的流动梯度,较大的时间分辨率
可变化的梯度区域用于趋化细胞的捕获

详细信息 在线询价

货号

产品名称规格(个/盒)
80316µ-Slide  三合一通道培养载玻片,ibiTreat底部处理15
80311µ-Slide  三合一通道培养载玻片,无包被15

 

接口

Female Luer

通道内高度

1/3 mm

每溶液柱容积

60 µl

总生长面积

1.23 cm²

通道数量

3 in 1

最小刻度

1 mm

总通道容积

60 µl

底部:ibidi标准底

所有通道高度

0.4 mm

 

 

 

应用:

高达三个不同液体的流体分析

激光捕获进行细胞分选

内径流体集中化


技术特点:

3通道合一

生成微流体双向梯度

和ibidi泵系统和其他泵完全兼容

永远是平流层流动

误差仅为毫米级

流体试剂盒中也提供

设置可变化的化学趋化剂浓度梯度:

图3.jpg

 不同位置有不同的浓度梯度分布。流体环境由ibidi流体剪切力系统提供。

 

图4.jpg

Overlapping gradients for chemotactical cell trapping. Switching

times of some seconds allow fast gradient switching, so that

cytoskeletal dynamics can be observed using fluorescence microscopy.

 

 实验案例:

图5.jpg

 


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动态的流动梯度,较大的时间分辨率
可变化的梯度区域用于趋化细胞的捕获","Detail":"

货号<\/p><\/td>

产品名称<\/td>规格(个/盒)<\/td><\/tr>
80316<\/span><\/td>µ-Slide  三合一通道培养载玻片,ibiTreat底部处理<\/td>15<\/td><\/tr>
80311<\/span><\/td>µ-Slide  三合一通道培养载玻片,无包被<\/td>15<\/td><\/tr><\/tbody><\/table>

 <\/p>

接口<\/strong><\/p><\/td>

Female Luer<\/p><\/td>

通道内高度<\/strong><\/p><\/td>

1/3 mm<\/p><\/td><\/tr>

每溶液柱容积<\/strong><\/p><\/td>

60 µl<\/p><\/td>

总生长面积<\/strong><\/p><\/td>

1.23 cm²<\/p><\/td><\/tr>

通道数量<\/strong><\/p><\/td>

3 in 1<\/p><\/td>

最小刻度<\/strong><\/p><\/td>

1 mm<\/p><\/td><\/tr>

总通道容积<\/strong><\/p><\/td>

60 µl<\/p><\/td>

底部:ibidi标准底<\/p><\/td><\/tr>

所有通道高度<\/strong><\/p><\/td>

0.4 mm<\/p><\/td>

 <\/p><\/td>

 <\/p><\/td><\/tr><\/tbody><\/table>

 <\/p>

应用:<\/strong><\/span><\/p>

高达三个不同液体的流体分析<\/span><\/p>

激光捕获进行细胞分选<\/span><\/p>

内径流体集中化<\/span><\/p>


技术特点:<\/strong><\/span><\/p>

3通道合一<\/span><\/p>

生成微流体双向梯度<\/span><\/p>

和ibidi泵系统和其他泵完全兼容<\/span><\/p>

永远是平流层流动<\/span><\/p>

误差仅为毫米级<\/span><\/p>

流体试剂盒中也提供<\/span><\/p>

设置可变化的化学趋化剂浓度梯度:<\/span><\/p>

\"图3.jpg\"<\/span><\/p>

 不同位置有不同的浓度梯度分布。流体环境由ibidi流体剪切力系统提供。<\/span><\/p>

 <\/p>

\"图4.jpg\"<\/span><\/p>

Overlapping gradients for chemotactical cell trapping. Switching<\/em><\/span><\/p>

times of some seconds allow fast gradient switching, so that<\/em><\/span><\/p>

cytoskeletal dynamics can be observed using fluorescence microscopy.<\/em><\/span><\/p>

 <\/p>

 实验案例:<\/span><\/p>

\"图5.jpg\"<\/span><\/p>

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