推荐产品
一般描述
PP。最大上样体积300 µl。基本适配所有主要的微孔板离心机。每个孔口周围的凸起环可最大限度减少可能的交叉污染。孔板可用热封膜密封，如耐DMSO密封膜（横切），带字母数字编码。
特点和优势
- BRAND® 96 孔微孔板，U 形底是一种深孔板，非常适合凝集和其他需要搅拌和洗涤样品的测定。
- 具有圆形井底，没有边缘。
- 孔口周围的凸起环可防止可能的交叉污染。
- 与一系列微孔板离心机兼容。
- 可使用合适的密封垫或自粘密封膜牢固密封。
- 用于准确识别的字母数字代码。
- 由高透明度的医用级聚丙烯（PP） 制成，有助于提高样品的可见性。
- 耐大多数溶剂，包括 DMSO、苯酚和氯仿。
法律信息
BRAND is a registered trademark of BRAND GMBH + CO KG
Gefei Chen et al.
Communications biology, 3(1), 32-32 (2020-01-22)
Molecular chaperones play important roles in preventing protein misfolding and its potentially harmful consequences. Deterioration of molecular chaperone systems upon ageing are thought to underlie age-related neurodegenerative diseases, and augmenting their activities could have therapeutic potential. The dementia relevant domain
Stephen D Carter et al.
Science advances, 6(14), eaay9572-eaay9572 (2020-04-10)
The endoplasmic reticulum (ER) is a highly dynamic network of membranes. Here, we combine live-cell microscopy with in situ cryo-electron tomography to directly visualize ER dynamics in several secretory cell types including pancreatic β-cells and neurons under near-native conditions. Using
SeongJun Han et al.
Oncoimmunology, 9(1), 1737368-1737368 (2020-04-22)
Regulatory T cells are integral to the regulation of autoimmune and anti-tumor immune responses. However, several studies have suggested that changes in T cell signaling networks can result in T cells that are resistant to the suppressive effects of regulatory
Rosalie Heilig et al.
Life science alliance, 3(6) (2020-04-30)
Caspase-1 drives a lytic inflammatory cell death named pyroptosis by cleaving the pore-forming cell death executor gasdermin-D (GSDMD). Gsdmd deficiency, however, only delays cell lysis, indicating that caspase-1 controls alternative cell death pathways. Here, we show that in the absence
Atsuya Nishiyama et al.
Nature communications, 11(1), 1222-1222 (2020-03-08)
Stable inheritance of DNA methylation is critical for maintaining differentiated phenotypes in multicellular organisms. We have recently identified dual mono-ubiquitylation of histone H3 (H3Ub2) by UHRF1 as an essential mechanism to recruit DNMT1 to chromatin. Here, we show that PCNA-associated
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