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BAH136800040

Flowmi® 细胞过滤器

porosity 40 μm, for 1000 uL Pipette Tips, pack of 50 ea

同義詞:

compact laboratory sample filters, facs sample filtration, small sample filter, small sample pipette tip filter

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About This Item

分類程式碼代碼:
41104932
NACRES:
NB.01

材料

white

無菌

sterile

包裝

pack of 50 ea
pkg of (supplied in a tray)

製造商/商標名

Bel-Art H13680-0040

孔徑

40 μm porosity

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相關類別

一般說明

Scienceware® Flowmi 细胞过滤器可在流动或分析前快速有效地过滤小体积样品(最多 1000μl)。专利申请中。

特點和優勢

  • 过滤小样本量时保留部分体积
  • 降低 FLOW 或 FACS 堵塞的可能性
  • 用作有效过滤细胞碎片的工具
  • 与您常用的移液器枪头配套使用;Flowmi 适合大多数 1000μl 枪头,包括 Fisherbrand Sure-One、VWR brand、Axygen、Nichiryo 和 Eppendorf 等
  • 紧凑型托盘可容纳 50 个 Flowmi 细胞过滤器,随时可用于压片,并可将附件安装在您的吸头上;具有滑动盖,易于单手使用
  • 当用于层流净化罩时,包装在可重新密封袋中以保持无菌性

其他說明

推荐用于具有以下特征的样本: 最大浓度为 2MM 细胞/ml。

法律資訊

Flowmi is a registered trademark of SP Scienceware, Division of SP
Scienceware is a registered trademark of SP Scienceware, a division of SP

分析證明 (COA)

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Zong Miao et al.
PLoS genetics, 16(9), e1009018-e1009018 (2020-09-15)
Reverse causality has made it difficult to establish the causal directions between obesity and prediabetes and obesity and insulin resistance. To disentangle whether obesity causally drives prediabetes and insulin resistance already in non-diabetic individuals, we utilized the UK Biobank and
Marcus Alvarez et al.
Scientific reports, 10(1), 11019-11019 (2020-07-06)
Single-nucleus RNA sequencing (snRNA-seq) measures gene expression in individual nuclei instead of cells, allowing for unbiased cell type characterization in solid tissues. We observe that snRNA-seq is commonly subject to contamination by high amounts of ambient RNA, which can lead
Pavlo A Nesterenko et al.
Proceedings of the National Academy of Sciences of the United States of America, 118(3) (2021-01-13)
T cell receptors (TCRs) are generated by somatic recombination of V/D/J segments to produce up to 1015 unique sequences. Highly sensitive and specific techniques are required to isolate and identify the rare TCR sequences that respond to antigens of interest.
Jeremy Lotto et al.
Cell, 183(3), 702-716 (2020-10-31)
The cellular complexity and scale of the early liver have constrained analyses examining its emergence during organogenesis. To circumvent these issues, we analyzed 45,334 single-cell transcriptomes from embryonic day (E)7.5, when endoderm progenitors are specified, to E10.5 liver, when liver

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