搜索结果: 'easysep direct'

Falcon® 圆底管，带细胞滤网扣盖，5 mL 无菌聚苯乙烯圆底管，配有尼龙网细胞过滤器卡扣盖
RoboSep™-16垃圾袋 RoboSep™-16垃圾袋
RoboSep™-S附加服务包 RoboSep™- S -全自动细胞分选仪器
RoboSep™分选管套装 RoboSep™分选管套装（9个塑料管+尖端保护器）
技术公告
Simplify Your PBMC Isolations with the EasySep™ Direct Human PBMC Isolation Kit

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细胞类型：

B 细胞，NK 细胞，T 细胞，单个核细胞，单核细胞，淋巴细胞

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科学海报
Rapid, Automated Lymphocyte Isolation Directly from Whole Blood with EasySep™ Direct

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Conference：

EFI 2019

产品号#：

21000

20155

20119

19655

19655RF

89671

89671RF

89684

89684RF

19671

19671RF

19684

19684RF

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RoboSep™- S

RoboSep™分选试管套装（9个塑料管+吸头保护器）

RoboSep™ 吸头组件抛光剂

EasySep™ Direct人总淋巴细胞分选试剂盒

RoboSep™ Direct人总淋巴细胞分选试剂盒

EasySep™ Direct HLA交叉配型T细胞分选试剂盒

RoboSep™ Direct HLA交叉配型T细胞分选试剂盒

EasySep™ Direct HLA交叉配型B细胞分选试剂盒

RoboSep™ Direct HLA交叉配型B细胞分选试剂盒
1:44

视频
Cell Isolation Directly from Whole Blood without RBC Lysis or Centrifugation: EasySep™ Direct

发布日期: 10/10/2014
6:13

视频
How to Isolate Cells Directly from Whole Blood - EasySep™ Direct Protocol, EasyEights Magnet

发布日期: 03/09/2015
产品手册
EasySep™ Direct 仅需20分钟，从全血中分选细胞

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品牌：

EasySep

产品号#：

19264

19655

19661

19662

19663

19664

19666

19669

19674

19665

19657

19659

19655RF

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EasySep™ Direct 人Naïve B细胞分选试剂盒

EasySep™ Direct人总淋巴细胞分选试剂盒

EasySep™ Direct人T细胞分选试剂盒

EasySep™ Direct人CD4+ T细胞分选试剂盒

EasySep™ Direct人CD8+ T细胞分选试剂盒

EasySep™ Direct 人B-CLL细胞分选试剂盒

EasySep™ Direct人中性粒细胞分选试剂盒

EasySep™ Direct人单核细胞分选试剂盒

EasySep™ Direct人B细胞分选试剂盒

EasySep™ Direct人NK细胞分选试剂盒

EasySep™ Direct 人CTC富集试剂盒

EasySep™ Direct人Pan-粒细胞分选试剂盒

RoboSep™ Direct人总淋巴细胞分选试剂盒
技术窍门
Isolate Virtually Any Cell Type Using EasySep™ or EasySep™ Release Indirect Selection Kits
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EasySep™ 红细胞去除试剂

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品牌：

EasySep

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Spring H et al. (DEC 2005) Proceedings of the National Academy of Sciences of the United States of America 102 50 18111--6

Chemokines direct endothelial progenitors into tumor neovessels.

Tumor neovasculature substantially derives from sprouting of existing vessels,whereas the functional contribution of bone marrow-derived progenitors to neovessels remains controversial. We used transgenic mouse models of multistep carcinogenesis to monitor incorporation of bone marrow-derived cells into the neovasculature and to elucidate mechanisms of endothelial precursor cell (EPC) recruitment into the tumor microenvironment. We unequivocally demonstrate integration of bone marrow cells into the tumor vasculature as a late event in carcinogenesis that temporally correlates with VEGF release by the tumor and mobilization of circulating EPC in the periphery. Moreover,we demonstrate a chemokine-dependent mechanism of EPC homing into tumor,whereby neovessels of late-stage tumors release a battery of CC chemokines,which direct CCR2(+) and CCR5(+) progenitors into the vasculature. Thus,we show that tumor vessels promote their own growth and development in a self-amplifying fashion. View Publication

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产品号#：

05900

05950

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