- 入驻时间: 2015-11-06
- 联系人:顾磊
- 电话:021-60514606
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- Email:shybio@126.com
收到小鼠神经束膜细胞时如无异常情况,请在显微镜下观察细胞密度,如为贴壁细胞,未超过80%汇合度时,将培养瓶中培养液吸出,留下10ml培养液继续培养;超过80%汇合度时,请按细胞培养条件传代培养。如为悬浮细胞,吸出培养液、1000转/分钟离心2分钟,吸出上清,管底细胞用新鲜培养基悬浮细胞后移回培养瓶。
小鼠神经束膜细胞Perineurial fibroblasts are of mesenchymal origin and form the perineurium. The perineurium plays an important role in maintaining the integrity of the internal peripheral nerve environment by creating a physical barrier that, under physiologic condition, limits the entry of biologically active proteins, infectious agents, and blood-borne cells into the nerve bundles [1]. The perineurial fibroblasts are characterized by distinct ultrastructural features, including non-branching thin cytoplasmic processes coated by an external lamina and joined at their ends by a tight junction, few organelles, actin and vimentin filaments, and numerous pinocytotic vesicles [2]. Perineurial fibroblasts are initially recruited from the surrounding mesenchyme to form a loose, permeable sheath around axons and Schwann cells, where they are separated by the extracellular matrix. These cells later undergo a mesenchymal-to-epithelial transition to form tight junctions and organize into the perineurium. Perineurial fibroblasts are immunoreactive for vimentin and epithelial membrane antigen but not for the Schwann cell marker S-100 [3].
MPNF from ScienCell Research Laboratories are isolated from postnatal day 8 mouse sciatic nerve. MPNF are cryopreserved at passage one and delivered frozen. Each vial contains >5 x 10^5 cells in 1 ml volume. MPNF are characterized by immunofluorescence with antibodies specific to vimentin, S-100, GFAP and CD90. MPNF are negative for mycoplasma, bacteria, yeast, and fungi. MPNF are guaranteed to further expand for 5 population doublings under the conditions provided by ScienCell Research Laboratories.
Recommended Medium
It is recommended to use Fibroblast Medium (FM, Cat. #2301) for culturing MPNF in vitro.
小鼠神经束膜细胞传代方法:
收到细胞后,取出培养瓶在倒置显微镜下观察细胞生长情况。
(一)如果细胞未长满,用75%酒精喷洒整个瓶**后放到超菌台内,严格无菌操作,打开细胞培养瓶,吸出培养液,仅留下10ml培养液在瓶内继续培养。
(二)如果细胞已长满,即可进行传代培养。具体步骤如下:
1. 弃去培养液,用PBS(不含钙,镁离子)洗1-2次。
2. 加1ml消化液(0.25%Trypsin-0.53mM EDTA)于培养瓶中,小鼠神经束膜细胞倒转放于37度培养箱1-3分钟预热,然后又将培养瓶倒转大约30秒后,在倒置显微镜下观察细胞消化情况,若细胞大部分变圆分散,轻敲几下培养培养瓶,细胞随即脱落下来。
3. 加入6-8ml完全培养基,吸出,分到新的培养瓶中。1:3~1:6传代;2~3天1次。
。
注意:传代后一半用我们的培养基,一半用你们的,以免细胞不适应而造
成生长不好。
冻存方法: 冻存液:基础培养基+5%DMSO+20%FBS
储存:液氮储存
小鼠神经束膜细胞其它细胞系展示表:
yb-hxbz-096 人肝癌细胞 QGY-7703 规格25毫升/株.
yb-hxbz-097 人肝癌细胞 Bel-7402 规格25毫升/株.
yb-hxbz-098 人肝癌细胞 Bel-7404 规格25毫升/株.
yb-hxbz-099 人肝癌细胞 Bel-7405 规格25毫升/株.
yb-hxbz-100 人肝癌细胞 Hep3B2.1-7 规格25毫升/株.
yb-hxbz-101 人肝癌细胞 SK-HEP-1 规格25毫升/株.
yb-hxbz-102 人肝癌亚力山大细胞 HCCC-9810 规格25毫升/株.
yb-hxbz-103 人胆囊癌细胞 GBC-SD 规格25毫升/株.
yb-hxbz-104 正常人肝细胞 L-02 规格25毫升/株.
yb-hxbz-105 人胚肝细胞正常 QSG-7701 规格25毫升/株.
yb-hxbz-106 人肝细胞正常 HL-7702 规格25毫升/株.
yb-hxbz-107 CCL13张氏肝细胞正常 Chang liver 规格25毫升/株.
yb-hxbz-108 人肝星形细胞正常 LX-2 规格25毫升/株.
yb-hxbz-109 人肝内胆管上皮细胞 HIBEpiC 规格25毫升/株.
yb-hxbz-110 人高转移肝癌细胞 LM3 规格25毫升/株.
yb-hxbz-111 人肝癌细胞系 LM-6 规格25毫升/株.
yb-hxbz-112 人低转移肝癌细胞 MHCC97-L 规格25毫升/株.
yb-hxbz-113 人肝癌细胞 HepG2/2-15 规格25毫升/株.
yb-hxbz-114 人肝癌细胞 9204 规格25毫升/株.
yb-hxbz-115 人肝癌细胞 HuH-7 规格25毫升/株.
yb-hxbz-116 人肝癌细胞 FL62891 规格25毫升/株.
yb-hxbz-117 人胆管细胞型肝癌细胞 HCCC-9810 规格25毫升/株.
yb-hxbz-118 人肝癌细胞 HCC-9724 规格25毫升/株.
yb-hxbz-119 人肝癌细胞 HHCC 规格25毫升/株.
yb-hxbz-120 人肝癌细胞系 Hep-3B 规格25毫升/株.