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C8-D30 [Astrocyte type III clone]细胞

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  • 产品名称:C8-D30 [Astrocyte type III clone]细胞
  • 产品型号:C8-D30 [Astrocyte type III clone]
  • 产品展商:HZbscience
  • 产品文档:无相关文档
  • 发布时间:2018-06-18
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简单介绍
C8-D30 [Astrocyte type III clone]细胞应如何避免细胞污染,细胞污染的种类可分成**、酵母菌、霉菌、病毒和霉浆菌。主要的污染原因为无菌操作技术不当、操作室环境不佳、污染之血清和污染之细胞等。严格之无菌操作技术、清洁的环境、与品质良好之细胞来源和培养基配制是减低污染之*好方法。C8-D30 [Astrocyte type III clone]细胞何时须更换培养基?视细胞生长密度而定,或遵照细胞株基本数据上之更换时间,按时更换培养基即可。
产品描述

C8-D30 [Astrocyte type III clone]细胞

生长状态: 贴壁生长

运输方式: 冻存运输

是否是肿瘤细胞: 0

物种来源: 小鼠

品系: C57BL/6

ATCC Number: CRL-2534™

组织来源: cerebellum

年限: 8 days

数量: 大量

细胞形态: 神经元

器官来源: 大脑

C8-D30 [Astrocyte type III clone]细胞Designations: C8-D30 [Astrocyte type III clone]

Depositors: B Pessac, D Trisler

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Mus musculus deposited as mouse

Morphology: neuronal


Source: Strain: C57BL/6

Organ: brain

Tissue: cerebellum

Permits/Forms: In addition to the MTA mentioned above, other ATCC and/or regulatory permits may be required for the transfer of this ATCC material. C8-D30 [Astrocyte type III clone]细胞Anyone purchasing ATCC material is ultimately responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.

Cytogenetic Analysis: heteroploid [48963]

Age: 8 days

Comments: Clonal permanent cell lines with astrocytic or microglial properties have been established from explant cultures of 8-day postnatal mouse cerebella after in vitro spontaneous transformation. [48963] [49701]

Sister flasks of lethally irradiated astrocytes, which are known to synthesize the macrophage-microglia growth factor, M-CSF, were used as a substrate for cloning the cells. [49701] [48963]

The cell lines were derived in a multistage process. Slowly proliferating foci with several morphologies appeared 4 months after initiation of the cultures and became progressively enriched by cells with a homogeneous appearance. [48963]

Some of these cloned cell lines bound anti-glial fibrillary acidic protein (GFAP) antibodies and therefore appeared to be astrocytic. No other glial neuronal or microglial markers have been detected in these clones. [48963]

According to their morphology, 3 separate types of these GFAP-positive clones could be distinguished. Type I and II cells had small somata. [48963]

Type I had several short processes, while type II had two processes, one of which was very thin and long (greater than 200 microns). Type III cells had large flat somata and no processes. [48963]

C8-D30 [Astrocyte type III clone]细胞The astrocyte type I cloned cell line named C8-D1A is available as ATCC CRL-2541 and the astrocyte type II cloned cell line named C8-S is available as ATCC CRL-2535.

One clone with microglial properties named C8-B4 is available as ATCC CRL-2540.

The C8-D30 cell line has a velate protoplasmic morphology.

These astrocytic clones might be the in vitro counterparts of fibrous (type I), or velamentous (type III) astrocytes and of Golgi epithelial cells (type II). [48963]

Propagation: ATCC complete growth medium: Temperature: 37.0°C

Subculturing: Subcultivation Ratio: A subcultivation ratio of 1:4 to 1:6 is recommended

Medium Renewal: Every 2 to 3 days

Remove medium, and rinse with 0.25% trypsin, 0.03% EDTA solution. Remove the solution and add an additional 1 to 2 ml of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37C) until the cells detach.

Add fresh culture medium, aspirate and dispense into new culture flasks.

Preservation: culture medium 95%; DMSO, 5%

Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2002

recommended serum:ATCC 30-2020

References: 48963: Alliot F, Pessac B. Astrocytic cell clones derived from established cultures of 8-day postnatal mouse cerebella. Brain Res. 306: 283-291, 1984. PubMed: 6466977

49701: Alliot F, et al. C8-D30 [Astrocyte type III clone]细胞A spontaneously immortalized mouse microglial cell line expressing CD4. Brain Res. Dev. Brain Res. 95: 140-143, 1996. PubMed: 8873987

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