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Merck
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主要文件

CTX TNA2

NOTE: Both the cell line and DNA from the cell line may be available for this product. Please choose -1VL or VIAL for cells, or -DNA-5UG for DNA, 98102213, rat brain, Neuronal (astrocyte)

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About This Item

分類程式碼代碼:
41106514

生物源

rat brain

包裝

tube of 5 μg 98102213-DNA-5UG
pkg of vial of cells 98102213-1VL

增長模式

Adherent

染色體組型

Not specified

形態學

Neuronal (astrocyte)

產品

Alpha 2 macroglobulin

受體

Not specified

技術

cell culture | mammalian: suitable

運輸包裝

dry ice

儲存溫度

−196°C

細胞系來源

Rat Astrocyte, Transfected

細胞系描述

Established by transfecting cultures of primary astrocytes from brain frontal cortex tissue of 1 day old sprague-dawley rats with a DNA construct containing the oncogenic early region of SV40. Transcriptional control was effected using the human GFAP promoter (pGFA-SV-TE) and the murine phosphoglycerate kinase promoter (pPGK-neo). Cloning was achieved using G418. The cells are phenotypically similar to type 1 astrocytes. CTX TNA2 displays 20% positive staining for glial fibrillary acid protein (GFAP) and a β alanine inhibitable high affinity uptake mechanism for gamma amino butyric acid (GABA). α-2-macroglobulin production is similar to that found in primary astrocytes, but transferrin production is reduced. The cell line has been shown not to produce proenkephalin A, galactoceebroside or to express the 04 or A2B5 epitopes characteristic of type 2 astrocytes. Immunostaining has shown the SV40 T antigen to be present in over 95% of cells.

應用

Studies of the development and biochemistry of the central nervous system.

培養基

DMEM + 2mM Glutamine + 1mM Sodium Pyruvate (NaP) + 10% Foetal Bovine Serum (FBS).

例行更新培養

Split sub-confluent cultures (70-80%) 1:2 to 1:8 using 0.25% trypsin or trypsin/EDTA; 5% CO2; 37°C. Subculture before flasks become confluent or cells will detach in sheets reducing the effectiveness of trypsin

其他說明

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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