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產品資料

PC-12 Adh細胞

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產品名稱: PC-12 Adh細胞
產品型號: PC-12 Adh
產品展商: HZbscience
產品文檔: 無相關文檔

簡單介紹

PC-12 Adh細胞應如何避免細胞污染,細胞污染的種類可分成**、酵母菌、霉菌、病毒和霉?jié){菌。主要的污染原因為無菌操作技術不當、操作室環(huán)境不佳、污染之血清和污染之細胞等。嚴格之無菌操作技術、清潔的環(huán)境、與品質良好之細胞來源和培養(yǎng)基配制是減低污染之*好方法。PC-12 Adh細胞何時須更換培養(yǎng)基?視細胞生長密度而定,或遵照細胞株基本數據上之更換時間,按時更換培養(yǎng)基即可。


PC-12 Adh細胞  的詳細介紹

PC-12 Adh細胞

細胞形態(tài): 多邊形

運輸方式: 凍存運輸

是否是腫瘤細胞: 0

物種來源: 大鼠

生長狀態(tài): 貼壁生長

數量: 大量

ATCC Number: CRL-1721.1?

相關**: 其他**

器官來源: 腎上腺

Designations: PC-12 Adh

Depositors: B Patterson

PC-12 Adh細胞Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent, small clusters

Organism: Rattus norvegicus deposited as Rattus sp.

Morphology: polygonal


Source: Organ: adrenal gland

Disease: pheochromocytoma

Cellular Products: catecholamines; dopamine; norepinephrine [1163]

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. 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.

Applications: transfection host

Tumorigenic: Yes

Cytogenetic Analysis: 40 chromosomes; 38 autosomes plus XY [1163]

Gender: PC-12 Adh細胞male

Comments: The PC-12 cell line was derived from a transplantable rat pheochromocytoma. The cells do not synthesize epinephrine. This adherent variant (PC-12 Adh) has been adapted to Corning CellBIND&reg flasks to improve cell attachment.

Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated F-12K Medium, Catalog No. 30-2004. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 2.5%; horse serum to a final concentration of 15%.

Atmosphere: air, 95%; carbon dioxide (CO2), 5%

Temperature: 37.0°C

Subculturing: Protocol: Volumes used for this protocol are for a 75cm2 flask; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes.

Remove and discard old culture medium.

Pipet 10 ml fresh medium over the cell sheet and scrape.

Aspirate cells with a small bore pipette to break up clusters.

Add appropriate aliquots of the cell suspension to new Corning CellBIND&reg 75 cm2 flask with 15 ml fresh growth medium. Seed flask at 1.0 x 10(4) to 3.0x 10(4) viable cells / cm2 or use subcultivation ratio of 1:3 twice weekly.Subculture when cell density reaches between 1.0x 1 0(5) to 2.0x 10(5) viable cells / cm2.

Place culture vessels in incubator at 37?C.


Medium Renewal: Every 2 to 3 days

Preservation:PC-12 Adh細胞Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO

Storage temperature: liquid nitrogen vapor phase

Doubling Time: 48 hrs

Related Products: Parent cell line: CRL-1721, PC-12

Recommended medium (without the additional supplements or serum described under ATCC Medium): ATCC 30-2004

recommended serum: ATCC 30-2020

recommended serum: ATCC 30-2040

References: 1162: Levi A, et al. Molecular cloning of a gene sequence regulated by nerve growth factor. Science 229: 393-395, 1985. PubMed: 3839317

1163: Greene LA, Tischler AS. Establishment of a noradrenergic clonal line of rat adrenal pheochromocytoma cells which respond to nerve growth factor. Proc. Natl. Acad. Sci. USA 73: 2424-2428, 1976. PubMed: 1065897

22344: Biocca S, et al. A macromolecular structure favouring microtubule assembly in NGF- differentiated pheochromocytoma cells (PC12). EMBO J. 2: 643-648, 1983. PubMed: 6641712

33014: Weber E, et al. PC-12 Adh細胞Distinct functional properties of Rab3A and Rab3B in PC12 neuroendocrine cells. J. Biol. Chem. 271: 6963-6971, 1996. PubMed: 8636125

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