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S42細(xì)胞

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產(chǎn)品名稱: S42細(xì)胞
產(chǎn)品型號(hào): S42
產(chǎn)品展商: HZbscience
產(chǎn)品文檔: 無相關(guān)文檔

簡(jiǎn)單介紹

S42細(xì)胞應(yīng)如何避免細(xì)胞污染,細(xì)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?yàn)闊o菌操作技術(shù)不當(dāng)、操作室環(huán)境不佳、污染之血清和污染之細(xì)胞等。嚴(yán)格之無菌操作技術(shù)、清潔的環(huán)境、與品質(zhì)良好之細(xì)胞來源和培養(yǎng)基配制是減低污染之*好方法。S42細(xì)胞何時(shí)須更換培養(yǎng)基?視細(xì)胞生長(zhǎng)密度而定,或遵照細(xì)胞株基本數(shù)據(jù)上之更換時(shí)間,按時(shí)更換培養(yǎng)基即可。


S42細(xì)胞  的詳細(xì)介紹

S42細(xì)胞

生長(zhǎng)狀態(tài): 貼壁生長(zhǎng)

細(xì)胞類型: 其他細(xì)胞類型

數(shù)量: 大量

是否是腫瘤細(xì)胞: 0

物種來源: 褐鼠

年限: neonatal

運(yùn)輸方式: 凍存運(yùn)輸

組織來源: sciatic nerve

ATCC Number: CRL-2942?

細(xì)胞形態(tài): 上皮樣

Designations: S42

Depositors: RH Quarles

S42細(xì)胞Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Rattus norvegicus

Morphology: epithelial-like


Source: Tissue: sciatic nerve

Cell Type: Schwann cell

Cellular Products: laminin

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.

Isolation: Isolation date: 1989

Antigen Expression: Myelin-associated glycoprotein (MAG)

Galactocerebroside (GalC)

Age: neonatal

Comments: S42細(xì)胞The S42 cell line is derived from a primary culture of Schwann cells that was immortalized by repetitive passaging. S42 is similar to S16 (ATCC CRL-2941), but it has a higher level of High Myelin-associated glycoprotein (MAG) and a longer doubling time. At high density, the S42 cells exhibit numerous processes. Both S42 and S16 cells express galactocerebroside (GalC), sulfatide and P0 glycoprotein, but little or no myelin basic protein. [16172655] [16172656]

In many respects, S42 (ATCC CRL-2942) and S16 (ATCC CRL-2941) resemble Schwann cells at an early stage in their preparation to myelinate and are useful for investigating the cell biology of MAG and other myelin-related components. [16172656]

Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.

Temperature: 37.0°C

Subculturing: Protocol: The culture flasks should be treated with 0.1ml/sq. cm of flask surface area with 15ug/ml poly-L-lysine (Sigma Cat. No. P-9155 or equivalent) for at least 2 hours at 37°C. Remove solution and rinse one time with DPBS and allow flask to air dry uncapped and standing upright in a biological cabinet for about 30 minutes before introducing cells.

Volumes used in this protocol are for 75 sq. cm flasks; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes.

Remove and discard culture medium.

Briefly rinse the cell layer with Ca++/Mg++ free Dulbecco's phosphate-buffered saline (DPBS) or 0.25% (w/v) Trypsin - 0.53 mM EDTA solution to remove all traces of serum which contains trypsin inhibitor.

Add 2.0 to 3.0 ml of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).

Note: S42細(xì)胞To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37°C to facilitate dispersal.

Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting.

Transfer cell suspension to a centrifuge tube and spin at approximately 125 xg for 5 to 10 minutes. Discard supernatant.

Resuspend the cell pellet in fresh growth medium. Add appropriate aliquots of the cell suspension to new culture vessels. An inoculum of 2 X 10(4) to 4 X 10(4) viable cells/sq. cm is recommended.

Incubate cultures at 37°C. We recommend that you subculture cultures when they reach a cell concentration between 1 X 10(5) and 2 X 10(5) cells/sq. cm.

Subcultivation ratio: A subcultivation ratio of 1:3 to 1:6 twice weekly is recommended.

Medium renewal: Every 2 to 3 days

Preservation: Freeze medium: complete growth medium, 90%; DMSO, 10%

Storage temperature: liquid nitrogen vapor phase

Doubling Time: approximately 48 hours [16172656]

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

Recommended serum: ATCC 30-2020

0.25% (w/v) Trypsin - 0.53mM EDTA in Hank's BSS (w/o Ca++, Mg ++): ATCC 30-2101

Phosphate-buffered saline: ATCC 30-2200

Cell culture tested DMSO: ATCC 4-X

Erythrosin B vital stain solution: ATCC 30-2404

CRL-2944 (B11F7) Myelin-associated glycoprotein (MAG) antibody producing cell line

CRL-2941 (S16) Rat Schwann cells

CRL-2943 (S16Y) Rat Schwann cells

References: 16172655: Goda S, et al. Expression of the myelin-associated glycoprotein in cultures of immortalized Schwann cells. J. Neurochem. 56(4):1354-1361, 1991. PubMed: 1705958

16172656: Toda K, et al. S42細(xì)胞Biochemical and cellular properties of three immortalized Schwann cell lines expressing different levels of the myelin-associated glycoprotein. J. Neurochem. 63(5):1646-1657, 1994. PubMed: 7523597

16172657: Sasagasako N, et al. Myelin gene expression in immortalized Schwann cells: relationship to cell density and proliferation. J. Neurochem. 66(4): 1432-1439, 1996. PubMed: 8627295

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