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RPE-J細(xì)胞

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產(chǎn)品名稱(chēng): RPE-J細(xì)胞
產(chǎn)品型號(hào): RPE-J
產(chǎn)品展商: HZbscience
產(chǎn)品文檔: 無(wú)相關(guān)文檔

簡(jiǎn)單介紹

RPE-J細(xì)胞應(yīng)如何避免細(xì)胞污染,細(xì)胞污染的種類(lèi)可分成**、酵母菌、霉菌、病毒和霉?jié){菌。主要的污染原因?yàn)闊o(wú)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(wú)菌操作技術(shù)、清潔的環(huán)境、與品質(zhì)良好之細(xì)胞來(lái)源和培養(yǎng)基配制是減低污染之*好方法。RPE-J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。


RPE-J細(xì)胞  的詳細(xì)介紹

RPE-J細(xì)胞

數(shù)量: 大量

器官來(lái)源: 眼

年限: 7 days

生長(zhǎng)狀態(tài): 貼壁生長(zhǎng)

細(xì)胞形態(tài): 上皮樣

組織來(lái)源: retinal pigmented epithelium; retina

相關(guān)**: 正常

ATCC Number: CRL-2240?

品系: Long-Evans

物種來(lái)源: 大鼠

是否是腫瘤細(xì)胞: 0

細(xì)胞類(lèi)型: 其他細(xì)胞類(lèi)型

運(yùn)輸方式: 凍存運(yùn)輸

RPE-J細(xì)胞Designations: RPE-J

Depositors: E Rodriquez-Boulan

Biosafety Level: 2 [Papovavirus (cells contain SV-40 virus) ]

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Rattus norvegicus deposited as Rattus sp.

Morphology: epithelial


Source: Organ: eye

Strain: Long-Evans

Tissue: retinal pigmented epithelium; retina

Disease: normal

Cell Type: epithelialSV40 transformed

Cellular Products: SV40 T antigen

tight junction protein 1 (zona occludens 1)

Permits/Forms: RPE-J細(xì)胞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.

Tumorigenic: No

Age: 7 days

Comments: RPE-J is a retinal pigment epithelial (RPE) cell line derived from primary cultures of RPE cells taken from 7-day-old Long-Evans rats. The cells were transformed at 33C with the temperature-sensitive tsA SV40 virus, and cloned by limiting dilution. The RPE-J clone was selected for an epithelioid morphology and for expression of circumferential staining with antibody against the tight junction protein 1, (Tjp1, ZO-1).

The cells express a transformed phenotype at the permissive temperature (33C), and a non-transformed phenotype at the non-permissive temperature (40C). They must be cultured at the permissive temperature and do not grow at 37C.

When RPE-J cells are grown on nitrocellulose filters coated with a thin layer of Matrigel in the presence of 10(-8) M retinoic acid for 6 days at 33C and then switched to the non-permissive temperature of 40C for 33 to 36 hours, they acquire a differentiated polarized RPE phenotype. Under these conditions, RPE-J cells exhibit circumferential staining for the tight-junction protein ZO-1 and acquire a transepithelial resistance of 350 ohms/cm2 [PubMed ID: 8383696].

RPE-J is the only established RPE cell line that maintains epithelial cell surface polarity. The cells retain many properties of RPE including expression of the rat RPE marker RET-PE2 and the ability to phagocytose latex beads [PubMed ID: 8383696].

A culture submitted to the ATCC in July 1995 was found to be contaminated with Mycoplasma hyorhinis and was cured by a 21-day treatment with BM Cycline. RPE-J細(xì)胞The cells were assayed for mycoplasma by the Hoechst stain and the standard culture test over a six-week period following treatment and all tests were negative.

Propagation: ATCC complete growth medium: Dulbecco's modified Eagle's medium with 4 mM L-glutamine adjusted to contain 1.5g/L sodium bicarbonate and 4.5 g/L glucose and supplemented with 0.1 mM non-essential amino acids, 96%; fetal bovine serum, 4%

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

Temperature: 33.0°C

Subculturing: Protocol:

Remove and discard culture medium.

Briefly rinse the cell layer with 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 with 5 to 10 minutes).

Note: 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 37C 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 x g for 5 to 10 minutes. Discard supernatant.

Resuspend the cell pellet in fresh growth medium. Add appropriate aliquots of cell suspension to new culture vessels.

Place culture vessels in incubators at 33C.


Subcultivation Ratio: RPE-J細(xì)胞A subcultivation ratio of 1:3 is recommended

Medium Renewal: Every 2 to 3 days

Preservation: Freeze medium: Complete growth medium with an additional 16% fetal bovine serum and 5% (v/v) DMSO

Storage temperature: liquid nitrogen vapor phase

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

recommended serum:ATCC 30-2020

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

Cell culture tested DMSO:ATCC 4-X

References: 22464: Nabi IR, et al. Immortalization of polarized rat retinal pigment epithelium. J. Cell Sci. 104: 37-49, 1993. PubMed: 8383696

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