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CRL-1711 SF9 昆蟲卵巢細胞

簡要描述:CRL-1711 SF9 昆(kun)蟲卵(luan)巢細(xi)(xi)胞(bao)(bao),ATCC 細(xi)(xi)胞(bao)(bao)|細(xi)(xi)胞(bao)(bao)系|細(xi)(xi)胞(bao)(bao)株(zhu)|腫瘤細(xi)(xi)胞(bao)(bao)|細(xi)(xi)胞(bao)(bao)|貼壁(bi)細(xi)(xi)胞(bao)(bao)|懸浮細(xi)(xi)胞(bao)(bao)|,細(xi)(xi)胞(bao)(bao)庫管理規范,提(ti)供的細(xi)(xi)胞(bao)(bao)株(zhu)背景清(qing)楚,提(ti)供參考文(wen)獻(xian)和*培養條(tiao)件(jian)

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CRL-1711 SF9 昆蟲卵巢細胞,ATCC 細胞|細胞系|細胞株|腫瘤細胞|細胞|貼壁細胞|懸浮細胞|,細胞庫管理規范,提供的細胞株背景清楚,提供參考文獻優培養條件


CRL-1711 SF9 昆蟲卵巢細胞 的詳細介紹


ATCC® Number: CRL-1711™    Price: $275.00
Designations: Sf9

Depositors: G Smith, C Cherry, MD Summers

Biosafety Level:1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties:mixed: adherent/suspension

Organism:Spodoptera frugiperda (fall armyworm)

Morphology:epithelial
<strong><strong><strong><strong><strong><strong><strong><strong><strong><strong><strong><strong><strong><strong><strong><strong><strong><strong></strong></strong></strong></strong></strong></strong></strong></strong></strong></strong></strong></strong></strong></strong></strong></strong></strong></strong>


Source:Organ: ovary

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 ultimay responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.


Isolation: Isolation date: 1983

Applications:transfection host (Roche FuGENE® Transfection Reagents

technology from amaxa)



Virus Susceptibility:Nuclear polyhedrosis virus, Autographa californica

St. Louis encephalitis virus



Age: pupa

Gender: female

Comments:This line can be used to replicate baculovirus expression vectors.

It is important to use the medium described below.



Propagation: ATCC complete growth medium: Grace's Insect Medium with L-glutamine and supplemented with:

500 mg/L calcium chloride

2800 mg/L potassium chloride

3330 mg/L lactalbumin hydrolysate

3330 mg/L yeastolate

10% Heat-inactivated fetal bovine serum (previously tested for insect cell culture)


Atmosphere: air, 100%
Temperature: 28.0°C
Growth Conditions: The recommended media are formulated for use without CO2. Omission of the yeastolate or lactalbumin hydrolysate will lead to poor performance by this line.


Subculturing: Protocol: Gently resuspend cells in the spent culture medium by pipetting across the monolayer or by hitting the flask against the palm of your hand (the latter is only preferable when working with larger flasks).
Subc*tion Ratio: A subc*tion ratio of 1:5 or greater is recommended
Medium Renewal: Every 2 to 3 days


Preservation: Freeze medium: culture medium, 95%; DMSO, 5%
Storage temperature: liquid nitrogen vapor phase


References:22650: Vaughn JL, et al. The establishment of two cell lines from the insect Spodoptera frugiperda (Lepidoptera; Noctuidae). In Vitro 13: 213-217, 1977. PubMed: 68913

23136: Zhang PF, et al. Susceptibility of the Sf9 insect cell line to infection with adventitious viruses. Biologicals 22: 205-213, 1994. PubMed: 7811453

23294: Smith GE, et al. Modification and secretion of human interleukin 2 produced in insect cells by a baculovirus expression vector. Proc. Natl. Acad. Sci. USA 82: 8404-8408, 1985. PubMed: 3878519

32359: Hall MR, Gibson W. Cytomegalovirus assemblin: the amino and carboxyl domains of the proteinase form active enzym e when separay cloned and coexpressed in eukaryotic cells. J. Virol. 70: 5395-5404, 1996. PubMed: 8764050

32361: Bakker A, et al. Human T-cell leukemia virus type 2 Rex inhibits pre-mRNA splicing in vitro at an early stage of spliceosome formation. J. Virol. 70: 5511-5518, 1996. PubMed: 8764063

32693: Gibson W, et al. Cytomegalovirus "missing" capsid protein identified as heat-aggregable product of human cytomegalovirus UL46. J. Virol. 70: 7454-7461, 1996. PubMed: 8892863

32860: Filtz TM, et al. Purification and G protein subunit regulation of a phospholipase C-beta from Xenopus laevis oocytes. J. Biol. Chem. 49: 31121-31126, 1996. PubMed: 8940109

32882: Lindorfer MA, et al. G protein gamma subunits with altered prenylation sequences are properly modified when expressed in Sf9 cells. J. Biol. Chem. 271: 18582-18587, 1996. PubMed: 8702508

33023: Bruant SS, et al. N-terminal sequences contained in the Src homology 2 qand 3 domains of p120 GTPase-activating protein are required for full catalytic activity toward ras. J. Biol. Chem. 271: 5195-5199, 1996. PubMed: 8617802

33034: Stewart L, et al. Biochemical and biophysical analyses of recombinant forms of human topoisomerase I. J. Biol. Chem. 271: 7593-7601, 1996. PubMed: 8631793

33143: Kawabe J, et al. Soluble adenylyl cyclase from Spodoptera frugiperda (Sf9) cells. J. Biol. Chem. 271: 20132-20137, 1996. PubMed: 8702736

33160: Yasuda H, et al. Role of the prenyl group on the G protein gamma subunit in coupling trimeric G proteins to A1 adenosine receptors. J. Biol. Chem. 271: 18588-18595, 1996. PubMed: 8702509

















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