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平臺編號：bio-69707
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細(xì)胞信息： HH-8
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規(guī)格：1×10?cells/T25培養(yǎng)瓶
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用途：/
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服務(wù)費用：
加載中…… - 訂購
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注意事項：僅用于科學(xué)研究或者工業(yè)應(yīng)用等非醫(yī)療目的不可用于人類或動物的臨床診斷或治療，非藥用，非食用（產(chǎn)品信息以出庫為準(zhǔn)）
人胚腎細(xì)胞
HH-8人胚腎細(xì)胞
產(chǎn)品類別：人源細(xì)胞系
生長特性：貼壁生長
細(xì)胞形態(tài)：N/A
凍存條件：90%FBS+10%DMSO
Synonyms: HH-8人胚腎細(xì)胞
Background: The cell line HH-8 was generated by transfecting a vector (pcDNA3) containing a truncated calcium channel cDNA into (HEK) 293 cells (ECACC catalogue no. 85120602). The vector is constituitively expressed in the HH-8 cells producing a truncated (at amino acid 1733) cardiac alpha 1c-a calcium channel.
Species: human (Homo sapiens)
Tissue: Kidney, embryo
Disease: Human embryo kidney
Gender: N/A
GMO Status: Genetically Modified Organism Class 1 (GMO1)
Growth Mode: Semi-adherent aggregates
Doubling Time: N/A
DNA Profile: Cell Line Authentication Service
Culture Medium: DMEM+10%FBS
We strongly suggest to purchase the complete medium
Cryopreservation medium: 90%FBS+10%DMSO
Karyotype: Not specified
Subculture Routine: Split sub-confluent cultures (70-80%) 1:2 to 1:3 i.e. seeding at 3-5x10,000 cells/cm2 using 0.25% trypsin, trypsin/EDTA, or PBS wash, 5% CO2; 37°C. Cells may take up to 7 days to attach after resuscitation and sub culture. Cells grow in large aggregates that do not grow to confluency. Cells detach easily at room temperature or during transit, therefore growing cultures may be received with cells in suspension. In this event, centrifuge contents of flask and re-seed to allow re-attachment of cells.
產(chǎn)品類別：人源細(xì)胞系
生長特性：貼壁生長
細(xì)胞形態(tài)：N/A
凍存條件：90%FBS+10%DMSO
Synonyms: HH-8人胚腎細(xì)胞
Background: The cell line HH-8 was generated by transfecting a vector (pcDNA3) containing a truncated calcium channel cDNA into (HEK) 293 cells (ECACC catalogue no. 85120602). The vector is constituitively expressed in the HH-8 cells producing a truncated (at amino acid 1733) cardiac alpha 1c-a calcium channel.
Species: human (Homo sapiens)
Tissue: Kidney, embryo
Disease: Human embryo kidney
Gender: N/A
GMO Status: Genetically Modified Organism Class 1 (GMO1)
Growth Mode: Semi-adherent aggregates
Doubling Time: N/A
DNA Profile: Cell Line Authentication Service
Culture Medium: DMEM+10%FBS
We strongly suggest to purchase the complete medium
Cryopreservation medium: 90%FBS+10%DMSO
Karyotype: Not specified
Subculture Routine: Split sub-confluent cultures (70-80%) 1:2 to 1:3 i.e. seeding at 3-5x10,000 cells/cm2 using 0.25% trypsin, trypsin/EDTA, or PBS wash, 5% CO2; 37°C. Cells may take up to 7 days to attach after resuscitation and sub culture. Cells grow in large aggregates that do not grow to confluency. Cells detach easily at room temperature or during transit, therefore growing cultures may be received with cells in suspension. In this event, centrifuge contents of flask and re-seed to allow re-attachment of cells.
