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平臺編號：bio-132806
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細(xì)胞信息： PE/CA-PJ15
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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(fèi)用：
加載中…… - 訂購
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注意事項(xiàng)：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)）
PE/CA-PJ15（人口腔鱗狀細(xì)胞癌）
PE/CA-PJ15（人口腔鱗狀細(xì)胞癌）
產(chǎn)品類別：人源細(xì)胞系
細(xì)胞形態(tài)：Epithelial-like
凍存條件：90%FBS+10%DMSO
Synonyms:PE/CA-PJ15
Background:The cell line PE/CA-PJ15 was established from tongue tissue of a 45 year old male patient with oral squamous cell carcinoma. The cells have been shown to have epithelial differentiated characteristics expressing laminin and cytokeratins. Involucrin has been detected in some cells and cell groups.
Species:human (Homo sapiens)
Tissue:Tongue epithelium
Disease:Human oral squamous cell carcinoma
Gender:45 year old male
Morphology:Epithelial-like
Growth Mode:Adherent
Doubling Time:N/A
DNA Profile: Cell Line Authentication Service
Culture Medium:IMDM+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 1:8 using 0.25% trypsin or trypsin/EDTA; 5% CO2; 37°C. Note: cells may take up to 7 days to become confluent, a medium change during this period may be required.
產(chǎn)品類別：人源細(xì)胞系
細(xì)胞形態(tài)：Epithelial-like
凍存條件：90%FBS+10%DMSO
Synonyms:PE/CA-PJ15
Background:The cell line PE/CA-PJ15 was established from tongue tissue of a 45 year old male patient with oral squamous cell carcinoma. The cells have been shown to have epithelial differentiated characteristics expressing laminin and cytokeratins. Involucrin has been detected in some cells and cell groups.
Species:human (Homo sapiens)
Tissue:Tongue epithelium
Disease:Human oral squamous cell carcinoma
Gender:45 year old male
Morphology:Epithelial-like
Growth Mode:Adherent
Doubling Time:N/A
DNA Profile: Cell Line Authentication Service
Culture Medium:IMDM+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 1:8 using 0.25% trypsin or trypsin/EDTA; 5% CO2; 37°C. Note: cells may take up to 7 days to become confluent, a medium change during this period may be required.
