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NCI-H446
Tissue
肺
Disease
肺小細胞癌
Metastatic site
胸腔積液
Synonyms
NCI-H446, H-446, NCI-446, NCIH446

Documents

NCI-H446

Cell line · Product number 305049

This cell line was established in 1982 by D. Carney, A.F. Gazdar and associates from the pleural fluid of a patient with small cell cancer of the lung. The o...

US$395.00excl. tax and shipping
In stock
Lot
Recommended (freshest lot)
  • CoA
1

01General information

Description
該細胞系由 D. Carney、A.F. Gazdar 及其同事於 1982 年從一名小細胞肺癌患者的胸腔積液中建立。 原始腫瘤的形態並無小細胞肺癌的典型特徵。該細胞系在生化特性與形態學上屬於小細胞肺癌的變異型,並會表達神經特異性烯醇化酶以及肌酸激酶的腦型同工酶。 在該細胞系中,未檢測到 L-多巴脫羧酶、邦貝辛、加壓素、催產素或胃泌素釋放肽。該細胞系的 c-myc DNA 擴增程度高出 20 倍,c-myc RNA 水平則高出 15 倍。 該細胞株最初是在無血清的 RPMI 1640 培養基中培養,該培養基中添加了 10 nM 氫化可的松、5 微克/mL 胰島素、10 微克/mL 轉鐵蛋白、10 nM 17-β-雌二醇, 以及 30 nM 亞硒酸鈉。該細胞可形成具有非典型小細胞肺癌組織學特徵的可移植腫瘤。
Tissue
肺
Disease
肺小細胞癌
Metastatic site
胸腔積液
Synonyms
  • NCI-H446
  • H-446
  • NCI-446
  • NCIH446

02Classification

Organism
Human
Sex
Male
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
上皮樣
Tumourigenic
是的,在裸鼠身上(這些細胞會形成具有非典型小細胞肺癌(SCLC)組織學特徵的可移植腫瘤)。

04Identifiers

Citation
NCI-H446(Cytion 型號 305049)
NCBI TaxID
9606
Cellosaurus
CVCL_1562

05Handling and culture

Culture medium
RPMI 1640,含 2.0 mM 穩定谷氨醯胺,含 2.0 g/L NaHCO₃(Cytion 產品編號 820700a)
Incubation atmosphere

37°C,5% CO₂,加濕環境。

Supplements
在培養基中加入 10% FBS,並添加 2.5 g/L 葡萄糖、10 mM HEPES 及 1.0 mM 丙酮酸鈉
Dissociation reagent
Accutase
Subculturing
將懸浮細胞收集至 15 毫升試管中,並用不含鈣和鎂的 PBS 輕柔地洗滌貼壁細胞(T25 培養瓶使用 3-5 毫升,T75 培養瓶使用 5-10 毫升)。 加入 Accutase(T25 培養瓶使用 1–2 毫升,T75 培養瓶使用 2.5 毫升),確保完全覆蓋細胞層。讓細胞於室溫下孵育 10 分鐘。 孵育完成後,將懸浮細胞與貼壁細胞合併並進行離心。離心後,小心地將細胞沉澱重新懸浮,並將細胞懸液轉移至裝有新鮮培養基的新培養瓶中。
Fluid renewal
每週 2 至 3 次
Thawing and culturing
  1. Confirm that the vial remains deeply frozen upon delivery, as cells are shipped on dry ice to maintain optimal temperatures during transit.

  2. Upon receipt, either store the cryovial immediately at temperatures below -150°C to ensure the preservation of cellular integrity, or proceed to step 3 if immediate culturing is required.

  3. For immediate culturing, swiftly thaw the vial by immersing it in a 37°C water bath with clean water and an antimicrobial agent, agitating gently for 40-60 seconds until a small ice clump remains.

  4. Perform all subsequent steps under sterile conditions in a flow hood, disinfecting the cryovial with 70% ethanol before opening.

  5. Carefully open the disinfected vial and transfer the cell suspension into a 15 ml centrifuge tube containing 8 ml of room-temperature culture medium, mixing gently.

  6. Centrifuge the mixture at 300 x g for 3 minutes to separate the cells and carefully discard the supernatant containing residual freezing medium.

  7. Gently resuspend the cell pellet in 10 ml of fresh culture medium. For adherent cells, divide the suspension between two T25 culture flasks; for suspension cultures, transfer all the medium into one T25 flask to promote effective cell interaction and growth.

  8. Adhere to established subculture protocols for continued growth and maintenance of the cell line, ensuring reliable experimental outcomes.

06Quality control and cryopreservation

Sterility

透過基於 PCR 的檢測及基於發光原理的支原體檢測方法,排除支原體污染的可能性。

為確保無細菌、真菌或酵母菌污染,每日均會對細胞培養物進行目視檢查。

Freeze medium
作為冷凍保存培養基,我們使用完全生長培養基(含 FBS)+ 10% DMSO 以確保解凍後的存活率,或使用 CM-1 (Cytion 型號 800100),該培養基含有經優化的滲透保護劑和代謝穩定劑,可提升細胞恢復率並減輕冷凍誘導的壓力。
Storage conditions

若需長期保存,請將試管置於溫度約為 −150 至 −196 °C 的氣相液氮中。僅在轉移至液氮之前,可將試管暫時存放於 −80 °C 環境中,作為短期過渡步驟。

Shipping conditions

冷凍保存的細胞系會以乾冰冷藏,並裝於經驗證的隔熱包裝中,包裝內含有足夠的冷媒,以確保在運輸過程中溫度維持在約 −78 °C。收到貨物後,請立即檢查容器,並盡快將試管轉移至適當的儲存場所。

07Donor

Donor age
61年
Ethnicity
歐洲的