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AH-130
Tissue
肝臟
Disease
肝細胞癌
Metastatic site
腹水
Synonyms
Yoshida AH-130, Yoshida AH130, AH130, AH 130, AH-130 Yoshida, AH130-TC, AH130/P

Documents

AH-130

Cell line · Product number 500412

Yoshida et al. have established the ascites hepatoma by converting the aminoazo dyeinduced hepatoma of the rat into the ascetic form (Yoshida 1956). AH-130 i...

US$800.00excl. tax and shipping
In stock
Lot
Recommended (freshest lot)
  • CoA
1

01General information

Description
吉田等人透過將大鼠的氨基偶氮染料誘導性肝癌轉化為腹水型,成功建立了腹水性肝癌模型(Yoshida 1956)。 AH-130 是一種由游離腫瘤細胞組成的腹水肝癌株,其中僅存在少量腫瘤島。本文所述的細胞系,即是以此吉田 AH-130 腹水肝癌株為基礎,透過體外細胞培養所建立的。
Tissue
肝臟
Disease
肝細胞癌
Metastatic site
腹水
Applications
肝細胞癌研究;大鼠肝腫瘤生物學;吉田腹水肝癌模型;藥物敏感性與細胞毒性測試;腺病毒易感性研究;斯普拉格-道利大鼠的肝癌臨床前模型建立;黏附性/懸浮性腫瘤生物學
Synonyms
  • Yoshida AH-130
  • Yoshida AH130
  • AH130
  • AH 130
  • AH-130 Yoshida
  • AH130-TC
  • AH130/P

02Classification

Organism
Rat
Sex
Unspecified
Growth properties
Adherent and suspension
GMO status
Non-GMO
GMO status details
No genetic modification; transplantable rat ascites hepatoma derived from aminoazo dye-induced primary hepatoma by Yoshida (1956)
Biosafety level
1

03Characteristics

Morphology
圓形懸浮細胞、三角形貼壁細胞
Cell type
肝細胞癌細胞(肝癌)
Tumourigenic
是的,在 Wistar 及其他品系中皆是如此。
Doubling time
約 18 至 24 小時(生長迅速;BD=已確認為快速型)

04Identifiers

Citation
AH-130(Cytion 型號 500412)
NCBI TaxID
10116
Cellosaurus
CVCL_4367

05Expression and susceptibility

Viruses
RAP 檢測結果為陰性。 .
Virus susceptibility
對人類腺病毒極為敏感

06Handling and culture

Culture medium
DMEM:Ham's F12(1:1),重量比:3.1 g/L 葡萄糖,重量比:2.5 mM L-谷氨酰胺,重量比:15 mM HEPES, w: 0.5 mM 丙酮酸鈉,w: 1.2 g/L NaHCO₃(Cytion 產品編號 820400a)
Incubation atmosphere

37°C,5% CO₂,加濕環境。

Supplements
在培養基中加入 10% 的胎牛血清(FBS)
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。
Split ratio
1 至 3
Seeding density
2 × 10⁴ 個細胞/cm²
Fluid renewal
每 3 至 5 天
Post-thaw recovery
快速
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.

07Quality 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。

08Donor

Breed / subspecies
斯普拉格-道利
Donor age
年齡不詳
Ethnicity
不適用(大鼠細胞系;Q 項為斯普拉格-道利大鼠)