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MA-891
Tissue
乳腺
Disease
癌
Metastatic site
轉移性(高度轉移潛能;主要轉移至肺部)
Synonyms
Mouse Mammary Carcinoma Highly Metastatic Cell Line

Documents

MA-891

Cell line · Product number 305581

MA-891 is a highly metastatic murine mammary gland carcinoma cell line, established from a spontaneous mammary tumor in a mouse and selected for its aggre...

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1

01General information

Description

MA-891 是一種高度轉移性的小鼠乳腺癌細胞系,源自一隻小鼠體內的自發性乳腺腫瘤,並因其具侵略性的轉移行為而經篩選建立。 該細胞系以黏附性單層形式生長,被歸類為與免疫功能正常小鼠宿主相容的同基因腫瘤細胞系,可藉此進行乳腺癌生長、轉移及免疫相互作用的體內研究。 MA-891 是一種高度轉移性的變異株,因其易於擴散至遠端器官(尤其是肺部)而被篩選出來。

MA-891 適用於小鼠乳腺癌研究,包括轉移級聯生物學、侵襲、血管生成、腫瘤-免疫相互作用的研究,以及抗轉移和抗腫瘤藥物的臨床前評估。 其同基因源特性,使其能夠在免疫功能正常的宿主中測試免疫療法,包括檢查點抑制劑的評估及癌症疫苗的開發。其高度的轉移潛力,使其成為研究轉移預防策略及侵襲性乳腺癌生物學的有用模型。

Tissue
乳腺
Disease
癌
Metastatic site
轉移性(高度轉移潛能;主要轉移至肺部)
Applications
小鼠乳腺癌研究;轉移生物學;抗轉移藥物評估;同基因型腫瘤免疫療法;腫瘤與免疫系統的相互作用;癌症疫苗研究
Synonyms
  • Mouse Mammary Carcinoma Highly Metastatic Cell Line

02Classification

Organism
Mouse
Sex
Female
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
上皮樣
Cell type
腫瘤細胞系
Doubling time
約 18 至 24 小時

04Identifiers

Citation
MA-891(Cytion 型號 305581)
NCBI TaxID
10090

05Handling and culture

Culture medium
含 10% 胎牛血清 (FBS) 的 RPMI-1640 培養基;1% 青黴素-鏈黴素溶液
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)及 1% 的青黴素-鏈黴素
Dissociation reagent
Accutase
Subculturing
移除培養基,用不含鈣和鎂的PBS清洗,加入Accutase覆蓋,於室溫下孵育 8–10 分鐘,重新懸浮於培養基中,以 300×g 離心 3 分鐘,棄去上清液,再將細胞接種於新鮮培養基中。
Split ratio
1 至 5
Seeding density
1 至 3 × 10⁴ 個細胞/cm²
Fluid renewal
每 2 至 3 天
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

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
年齡不詳
Ethnicity
未指定