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Mx-1
Tissue
乳房
Disease
腺癌,浸潤性導管癌(IDC)
Synonyms
Mx1, MxI

Documents

Mx-1

Cell line · Product number 300296

The Mx-1 cell line has been established as in vitro culture from the Mx-1 tumor xenograft model of breast carcinoma tissue.

US$650.00excl. tax and shipping
In stock
Lot
Recommended (freshest lot)
  • CoA
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1

01General information

Description
Mx-1 細胞系是從 Mx-1 乳腺癌組織腫瘤異種移植模型中,透過體外培養所建立的。
Tissue
乳房
Disease
腺癌,浸潤性導管癌(IDC)
Synonyms
  • Mx1
  • MxI

02Classification

Organism
Human
Sex
Female
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
上皮樣
Tumourigenic
是的,在裸鼠身上
Doubling time
30 至 35 小時

04Identifiers

Citation
Mx-1(Cytion 型號 300296)
NCBI TaxID
9606
Cellosaurus
CVCL_4774

05Expression and susceptibility

Receptors expressed
雌激素(oestrogen)受體(-)
Protein expression
P53 (-)

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
移除培養基,並使用不含鈣和鎂的PBS沖洗貼壁細胞(T25細胞培養瓶需3-5毫升PBS,T75細胞培養瓶需5-10毫升)。 加入 TrypleExpress(T25 培養瓶每瓶 1–2 毫升,T75 培養瓶每瓶 2.5 毫升),務必完全覆蓋細胞片。於 37 攝氏度下孵育 10 分鐘。 小心將細胞重新懸浮,可選擇性添加培養基但非必要,並分裝至含有新鮮培養基的新培養瓶中。切勿讓細胞達到融合狀態,每週進行一次傳代。注意:這些細胞不會形成融合的單層。當肉眼觀察到細胞層密度較高時,即進行傳代。
Seeding density
2 × 10⁴ 個細胞/cm²
Fluid renewal
每週 2 至 3 次
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

Donor age
29年
Ethnicity
高加索人