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P388-D1
Tissue
造血
Disease
淋巴系腫瘤
Synonyms
P-388D1, P388D1, P388.D1, P3 88 D1

Documents

P388-D1

Cell line · Product number 400308

A subclone of this line [P388 D1(IL-1)] produces high levels of interleukin-1 (IL-1).

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

01General information

Description
該細胞系 [P388 D1(IL-1)] 的某個亞克隆能產生高濃度的白細胞介素-1(IL-1)。
Tissue
造血
Disease
淋巴系腫瘤
Synonyms
  • P-388D1
  • P388D1
  • P388.D1
  • P3 88 D1

02Classification

Organism
Mouse
Sex
Female
Growth properties
Suspension
Biosafety level
1

03Characteristics

Morphology
圓形細胞
Cell type
巨噬細胞
Tumourigenic
是的,在裸鼠身上
MSI status
不穩定

04Identifiers

Citation
P388-D1(Cytion 型號 400308)
NCBI TaxID
10090
Cellosaurus
CVCL_0477

05Expression and susceptibility

Antigen expression
H-2d
Viruses
MAP 檢測呈陰性:仙台病毒、Ektromelie(鼠痘)、 多瘤病毒、K 病毒、基爾漢病毒、雷奧 3 型病毒、PVM、LCM、肺型米氏病毒、MVM、泰勒氏 GD VII 病毒、圖蘭 H-1 病毒、MHV、LDV、RCV/SDA、M-腺病毒、B.piliformis。
Reverse transcriptase
正向

06Handling 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% 的胎牛血清(FBS)
Subculturing
透過定期添加或更換培養基來維持培養。以 5 × 10⁵ 細胞/毫升的密度啟動培養,並將細胞濃度維持在 3 × 10⁵ 至 1 × 10⁶ 細胞/毫升的範圍內,以達到最佳生長效果。
Seeding density
以 1 × 10⁶ 個活細胞/毫升的濃度進行傳代培養
Fluid renewal
每兩天
Post-thaw recovery
快速操作。讓細胞有 24 小時的時間從冷凍過程中恢復。接著計數細胞,若活細胞數超過 10⁶ 個,則進行稀釋。
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
DBA/2