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SK-MEL-1
Tissue
皮膚
Disease
黑色素瘤
Metastatic site
胸淋巴管
Synonyms
SK-Mel-1, SK Mel 1, SK-Mel 1, SK-Mel1, SKMEL-1, SkMEL-1, SKMEL1, SK 1

Documents

SK-MEL-1

Cell line · Product number 300424

This cell line was established in 1966 by F. Oettgen and associates using cells from the thoracic duct of a patient. Pigment granules relating both to synthe...

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

01General information

Description
該細胞系由 F. Oettgen 及其同事於 1966 年利用一名患者的胸管細胞建立。其中存在與合成及吞噬作用均有關聯的色素顆粒。 根據本實驗室的定序、Western blot 及 PCR 結果,此細胞系攜帶 BRAF V600E 突變。該細胞為 N-Ras 野生型。
Tissue
皮膚
Disease
黑色素瘤
Metastatic site
胸淋巴管
Synonyms
  • SK-Mel-1
  • SK Mel 1
  • SK-Mel 1
  • SK-Mel1
  • SKMEL-1
  • SkMEL-1
  • SKMEL1
  • SK 1

02Classification

Organism
Human
Sex
Male
Growth properties
Suspension
Biosafety level
1

03Characteristics

Morphology
球形
Tumourigenic
是的,在裸鼠身上會形成色素性惡性黑色素瘤。在經可的松治療的倉鼠的頰囊中也會形成腫瘤。

04Identifiers

Citation
SK-MEL-1(Cytion 型號 300424)
NCBI TaxID
9606
Cellosaurus
CVCL_0068

05Expression and susceptibility

Antigen expression
A型血,Rh陽性。在惡性黑色素瘤患者中,有63%被檢測出針對此血型的抗體;而在其他疾病患者中,則有10%被檢測出此類抗體。
Isoenzymes
PGM3,1,PGM1,1,ES-D,1,AK-1,1,GLO-1,1-2,G6PD,B,
Mutational profile
V600E 型 BRAF 突變是透過 DNA 檢測方法(定序、RT-PCR)及蛋白質檢測方法(Western Blot)進行檢測的。
Products
黑色素

06Handling and culture

Culture medium
RPMI 1640,含 2.1 mM 穩定型谷氨醯胺,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 15% 的熱滅活胎牛血清
Dissociation reagent
Accutase
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
1 至 2 × 10⁵ 個細胞/mL
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.

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