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REH
Tissue
外周血
Disease
急性淋巴細胞白血病(ALL)
Synonyms
Reh

Documents

REH

Cell line · Product number 300320

REH is a human B-cell precursor acute lymphoblastic leukemia (ALL) cell line derived in 1973 from the peripheral blood of a 15-year-old patient during rel...

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1

01General information

Description

REH 是一種人類 B 細胞前體急性淋巴細胞白血病(ALL)細胞系,於 1973 年從一名 15 歲復發期患者的外周血中分離得到。 作為最早建立的 B 細胞前體 ALL 模型之一,它呈現典型的淋巴母細胞形態,並能在懸浮培養中生長,反映了白血病原始細胞的行為特徵。

REH 細胞廣泛用於研究 B-ALL 的生物學特性,包括增殖、存活途徑及治療反應。它們既可支援體外藥物篩選研究,亦可透過免疫缺陷小鼠的異種移植實驗進行體內白血病建模,使其成為研究新型治療策略之臨床前研究的多功能工具。

Tissue
外周血
Disease
急性淋巴細胞白血病(ALL)
Synonyms
  • Reh

02Classification

Organism
Human
Sex
Female
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
圓形細胞
Cell type
淋巴母細胞

04Identifiers

Citation
REH(Cytion 型號 300320)
NCBI TaxID
9606
Cellosaurus
CVCL_1650

05Expression and susceptibility

Antigen expression
CD3 A (17%) B (17%) C (20%)、CD4 (15%)、CD10 (55%)、CD20+、HLA-DR+、CALLA+

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% 經熱滅活的胎牛血清
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。
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
15年
Ethnicity
高加索人