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Cellcraft  |  SKU: CELL-POR-FIB-HDR

Cellcraft Spontaneously Immortalised Porcine Preadipocyte Cells

原价 £20,000.00

(加上运费 - 在结账时计算)

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可用性

有库存。直接从Cellcraft发货到研究和生产设施,全球配送。

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支持

Cellcraft 提供直接的售后支持,包括故障排除、流程优化和协议指导。可根据要求提供批次特定的文件。

支付

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支持的支付方式

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法律

大多数产品不需要额外的协议。细胞系和某些生物材料在首次从每个供应商购买时需要材料转移协议 (MTA)。我们以数字方式处理 - 双方在发货前在线签署。来自同一供应商的后续订单将立即进行处理。

A spontaneously immortalized porcine preadipocyte cell line isolated from the subcutaneous fat of Sus scrofa via enzymatic tissue digestion. These cells represent an immature precursor lineage committed to adipocyte development, naturally residing in adipose tissue where they maintain the capacity to proliferate and differentiate into mature, lipid-accumulating fat cells upon receiving specific hormonal signals.

The line was established through prolonged in vitro culture, achieving immortalization spontaneously after surpassing the Hayflick limit and successfully navigating a subsequent crisis phase. This process resulted in a stable proliferative capacity and continuous growth performance without the need for exogenous immortalizing agents or genetic modifications. Growth kinetics captured over 40 passages (~140 doublings) demonstrate a robust and consistent average doubling time of 21 hours.

Cells are supplied in a 1.8 mL cryovial at a density of 1 × 10⁶ cells/mL (Lot rWCB01) and must be stored in the vapor phase of liquid nitrogen. The cell line is confirmed negative for Mycoplasma and common pathogens, with a guaranteed post-thaw viability of >70%. Phenotypic characterization via flow cytometry confirms the line is >90% positive for CD90 and contains a ~25% subpopulation of FAP (fibroblast activated protein) positive cells, while remaining negative (<5%) for CD34, CD45, and CD31.

Comprehensive documentation is provided, including brightfield phase microscopy imagery and fluorescent labeling data of neutral lipids following 10 days in adipogenic medium to confirm differentiation potential. The recommended culture environment utilizes DMEM/F12 supplemented with 10% FBS and 10ng/mL FGF2 to maintain optimal adherent growth.

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