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首頁(yè) ? D2.0R雌性BALB/c小鼠D2乳腺增生性肺泡結(jié)節(jié)腫瘤細(xì)胞株mouse) breast cancer cell liine BioVector NTCC?典型培養(yǎng)物保藏中心

D2.0R雌性BALB/c小鼠D2乳腺增生性肺泡結(jié)節(jié)腫瘤細(xì)胞株mouse) breast cancer cell liine BioVector NTCC?典型培養(yǎng)物保藏中心

  • 價(jià)  格:¥99865
  • 貨  號(hào):NTCC?-D2.0
  • 產(chǎn)  地:北京
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NTCC? D2.0R細(xì)胞系(或稱 D2OR,Cellosaurus登錄號(hào)CVCL_0I88)是一種鼠源(小鼠)乳腺癌細(xì)胞模型,在癌癥研究中被廣泛用于研究腫瘤休眠和轉(zhuǎn)移復(fù)發(fā)。它通常與相關(guān)的、高增殖性的D2A1細(xì)胞系進(jìn)行比較研究。

主要特性與研究?jī)r(jià)值
  • 起源: D2.0R細(xì)胞源自雌性BALB/c小鼠的D2乳腺增生性肺泡結(jié)節(jié)腫瘤,但其建系來(lái)源的腫瘤不易形成自發(fā)性轉(zhuǎn)移。

  • 表型: 它的特點(diǎn)是在特定的微環(huán)境(體內(nèi)和體外)中表現(xiàn)出休眠或靜止表型。這些細(xì)胞可以以單個(gè)非增殖細(xì)胞的狀態(tài)長(zhǎng)期存活,然后在特定條件下重新激活并形成轉(zhuǎn)移灶。

  • TGF- β –mediated EMT decreases mammary branching of D2.OR cells. (A)... |  Download Scientific Diagram


  • 研究用途: 該細(xì)胞系對(duì)于研究控制腫瘤從休眠狀態(tài)轉(zhuǎn)變?yōu)榍忠u性、增殖性轉(zhuǎn)移生長(zhǎng)的機(jī)制至關(guān)重要。研究人員利用它來(lái)探討細(xì)胞外基質(zhì)(ECM)成分(如I型膠原蛋白可誘導(dǎo)增殖)和免疫系統(tǒng)(如自然殺傷細(xì)胞在維持休眠中起關(guān)鍵作用)在調(diào)節(jié)休眠中的作用。

  • 休眠標(biāo)志物: 休眠的D2.0R細(xì)胞通常表達(dá)較低水平的增殖標(biāo)志物Ki-67、磷酸化ERK,而表達(dá)較高水平的p38以及休眠相關(guān)基因,如Cfh和Gas6。ERK/p38活性的比例被認(rèn)為是判斷細(xì)胞增殖或休眠狀態(tài)的關(guān)鍵指標(biāo)。

  • 培養(yǎng)條件: 在使用基底膜提取物(BME)基質(zhì)的標(biāo)準(zhǔn)3D培養(yǎng)系統(tǒng)中,D2.0R細(xì)胞通常保持靜止(休眠)狀態(tài),而D2A1細(xì)胞則會(huì)增殖。

D2.0R模型已證實(shí),使用針對(duì)活躍增殖細(xì)胞的常規(guī)化療可能會(huì)“放過(guò)”非分裂的休眠癌細(xì)胞,而這些細(xì)胞正是后期轉(zhuǎn)移的根源。這強(qiáng)調(diào)了開(kāi)發(fā)專門針對(duì)休眠細(xì)胞的治療方法的重要性。自體吞噬(Autophagy,又稱細(xì)胞自噬)被發(fā)現(xiàn)是促進(jìn)休眠D2.0R細(xì)胞存活的關(guān)鍵機(jī)制之一。

The D2.0R cell line (also written as D2.0R or D2OR, Cellosaurus accession CVCL_0I88) is a murine (mouse) breast cancer cell line widely used in cancer research as a model for studying tumor dormancy and metastatic relapse. It is typically compared with the related, highly proliferative D2A1 cell line.
Key Characteristics
  • Origin: The D2.0R cells were derived from a D2 hyperplastic alveolar nodule mammary tumor in a female BALB/c mouse, but were established from a tumor that did not readily form spontaneous metastases.

  • Phenotype: They are characterized by a dormant or quiescent phenotype in certain microenvironments both in vivo and in vitro, meaning they can survive as solitary, non-proliferating cells for extended periods before potentially forming metastases.

  • Breast cancer dormancy is associated with a 4NG1 state and not senescence |  npj Breast Cancer

  • Research Use: This cell line is crucial for investigating the mechanisms that control the switch from a dormant state to aggressive, proliferative metastatic growth. Researchers use it to study the role of the extracellular matrix (ECM) composition (e.g., type I collagen induces proliferation) and the immune system (e.g., natural killer cells are key for maintaining dormancy) in regulating dormancy.

  • Dormancy Markers: Dormant D2.0R cells express specific markers such as low levels of the proliferation marker Ki-67, low levels of phosphorylated ERK, high levels of p38, and high levels of dormancy-related genes like Cfh and Gas6.

  • Culture Conditions: In a standard 3D culture system using a basement membrane extract (BME) matrix, D2.0R cells typically remain quiescent (dormant), while the D2A1 cells proliferate.

The D2.0R model has been instrumental in demonstrating that effectively targeting proliferating cells with chemotherapy may spare non-dividing cancer cells, which can give rise to late-developing metastases. This highlights the need for therapies that specifically target dormant cells.


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