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Mv-4-11 人急性單核細(xì)胞

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更新時(shí)間:2025-02-12 08:26:51瀏覽次數(shù):36次

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產(chǎn)品名稱:Mv-4-11人急性單核細(xì)胞白血病細(xì)胞、Mv-4-11人急性單核細(xì)胞白血病細(xì)胞、Mv-4-11人急性單核細(xì)胞白血病細(xì)胞、Mv-4-11人急性單核細(xì)胞白血病細(xì)胞

產(chǎn)品名稱:Mv-4-11 人急性單核細(xì)胞白血病細(xì)胞、Mv-4-11 人急性單核細(xì)胞白血病細(xì)胞、Mv-4-11 人急性單核細(xì)胞白血病細(xì)胞、Mv-4-11 人急性單核細(xì)胞白血病細(xì)胞;

人慢性骨髓單核細(xì)胞性白血病MV-4-11

種屬

別稱

MV-4-11; MV-4:11; MV4:11; MV 4;11; MV4;11; MV411; MV(4;11); MV4II

組織來(lái)源

外周血

疾病

單核細(xì)胞白血病

傳代比例/細(xì)胞消化

1:2-1:3傳代

培養(yǎng)基配置

IMDM 培養(yǎng)基;10%胎牛血清; 1%雙抗

簡(jiǎn)介

該細(xì)胞系由Rovera課題組建立 ,來(lái)源于一名患有人雙表型髓性單核細(xì)胞白血病(biphenotypic B myelomonocytic leukemia )的10歲男孩的外周血。

形態(tài)

淋巴母細(xì)胞樣

生長(zhǎng)特征

懸浮生長(zhǎng)

倍增時(shí)間

~48h

基因表達(dá)

CD4( 40-96% CD10( 4-11% CD15( 96-99%)

STR

Amelogenin: X,Y;CSF1PO: 10,12;D13S317: 13;D16S539: 11,12;D5S818: 11,12;D7S820: 8,9;

THO1: 8,9.3;TPOX: 8,11;vWA: 14,15

培養(yǎng)條件

氣相 :空氣 ,95% ;二氧化碳 ,5%。 溫度 :37攝氏度 ,培養(yǎng)箱濕度為70%-80%。

凍存條件

凍存液 :90%FBS ,DMSO 10%,

或使用非程序凍存液 :貨號(hào)JY-H040

保藏機(jī)構(gòu)

ATCC; CRL-9591

備注

該細(xì)胞為懸浮細(xì)胞 ,請(qǐng)注意離心收集細(xì)胞懸液 ,請(qǐng)勿直接倒掉細(xì)胞培養(yǎng)液。

產(chǎn)品使用

于科學(xué)研究 ,不可作為動(dòng)物或人類疾病的治療產(chǎn)品使用。

Peanut allergy affects about 1%-3% of the pediatric population in the world, with an important increase in the last decades. Nowadays, international guidelines recommend the early introduction of peanuts in the infant diet, with poor information about the quantity and the frequency of the intake. Allergen immunotherapy may represent the only therapeutic strategy able to modify the natural history of peanut allergy. In particular, oral immunotherapy showed the most promising results in terms of efficacy, but with significant rates of adverse reactions, mostly gastrointestinal. In 2020, the Food and Drug Administration and the European Medicines Agency approved Palforzia®, an oral drug for patients aged 4-17?years. Several studies are ongoing to improve the tolerability of oral immunotherapy and standardize the desensitization protocols. Sublingual immunotherapy permits to offer much lower doses than oral immunotherapy, but fewer adverse events are shown. Subcutaneous immunotherapy is associated with the greatest systemic adverse effects. Epicutaneous immunotherapy, for which Viaskin® patch was approved, has the highest safety profile. Innovative studies are evaluating the use of biological drugs, such as omalizumab or dupilumab, and probiotics, such as Lactobacillus rhamnosus, in monotherapy or associated with oral immunotherapy. Therapy for peanut allergy is constantly evolving, and new perspectives are ongoing to develop.

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