杭州仟諾生物科技有限公司17504-044B-27® 添加劑是無(wú)血清添加劑 N2等常用試劑大量現(xiàn)貨備貨，到貨

B-27® 添加劑是無(wú)血清添加劑，用于海馬神經(jīng)元和其他中樞神經(jīng)系統(tǒng)（CNS）神經(jīng)元的生長(zhǎng)和保持其短期或長(zhǎng)期活性。B-27® 添加劑是50X 的液體，可以與Neurobasal® 培養(yǎng)基或Neurobasal®-A 培養(yǎng)基組合使用，用于神經(jīng)細(xì)胞培養(yǎng)而不需要再添加飼養(yǎng)層細(xì)胞。

B-27® 添加劑適和應(yīng)用于大多數(shù)神經(jīng)細(xì)胞培養(yǎng)。對(duì)于特別的應(yīng)用，我們提供 其他配方的B-27® 添加劑.

質(zhì)量控制檢測(cè) 
B-27® 添加劑 進(jìn)行了18天妊娠的原代大鼠（Sprague Dawley） 的胚胎海馬神經(jīng)元生長(zhǎng)檢測(cè)。 通過(guò)了細(xì)菌和真菌的檢測(cè). B-27® 也做了1X 濃度的內(nèi)毒素水平測(cè)試。 

僅供研究使用。除非另有說(shuō)明，不得用于任何動(dòng)物或人類(lèi)治療或診斷。

詳細(xì)說(shuō)明

B-27® 添加劑是無(wú)血清添加劑

常用規(guī)格

引文和參考文獻(xiàn) （17）

• D2 receptors inhibit the secretory process downstream from calcium influx in dopaminergic neurons: implication of K+ channels.

作者

Congar P; Bergevin A; Trudeau LE

雜志

J Neurophysiol （2002） 87:1046-1102

產(chǎn)品用途

Using a culture system in which isolated DAergic neurons establish self-innervating synapses （"autapses"） that release both DA and glutamate, we studied the mechanism by which presynaptic D2 receptors inhibit glutamate-mediated excitatory postsynaptic currents （EPSCs）.

ID:

PN64425

• Decreased synaptic vesicle recycling efficiency and cognitive deficits in amphiphysin 1 knockout mice.

作者

Di Paolo Gilbert; Sankaranarayanan Sethuraman; Wenk Markus R; Daniell Laurie; Perucco Ezio; Caldarone Barbara J; Flavell Richard; Picciotto Marina R; Ryan Timothy A; Cremona Ottavio; De Camilli Pietro;

雜志

Neuron （2002） 33:789-804

產(chǎn)品用途

Primary cultures of cortical neurons were prepared. Cells were maintained up to 3 weeks in Neurobasal/B27 medium at 37°C in a 5% CO2 humidified incubator.

ID:

PN47418

• Blocking HES1 expression initiates GABAergic differentiation and induces the expression of p21（CIP1/WAF1） in human neural stem cells.

作者

Kabos Peter; Kabosova Andrea; Neuman Toomas;

雜志

J Biol Chem （2002） 277:8763-8769

產(chǎn)品用途

Resected human fetal brain tissue was placed into ice cold DMEM/F-12 with penicillin/streptomycin for further dissection. The tissue was cut into small pieces and trypsinized （0.02 mg/ml trypsin in versene （Invitrogen） at 37 °C for 10 min. Cell suspension was centrifuged at 400 rpm for 5 min, the pellet was washed once with DMEM/F-12 and plated at a density of 5000-10,000 viable cells/ml in the growth medium DMEM/F-12, B27 supplement （Invitrogen）. Cells were washed with PBS （Invitrogen）

ID:

PN63471

• Long-term culture of mouse cortical neurons as a model for neuronal development, aging, and death.

作者

Lesuisse Christian; Martin Lee J;

雜志

J Neurobiol （2002） 51:9-23

產(chǎn)品用途

A long-term cell culture system was used to study maturation, aging, and death of cortical neurons.

ID:

PN60461

• An improved method for the expression of TRH in serum-supplemented primary cultures of fetal hypothalamic cells.

作者

Joseph-Bravo Patricia; Pérez-Martínez Leonor; Lezama Leticia; Morales-Chapa Claudia; Charli Jean Louis;

雜志

Brain Res Brain Res Protoc （2002） 9:93-104

產(chǎn)品用途

Primary cultures of dispersed cells from fetal nervous tissue are extensively used for studying multiple neuronal properties

ID:

PN62028