美國(guó)XonaMicrofluidics公司神經(jīng)元突觸軸突培養(yǎng)板現(xiàn)貨供應(yīng)

XONA MICROFLUIDICS提供了多種用于神經(jīng)元細(xì)胞培養(yǎng)的設(shè)備，包括：
SILICONE DEVICES神經(jīng)元突觸軸突連接微流體培養(yǎng)板

美國(guó)Xona Microfluidics LLC公司提供的神經(jīng)元裝置是光學(xué)透明的聚二甲基硅氧烷（PDMS）和生物惰性制造而成。神經(jīng)元裝置由微槽連接的兩個(gè)腔室組成。神經(jīng)元裝置可以使研究者通過(guò)微流體方式隔離細(xì)胞體與軸突。
Xona提供多種硅膠設(shè)備配置。 SND是原始的2隔室。 TCND具有3個(gè)隔室，可提供多種實(shí)驗(yàn)可能性。圓形設(shè)備（RD）與精選的玻璃底皿兼容，使其可用于活細(xì)胞成像。
我們鎖有的硅膠（PDMS）腔室都需要終用戶自由組裝。
XonaChips?是神經(jīng)元培養(yǎng)的新創(chuàng)新！
XonaChips?已預(yù)先組裝和預(yù)先粘合，比我們?cè)嫉挠袡C(jī)硅設(shè)備更易于使用。這些塑料芯片可改善動(dòng)物模型神經(jīng)元的長(zhǎng)期培養(yǎng)。它們對(duì)于培養(yǎng)人干細(xì)胞來(lái)源的神經(jīng)元te別有用，可提供更好的細(xì)胞附著和長(zhǎng)期生長(zhǎng)。
XonaChips?是光學(xué)透明的，非常適合熒光實(shí)時(shí)成像。

目前，Xona正在提供兩室XonaChips?XC系列，具有150、450或900 μm的微槽屏障。每盒（5）XC系列XonaChips?都裝有2 ml XC Pre-Coat?管。
目前，Xona還提供帶有3個(gè)隔室的XonaChips?XC-T系列，該隔室?guī)в校?）個(gè)500 μm的微溝槽屏障，其中有500 um的中央隔室或1000 um的中央隔室。每盒（5）XC-T系列XonaChips?包括2（2）ml XC Pre-Coat?管。
XC Pre-Coat?和XonaPDL?經(jīng)過(guò)化，可與XonaChips?一起使用。
ChipTray?
長(zhǎng)期培養(yǎng)神經(jīng)元過(guò)程中培養(yǎng)基的蒸發(fā)對(duì)細(xì)胞健康有很大影響。在具有較小孔的微流體裝置和芯片中尤其如此。為了克服這些問(wèn)題，Xona開(kāi)發(fā)了一種獲得專利的ChipTray?，可與XonaChips?，我們的有機(jī)硅設(shè)備以及鎖有其他微流體設(shè)備一起使用。除了減少蒸發(fā)之外，ChipTray?還提供了化的外殼，用于使用空氣物鏡進(jìn)行相襯成像。
托盤的尺寸與標(biāo)準(zhǔn)ANSI微孔板支架兼容。托盤的兩端有兩個(gè)水槽，兩個(gè)用于XonaChips?的槽（XC150，XC450，XC900，XC-T-500或XC-T-1000）。安裝在玻璃上的有機(jī)硅設(shè)備或您要使用的任何其他基于幻燈片的微流體設(shè)備也與這些托盤兼容。在每個(gè)插槽中都有一個(gè)切口，可使用倒置顯微鏡提高圖像質(zhì)量。 ChipTrays已準(zhǔn)備好進(jìn)行組織培養(yǎng)。

訂貨號(hào)	簡(jiǎn)述	貨物狀態(tài)
xona chip
XC150	XonaChip 150 um barrier 5PK includes 2 ml tube XC Pre-Coat	現(xiàn)貨促銷
XC450	XonaChip 450 um barrier 5PK includes 2 ml tube XC Pre-Coat	現(xiàn)貨促銷
XC900	XonaChip 900 um barrier 5PK includes 2 ml tube XC Pre-Coat	現(xiàn)貨促銷
XC-T500	XonaChip 500 um central compartment includes (2) 2 ml tubes XC Pre-Coat	現(xiàn)貨促銷
XC-T1000	XonaChip 1000 um central compartment includes (2) 2 ml tubes XC Pre-Coat	現(xiàn)貨促銷
XonaPDL	Optimized poly-d-lysine solution for Xona platforms	現(xiàn)貨促銷
SILICONE DEVICES ROUND (RD)
RD150	Round Device 150 um barrier 5PK	現(xiàn)貨促銷
RD450	Round Device 450 um barrier 5PK	現(xiàn)貨促銷
RD900	Round Device 900 um barrier 5PK	現(xiàn)貨促銷
SILICONE DEVICES 2-COMPARTMENT (SND)
SND150	Standard Neuron Device 150 um barrier 5PK	現(xiàn)貨促銷
SND450	Standard Neuron Device 450 um barrier 5PK	現(xiàn)貨促銷
SND900	Standard Neuron Device 900 um barrier 5PK	現(xiàn)貨促銷
SILICONE DEVICES 3-COMPARTMENT (TCND)
TCND500	Triple Compartment 500 um central compartment 5PK	現(xiàn)貨促銷
TCND1000	Triple Compartment 1000 um central compartment 5PK	現(xiàn)貨促銷
RD75	Round Device 75 um barrier 5PK	現(xiàn)貨促銷
SND75	Standard Neuron Device 75 um barrier 5PK	現(xiàn)貨促銷
uLP	Microfluidic Local Perfusion Device 5PK	現(xiàn)貨促銷
ChipTray? (pack of 6)	Pack of (6)	現(xiàn)貨促銷
ChipTray? (1 each)	Pack of 1	現(xiàn)貨促銷

產(chǎn)品名稱	產(chǎn)品描述
RD150 神經(jīng)元突觸細(xì)胞微灌流系統(tǒng)	圓形設(shè)備（150微米的微槽屏障）尺寸：直徑約21毫米我們的圓形設(shè)備版本的標(biāo)準(zhǔn)150微米微槽屏障具有大約21毫米的直徑，使其與某些35毫米的玻璃兼容許多研究人員在活細(xì)胞成像系統(tǒng)中使用的底盤。玻璃使用的底盤的內(nèi)孔應(yīng)大于或等于21毫米容納設(shè)備。建議至少有22毫米的空間定位設(shè)備。可以使用更大的玻璃底盤，以及如果需要，玻璃蓋玻片。 Round Device (150 um microgroove barrier) Size: ~ 21 mm diameter Our round device version of the standard 150 um microgroove barrier has an approximate diameter of 21 mm, making it compatible with some 35 mm glass bottom dishes that many researchers use in live cell imaging systems. Glass bottom dishes used should have an inner aperture of 21 mm or more to accommodate the device. At least 22 mm is recommended in order to have room to position the device. Larger glass bottom dishes can be used, as well as glass cover slips, if desired.
RD450 神經(jīng)元突觸細(xì)胞微灌流	Round Device (450 um microgroove barrier) Size: ~ 21 mm diameter Our round device version of the standard 450 um microgroove barrier has an approximate diameter of 21 mm, making it compatible with some 35 mm glass bottom dishes that many researchers use in live cell imaging systems. Glass bottom dishes used should have an inner aperture of 21 mm or more to accommodate the device. At least 22 mm is recommended in order to have room to position the device. Larger glass bottom dishes can be used, as well as glass cover slips, if desired.
RD900 神經(jīng)元突觸細(xì)胞微灌流	Round Device (900 um microgroove barrier) Size: ~ 21 mm diameter Our round device version of the standard 900 um microgroove barrier has an approximate diameter of 21 mm, making it compatible with some 35 mm glass bottom dishes that many researchers use in live cell imaging systems. Glass bottom dishes used should have an inner aperture of 21 mm or more to accommodate the device. At least 22 mm is recommended in order to have room to position the device. Larger glass bottom dishes can be used, as well as glass cover slips, if desired.
SND150 神經(jīng)元突觸細(xì)胞微灌流	Standard Neuron Device (150 um microgroove barrier) Size: ~ 22 mm ¨C ~23mm The 150 um neuron device with its shorter microgroove barrier is suitable for researchers who would like to isolate both axons and dendrites. It is also suitable for certain neuronal cultures that do not grow long processes. Researchers who wish to study the early events of axonal and dendritic growth may also find the 150 um device useful. The 150 um device also offers the benefits of fluidic isolation and culture organization for transport studies.
SND450 神經(jīng)元突觸細(xì)胞微灌流	Standard Neuron Device (450 um microgroove barrier) Size: ~ 22 mm ¨C ~23mm The 450 um neuron device is our most popular device. For most applications it is suitable for separating cell bodies from axons. After two weeks, dendrites in E18 rat cortical neurons have typically not crossed the microgroove barrier. The 450 um neuron device also provides the added features of fluidic isolation and culture organization for transport studies.
SND900 神經(jīng)元突觸細(xì)胞微灌流	Standard Neuron Device (900 um microgroove barrier) Size: ~ 22 mm ¨C ~23mm The 900 um neuron device, with its wide microgroove barrier, is suitable for researchers who would like to perform long term experiments while ensuring axonal isolation. In some cultures, after two weeks of growth dendrites may cross the 450 um barrier thereby necessitating the use of the 900 um device.It is also suitable for certain neuronal cultures which grow long processes. Researchers who also wish to make sure they are isolating 100% axons only in the distal chamber may also find the 900 um device useful. The 900 um device also offers the benefits of fluidic isolation and culture organization for transport studies.
TCND500 500um三腔神經(jīng)元設(shè)備	三腔神經(jīng)元設(shè)備（500 um微槽屏障）尺寸：?38毫米-C?24毫米 TCND500由（2）500 um的微溝槽柵欄和500 um的中央柵欄組成室。該設(shè)備使培養(yǎng)皮層神經(jīng)元成為可能。培養(yǎng)海馬神經(jīng)元或其他時(shí)的左右腔室細(xì)胞的組合，在中間。三室也適用于研究人員希望治療軸突中部的運(yùn)輸研究在中間室生長(zhǎng)，同時(shí)觀察生長(zhǎng)錐或在體腔中。神經(jīng)元也可以裝在中央室并對(duì)左右車廂進(jìn)行不同的處理。 Triple Chamber Neuron Device (500 um microgroove barrier) Size: ~ 38 mm ¨C ~24mm The TCND500 consists of (2) 500 um microgroove barriers with a 500 um central chamber. This device makes it possible to culture cortical neurons in the left and right chambers while culturing hippocampal neurons, or other combinations of cells, in the middle. The triple chamber is also suitable for transport studies where the researcher wishes to treat the middle of the axon growing in the middle chamber while observing effects at the growth cone or in the somal compartment. Neurons can also be loaded in the central chamber and different treatments applied to the left and right compartments.
TCND1000 1000um三腔神經(jīng)元設(shè)備	三腔神經(jīng)元設(shè)備（1000 um 微槽屏障）尺寸：尺寸：?38毫米¨C?24mm TCND1000由（2）500 um的微溝槽屏障和1000 um構(gòu)成中央室。該設(shè)備使培養(yǎng)皮層神經(jīng)元成為可能在培養(yǎng)海馬神經(jīng)元或其他細(xì)胞的同時(shí)，左室和右室細(xì)胞的組合，在中間。三室也適用于研究人員希望治療軸突中部的運(yùn)輸研究在中間室生長(zhǎng)，同時(shí)觀察生長(zhǎng)錐或在體腔中。神經(jīng)元也可以裝在中央室并且對(duì)左右車廂進(jìn)行了不同的處理。 Triple Chamber Neuron Device (1000 um microgroove barrier) Size: Size: ~ 38 mm ¨C ~24mm The TCND1000 consists of (2) 500 um microgroove barriers with a 1000 um central chamber. This device makes it possible to culture cortical neurons in the left and right chambers while culturing hippocampal neurons, or other combinations of cells, in the middle. The triple chamber is also suitable for transport studies where the researcher wishes to treat the middle of the axon growing in the middle chamber while observing effects at the growth cone or in the somal compartment. Neurons can also be loaded in the central chamber and different treatments applied to the left and right compartments.
uLP	>微流局部灌流裝置屏障，（50 um microgroove 75微米灌注通道，500 um microgroove 障礙）尺寸：?40毫米-C?24毫米我們的微流體局部灌注腔室shou次發(fā)表在Neuron上。 2010年 4月15日； 66（1）：57-68。該設(shè)備有一個(gè)75微米的灌注室，帶有一套左側(cè)寬度為50 um的微溝槽和一組微溝槽正確的寬度為500 um。此設(shè)備與注射泵或其他合適的設(shè)備，允許研究人員灌注所選的目標(biāo)區(qū)域中的各種療法和化合物。注射泵或其他正確使用所需的合適設(shè)備。欲了解更多信息請(qǐng)見(jiàn)神經(jīng)元。 2010 Apr 15; 66（1）：57-68。 Microfluidic Local Perfusion Device barrier, (50 um microgroove 75 micron perfusion channel, 500 um microgroove barrier) Size: ~ 40 mm ¨C ~24 mm Our Microfluidic Local Perfusion Chamber was first published in Neuron. 2010 Apr 15;66(1):57-68. This device has a 75 micron perfusion chamber with a set of microgrooves on the left 50 um in width and a set of microgrooves on the right 500 um in width. This device, in conjuction with a syringe pump or other suitable equipment, allows the researcher to perfuse selected treatments and compounds across the target area. Syringe pump or other suitable equipment required for proper use. For more indepth information please see Neuron. 2010 Apr 15;66(1):57-68.

2018

Activated Protein C blocks the inhibitory effect on neurite outgrowth by extracellular histones that mediates its inhibition through a retrograde YB-1 signal
July 9, 2018

Exosomes derived from high-glucose-stimulated Schwann cells promote development of diabetic peripheral neuropathy.
FASEB J. 2018 Jun 22:fj201800597R. doi: 10.1096/fj.201800597R. [Epub ahead of print]

Microfluidics of Small-Population Neurons Allows for a Precise Quantification of the Peripheral Axonal Growth State
Front Cell Neurosci. 2018; 12: 166. June 15, 2018

Advances in ex vivo models and lab-on-a-chip devices for neural tissue engineering.
Biomaterials. 2018 May 11. pii: S0142-9612(18)30347-8. doi: 10.1016/j.biomaterials.2018.05.012. [Epub ahead of print]

Neuronal subtype determines HSV-1 Latency-Associated-Transcript (LAT) promoter activity during latency.
J Virol. 2018 Apr 11. pii: JVI.00430-18. doi: 10.1128/JVI.00430-18. [Epub ahead of print]

Axonal Activation of the Unfolded Protein Response Promotes Axonal Regeneration Following Peripheral Nerve Injury.
Neuroscience. 2018 Apr 1;375:34-48. doi: 10.1016/j.neuroscience.2018.02.003. Epub 2018 Feb 10.

Exosomes taken up by neurons hijack the endosomal pathway to spread to interconnected neurons.
Acta Neuropathol Commun. 2018 Feb 15;6(1):10. doi: 10.1186/s40478-018-0514-4.

Neurturin is a PGC-1a1-controlled myokine that promotes motor neuron recruitment and neuromuscular junction formation.
Mol Metab. 2018 Jan;7:12-22. doi: 10.1016/j.molmet.2017.11.001. Epub 2017 Nov 7.

Importin α1 is required for nuclear import of herpes simplex virus proteins and capsid assembly in fibroblasts and neurons.
PLoS Pathog. 2018 Jan 5;14(1):e1006823. doi: 10.1371/journal.ppat.1006823. eCollection 2018 Jan.

Visualization of local phosphatidylcholine synthesis within hippocampal neurons using a compartmentalized culture system and imaging mass spectrometry
Biochem Biophys Res Commun. 2018 Jan 1;495(1):1048-1054. doi: 10.1016/j.bbrc.2017.11.108. Epub 2017 Nov 21.

Intercellular transfer of pathogenic a-synuclein by extracellular vesicles is induced by the lipid peroxidation product 4-hydroxynonenal
Neurobiol Aging. 2018 Jan;61:52-65. doi: 10.1016/j.neurobiolaging.2017.09.016. Epub 2017 Sep 22.

2017

Distal axotomy enhances retrograde presynaptic excitability onto injured pyramidal neurons via trans-synaptic signaling.
Nat Commun. 2017 Sep 20;8(1):625.

Microfluidic Device for Studying Traumatic Brain Injury
Part of the Neuromethods book series (NM, volume 126) First Online: 12 May 2017

Mild and repetitive very mild axonal stretch injury triggers cystoletal mislocalization and growth cone collapse
PLoS One. 2017; 12(5): e0176997. Published online 2017 May 4.

Using high-throughput barcode sequencing to efficiently map connectomes
Nucleic Acids Res. 2017 Jul 7. 45(12): e115. Published online 2017 Apr 26

Messenger RNAs localized to distal projections of human stem cell derived neurons.
Sci Rep 7. 2017 Apr 4;7(1):611. Published online

NGF-dependent axon growth and regeneration are altered in sympathetic neurons of dystrophic mdx mice.
Mol Cell Neurosci. 2017 Feb 2;80:1-17 [Epub ahead of print]

T-type Ca2+ channels are required for enhanced sympathetic axon growth by TNFα reverse signaling Open Biology. Published 18 January 2017.DOI: 10.1098/rsob.160288

The release and trans-synaptic transmission of Tau via exosomes
Mol Neurodegener. 2017; 12: 5. Published online 2017 Jan 13.

MiR-29c/PRKCI Regulates Axonal Growth of Dorsal Root Ganglia Neurons Under Hyperglycemia.
Mol Neurobiol. 2017 Jan 9. [Epub ahead of print]

Co-culture Synaptogenic Assay: A New Look at Fluorescence Reporters and Technological Devices.
Methods Mol Biol. 2017;1538:13-27qua

2016

Acetylated tubulin is essential for touch sensation in mice
eLife. 2016; 5: e20813. Published online 2016 Dec 13

Mesenchymal Stromal Cells Promote Axonal Outgrowth Alone and Synergistically with Astrocytes via tPA
PLoS One. 2016; 11(12): e0168345. Published online 2016 Dec 13.

Compartmentalized Microfluidic Platforms: The Unrivaled Breakthrough of In Vitro Tools for Neurobiological Research.
J Neurosci. 2016 Nov 16;36(46):11573-11584.

Pathological α-synuclein transmission initiated by binding lymphocyte-activation gene 3
Science. 2016 Sep 30; 353(6307): aah3374.

TRiC subunits enhance BDNF axonal transport and rescue striatal atrophy in Huntington’s disease
Proc Natl Acad Sci U S A. 2016 Sep 20; 113(38): E5655–E5664. Published online 2016 Sep 6.

Interneuronal Transfer and Distal Action of Tetanus Toxin and Botulinum Neurotoxins A and D in Central Neurons.
Cell Rep. 2016 Aug 16;16(7):1974-87. doi: 10.1016/j.celrep.2016.06.104. Epub 2016 Aug 4.

Probing extracellular Sonic hedgehog in neurons.
Biol Open. 2016 Aug 15;5(8):1086-92. doi: 10.1242/bio.019422.

Leucine Zipper-bearing Kinase promotes axon growth in mammalian central nervous system neurons
Sci Rep. 2016; 6: 31482. Published online 2016 Aug 11.

miR-145 Regulates Diabetes-Bone Marrow Stromal Cell-Induced Neurorestorative Effects in Diabetes Stroke Rats.
Stem Cells Transl Med. 2016 Jul 26. pii: sctm.2015-0349. [Epub ahead of print]

Semaphorin 3C Released from a Biocompatible Hydrogel Guides and Promotes Axonal Growth of Rodent and Human Dopaminergic Neurons.
Tissue Eng Part A. 2016 Jun;22(11-12):850-61. doi: 10.1089/ten.TEA.2016.0008.

A New Defective Helper RNA to Produce Recombinant Sindbis Virus that Infects Neurons but does not Propagate
Front Neuroanat. 2016; 10: 56. Published online 2016 May 24. doi: 10.3389/fnana.2016.00056

Monitoring mRNA Translation in Neuronal Processes Using Fluorescent Non-Canonical Amino Acid Tagging.
J Histochem Cytochem. 2016 May;64(5):323-33. doi: 10.1369/0022155416641604. Epub 2016 Mar 29.

MicroRNA 146a locally mediates distal axonal growth of dorsal root ganglia neurons under high glucose and sildenafil conditions.
Neuroscience. 2016 Aug 4;329:43-53. doi: 10.1016/j.neuroscience.2016.05.005. Epub 2016 May 7.

Retrograde fibroblast growth factor 22 (FGF22) signaling regulates insulin-like growth factor 2 (IGF2) expression for activity-dependent synapse stabilization in the mammalian brain.
Elife. 2016 Apr 15;5. pii: e12151. doi: 10.7554/eLife.12151.

Exosomes Derived from Mesenchymal Stromal Cells Promote Axonal Growth of Cortical Neurons.
Mol Neurobiol. 2016 Mar 19. [Epub ahead of print]

The RNA-binding protein SFPQ orchestrates an RNA regulon to promote axon viability.
Nat Neurosci. 2016 May;19(5):690-6. doi: 10.1038/nn.4280. Epub 2016 Mar 28.

Quantitative and semi-quantitative measurements of axonal degeneration in tissue and primary neuron cultures
J Neurosci Methods. 2016 Jun 15; 266: 32–41. Published online 2016 Mar 28.

Functional Impact of Corticotropin-Releasing Factor Exposure on Tau Phosphorylation and Axon Transport.
PLoS One. 2016 Jan 20;11(1):e0147250. doi: 10.1371/journal.pone.0147250. eCollection 2016.

Compartmentalized Platforms for Neuro-Pharmacological Research.
Curr Neuropharmacol. 2016;14(1):72-86.

D-4F Decreases White Matter Damage After Stroke in Mice
Stroke. 2016 Jan;47(1):214-20. doi: 10.1161/STROKEAHA.115.011046. Epub 2015 Nov 24.

2015

Dual Role of Herpes Simplex Virus 1 pUS9 in Virus Anterograde Axonal Transport and Final Assembly in Growth Cones in Distal Axons.
J Virol. 2015 Dec 23;90(5):2653-63. doi: 10.1128/JVI.03023-15.

The Basic Domain of Herpes Simplex Virus 1 pUS9 Recruits Kinesin-1 To Facilitate Egress from Neurons.
J Virol. 2015 Dec 9;90(4):2102-11. doi: 10.1128/JVI.03041-15.

Dendrosomatic Sonic Hedgehog Signaling in Hippocampal Neurons Regulates Axon Elongation
J Neurosci. 2015 Dec 9; 35(49): 16126–16141.

MicroRNAs in the axon locally mediate the effects of chondroitin sulfate proteoglycans and cGMP on axonal growth
Dev Neurobiol. 2015 Dec; 75(12): 1402–1419. Published online 2015 Jun 24.

Whole transcriptome profiling reveals the RNA content of motor axons
Nucleic Acids Res. 2016 Feb 29; 44(4): e33. Published online 2015 Oct 12.

Synaptic Contacts Enhance Cell-to-Cell Tau Pathology Propagation. Cell Rep. 2015 May 26;11(8):1176-83

Morphometric assessment of toxicant induced neuronal degeneration in full and restricted contact co-cultures of embryonic cortical rat neurons and astrocytes: using m-Dinitrobezene as a model neurotoxicant. Toxicol In Vitro. 2015 Apr;29(3):564-74.

Coupled local translation and degradation regulate growth cone collapse
Nat Commun. 2015; 6: 6888. Published online 2015 Apr 22.

Control of autophagosome axonal retrograde flux by presynaptic activity unveiled using botulinum neurotoxin type a J Neurosci. 2015 Apr 15;35(15):6179-94

Activation of 5-HT7 receptor stimulates neurite elongation through mTOR, Cdc42 and actin filaments dynamics. Front Behav Neurosci. 2015 Mar 11;9:62.

Identifying the primary site of pathogenesis in amyotrophic lateral sclerosis – vulnerability of lower motor neurons to proximal excitotoxicity
Dis Model Mech. 2015 Mar; 8(3): 215–224.

Recording large extracellular spikes in microchannels along many axonal sites from individual neurons. PLoS One. 2015 Mar 3;10(3):e0118514.

Increased migration of olfactory ensheathing cells secreting the Nogo receptor ectodomain over inhibitory substrates and lesioned spinal cord. Cell Mol Life Sci. 2015 Feb 24.

A ?-secretase inhibitor, but not a ?-secretase modulator, induced defects in BDNF axonal trafficking and signaling: evidence for a role for APP. PLoS One. 2015 Feb 24;10(2):e0118379.

2014

Herpes simplex virus gE/gI extracellular domains promote axonal transport and spread from neurons to epithelial cells. J Virol. 2014 Oct;88(19):11178-86.

PTEN inhibition enhances neurite outgrowth in human embryonic stem cell-derived neuronal progenitor cells. J Comp Neurol. 2014 Aug 15;522(12):2741-55.

A-synuclein immunotherapy blocks uptake and templated propagation of misfolded a-synuclein and neurodegeneration. Cell Rep. 2014 Jun 26;7(6):2054-65.

Regulation of axon growth by the JIP1-AKT axis. Dajas-Bailador F, Bantounas I, Jones EV, Whitmarsh AJ. J Cell Sci. 2014 Jan 1;127(Pt 1):230-9.

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美國(guó)XonaMicrofluidics公司神經(jīng)元突觸軸突培養(yǎng)板 現(xiàn)貨供應(yīng)

美國(guó)XonaMicrofluidics公司神經(jīng)元突觸軸突培養(yǎng)板 現(xiàn)貨供應(yīng)

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美國(guó)XonaMicrofluidics公司神經(jīng)元突觸軸突培養(yǎng)板現(xiàn)貨供應(yīng)

美國(guó)XonaMicrofluidics公司神經(jīng)元突觸軸突培養(yǎng)板現(xiàn)貨供應(yīng)