標(biāo)準(zhǔn)物質(zhì)一站式采購(gòu)平臺(tái)
在生命科學(xué)研究的探索之路上,每一項(xiàng)突破性成果的背后,都離不開(kāi)可靠實(shí)驗(yàn)工具的堅(jiān)實(shí)支撐。近期,多篇發(fā)表于國(guó)際頂尖期刊的高分文獻(xiàn),再次印證了BNCC產(chǎn)品的專業(yè)實(shí)力,這些高分論文覆蓋多個(gè)前沿領(lǐng)域,來(lái)自國(guó)內(nèi)一流科研院校與機(jī)構(gòu)的團(tuán)隊(duì),從細(xì)胞系、微生物菌種到優(yōu)質(zhì)培養(yǎng)基,BNCC全系列產(chǎn)品深度參與實(shí)驗(yàn)流程,為科研數(shù)據(jù)的準(zhǔn)確性保駕護(hù)航。
論文1:《Integrated single-cell and spatial transcriptomics uncover distinct cellular subtypes involved in neural invasion in pancreatic cancer》
內(nèi)容摘要:Nerves are integral to tumor biology, yet the peri- and intra-neural microenvironment and their roles in cancer-neural invasion (NI) remain underexplored. Here, we perform single-cell/single-nucleus RNA sequencing (sc/snRNA-seq) and spatial transcriptomics on 62 samples from 25 pancreatic ductal adenocarcinoma (PDAC) patients, mapping cellular composition, lineage dynamics, and spatial organization across varying NI statuses. Tertiary lymphoid structures are abundant in low-NI tumor tissues and co-localize with non-invaded nerves, while NLRP3+ macrophages and cancer-associated myofibroblasts surround invaded nerves in high-NI tissues. We identify a unique endoneurial NRP2+ fibroblast population and characterize three distinct Schwann cell subsets. TGFBI+ Schwann cells locate at the leading edge of NI, can be induced by transforming growth factor β (TGF-β) signaling, promote tumor cell migration, and correlate with poor survival. We also identify basal-like and neural-reactive malignant subpopulations with distinct morphologies and heightened NI potential. This landscape depicting tumor-associated nerves highlights critical cancer-immune-neural interactions in situ and enlightens treatment development targeting NI.
發(fā)表期刊:CANCER CELL
影響因子:44.5
引用BNCC產(chǎn)品:
| 產(chǎn)品編號(hào) | 中文名稱 | 英文名稱 |
| BNCC352264 | 人胰腺癌細(xì)胞 | PANC-1 |
| BNCC358376 | 人雪旺細(xì)胞 (神經(jīng)纖維瘤病1型) | sNF96.2 |
| BNCC364169 | DMEM-H完全培養(yǎng)基(低碳酸氫鈉)(含10%FBS) | / |
論文2:《Alistipes finegoldii augments the efficacy of immunotherapy against solid tumors》
內(nèi)容摘要:The emergence of immunotherapy has revolutionized cancer therapy. However, immunotherapeutic resistance remains a major obstacle for broader clinical application. Recent studies highlight that gut microbiota enhances immunotherapy by modulating anti-tumor immunity. In our investigation, we identify that Alistipes finegoldii (A. finegoldii) is associated with superior immunotherapy efficacy across multiple cohorts. Subsequent in vitro and in vivo experiments reveal that A. finegoldii enhances CD8+ T cell chemotaxis via the CXCL16-CXCR6 axis, enhancing immunotherapy efficacy. Mechanistically, a lipoprotein derived from A. finegoldii (LIPOAF) activates the nuclear factor kappa B (NF-κB) signaling pathway to augment CXCL16 expression in CCR7+ conventional dendritic cells through binding with the Toll-like receptor 2. Released CXCL16 subsequently facilitates the recruitment of CXCR6+CD8+ T cells into the tumor microenvironment, effectively curbing tumor growth. Our findings suggest a promising strategy for treating solid tumors by combining A. finegoldii with immunotherapy.
發(fā)表期刊:CANCER CELL
影響因子:44.5
引用BNCC產(chǎn)品:
| 產(chǎn)品編號(hào) | 中文名稱 | 拉丁文名稱 |
| BNCC361741 | 大腸桿菌Nissle1917 | Escherichia coli Nissle1917 |
論文3:《A high-frequency artificial nerve based on homogeneously integrated organic electrochemical transistors》
內(nèi)容摘要:Artificial nerves that are capable of sensing, processing and memory functions at bio-realistic frequencies are of potential use in nerve repair and brain–machine interfaces. n-type organic electrochemical transistors are a possible building block for artificial nerves, as their positive-potential-triggered potentiation behaviour can mimic that of biological cells. However, the devices are limited by weak ionic and electronic transport and storage properties, which leads to poor volatile and non-volatile performance and, in particular, a slow response. We describe a high-frequency artificial nerve based on homogeneously integrated organic electrochemical transistors. We fabricate a vertical n-type organic electrochemical transistor with a gradient-intermixed bicontinuous structure that simultaneously enhances the ionic and electronic transport and the ion storage. The transistor exhibits a volatile response of 27 μs, a 100-kHz non-volatile memory frequency and a long state-retention time. Our integrated artificial nerve, which contains vertical n-type and p-type organic electrochemical transistors, offers sensing, processing and memory functions in the high-frequency domain. We also show that the artificial nerve can be integrated into animal models with compromised neural functions and that it can mimic basic conditioned reflex behaviour.
發(fā)表期刊:Nature Electronics
影響因子:40.9
引用BNCC產(chǎn)品:
| 產(chǎn)品編號(hào) | 中文名稱 | 英文名稱 |
| BNCC100235 | 大鼠腎上腺嗜鉻細(xì)胞瘤細(xì)胞(高分化) | PPC-12(高分化) |
論文4:《De novo design of self-assembling peptides with antimicrobial activity guided by deep learning》
內(nèi)容摘要:Bioinspired materials based on self-assembling peptides are promising for tackling various challenges in biomedical engineering. While contemporary data-driven approaches have led to the discovery of self-assembling peptides with various structures and properties, predicting the functionalities of these materials is still challenging. Here we describe the deep learning-guided de novo design of antimicrobial materials based on self-assembling peptides targeting bacterial membranes to address the emerging problem of bacterial drug resistance. Our approach integrates non-natural amino acids for enhanced peptide self-assembly and effectively predicts the functional activity of the self-assembling peptide materials with minimal experimental annotation. The designed self-assembling peptide leader displays excellent in vivo therapeutic efficacy against intestinal bacterial infection in mice. Moreover, it exhibits an enhanced biofilm eradication capability and does not induce acquired drug resistance. Mechanistic studies reveal that the designed peptide can self-assemble on bacterial membranes to form nanofibrous structures for killing multidrug-resistant bacteria. This work thus provides a strategy to discover functional peptide materials by customized design.
發(fā)表期刊:NATURE MATERIALS
影響因子:38.5
引用BNCC產(chǎn)品:
| 產(chǎn)品編號(hào) | 中文名稱 | 拉丁文名稱 |
| BNCC186732 | 腸致病性大腸埃希氏菌 | Escherichia coli EPEC |
| BNCC363037 | 生癌腸桿菌 | Enterobacter cancerogenus, (Urosevic) Dickey and Zumoff |
| BNCC330867 | 表皮葡萄球菌 | Staphylococcus epidermidis (Winslow and Winslow) Evans |
| BNCC254392 | 鮑曼不動(dòng)桿菌 | Acinetobacter baumannii Bouvet and Grimont |
| BNCC102997 | 肺炎克雷伯氏菌 | Klebsiella pneumoniae |
| BNCC360085 | PAO1銅綠假單胞菌(綠色熒光) | PAO1 Pseudomonas aeruginosa |
科研無(wú)捷徑,品質(zhì)筑根基。BNCC產(chǎn)品持續(xù)獲得頂尖期刊與科研團(tuán)隊(duì)的認(rèn)可,既是對(duì)我們技術(shù)實(shí)力的肯定,更是前行的動(dòng)力。未來(lái),我們將繼續(xù)深耕生物研發(fā)領(lǐng)域,提供更全面的科研解決方案,與全球科研人攜手,助力更多創(chuàng)新成果閃耀學(xué)界!
為回饋廣大客戶長(zhǎng)期以來(lái)對(duì)BNCC產(chǎn)品的信任和支持,現(xiàn)推出“BNCC論文獎(jiǎng)勵(lì)活動(dòng)”,期待您的參與!
志賀氏菌屬(Shigella Castellani),是一類革蘭氏陰性兼厭氧腸桿菌,是引起細(xì)菌性痢疾最為常見(jiàn)的病原菌。在自然界中分布較為廣泛,俗稱痢疾桿菌,主要流行于發(fā)展中國(guó)家。一般在每年8到9月為發(fā)病高峰。
了解更多> >動(dòng)物源性食品因其含有豐富的人體必需營(yíng)養(yǎng)物質(zhì),成為人們飲食構(gòu)架中必不可少的組成部分。BNCC積極響應(yīng)市場(chǎng)需求,近期推出了雞源性核酸檢測(cè)試劑盒(熒光PCR法)與動(dòng)物源性核酸標(biāo)準(zhǔn)質(zhì)控樣品,現(xiàn)貨供應(yīng),歡迎選購(gòu)!
了解更多> >北納生物旗下偉業(yè)計(jì)量標(biāo)準(zhǔn)物質(zhì)研究中心仔細(xì)研究新版的《生活飲用水標(biāo)準(zhǔn)檢驗(yàn)方法》標(biāo)準(zhǔn)后,推出下列完全符合使用場(chǎng)景與要求的生活飲用水檢驗(yàn)的標(biāo)準(zhǔn)物質(zhì)?,F(xiàn)貨供應(yīng),歡迎選購(gòu)!
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