返回顶部显示 11 - 20 件，共 108 件产品CAT.#SizePriceAnti-Human GST A1-1 Rabbit PolyclonalGS620.1 mL$380.00Anti-human GST K1-1, Mouse Monoclonal AntibodyGS250.1 mg$380.00Anti-Human GST M1-1GS670.1 mL$380.00Anti -人 GST M1-1，小鼠单克隆抗体 GS170.1 mg$380.00抗人 GST M3-3，小鼠单克隆抗体 GS190.1 mg$380.00抗人 GST P1-1GS720.1 mL$380.00抗人 GST T1-1，小鼠单克隆抗体抗体GS200.1 mg$380.00Anti-Rabbit CYP450 1A1/1A2PR311.0 mL$190.00Anti-Rabbit CYP450 2B4PR301.0 mL$280.00Anti-Rabbit Cytochrome b5PR910.1 mL$275.00PaginationFirst page« FirstPrevious page‹ PreviousPage 1当前页2页3页4页5页6页7页8页9…下一页下一页›最后一页最后»返回顶部显示 1 - 10 件，共 108 件产品CAT.#SizePrice(±) 4\'-Hydroxymephenytoin X215 mg$225.00Anti Human GST A1-1 Goat Polyclonal AntibodyGS68100 uL$380.00Anti Rabbit CYP450 2E1PR320.1 mL$280.00Anti Rabbit Epoxide水解酶山羊多克隆抗体PR350.1 mL$280.00Anti-Human CYP450 1A2, Goat PolyclonalPH170.5 mL$425.00Anti-Human CYP450 1A2, Rabbit PolyclonalPA170.1 mL$315.00Anti-Human CYP450 2C10, Rabbit PolyclonalPA220.1 mg$315.00Anti-Human C YP450 2D6，山羊多克隆 PA450.1 mL$310.00 Anti-Human CYP450 2E1, Rabbit Polyclonal PA260.1 mL$315.00Anti-Human CYP450 3A4, Rabbit Polyclonal PA320.1 mL$315.00分页当前页1页2页3页4页5页6页7页8页9…下一页下一页›末页末页»返回页首抗人 CYP450 3A4，兔多克隆抗体$315.00SKUPA32产品概述

CYP450 3A4 抗体是在兔体内针对重组人 P450 3A4 制备的，用于在蛋白质印迹上表征细胞色素 P450。每个小瓶包含的抗体足以进行至少 10 次印迹。

产品文档规格表 PA32 规格相关产品ProductCAT.#SizePriceCypExpress 1A1, 250 mgCE1A1.250250 mg$225.00CypExpress 19A1, 1 GramCE19A1.1g1.0 Gram$465.00GSH/GSSG 检测：CuvetteGT 35套件$385.00CUPRACFood and Beverage Antioxidant AssayFS021 Kit$395.00CypExpress 19A1, 10 克CE19A1.1010.0 克$3,760.00返回页首抗人 CYP450 2E1，兔多克隆抗体$315.00SKUPA26产品概述

该抗体是在兔体内针对重组人 P450 2E1 制备的，旨在用于在蛋白质印迹上表征细胞色素 P450。每个小瓶包含的抗体足以进行至少 10 次印迹。交叉与大鼠反应。

产品文档份量pa26指定的产品生产量。 5.00 cypexpress 1A1, 10.0 克CE1A1.1010.0 克$3,760.00CypExpress 2D6, 1.0 克CE2D6.11.0 克$500.00返回页首抗人 CYP450 2D6，山羊多克隆抗体 $310.00SKUPA45 产品概述

该抗体是在山羊体内针对重组人 P450 2D6 制备的，用于在蛋白质印迹上表征细胞色素 P450。每瓶含有足够进行至少 10 次印迹的抗体。

相关产品ProductCAT.#SizePriceCypExpress 19A1, 250 mgCE19A1.250mg250 mg$210.00活性大鼠尿激酶，HMWVA570.05 mg$390.00CypExpress 2D6, 1.0 GramCE2D6.11.0 Gram$5 00.00GSH/GSSG 含量: CuvetteGT35Kit$385.00CypExpress 19A1, 1 GramCE19A1.1g1.0 Gram$465.00返回顶部抗人 CYP450 2C10，兔多克隆抗体$315.00SKUPA22产品概述

该抗体是针对重组人 CYP450 2C10 制备的，用于在蛋白质印迹上表征 CYP450 2C9 和 2C10。

产品文档规格表 PA22 规格表相关ProductsProductCAT.#SizePriceGSH/GSSG Assay: CuvetteGT35Kit$385.00Human PAI-1（糖基化-潜伏形式）PL770.5 mg$1,145.00GST A1-1，重组人GS600.1 mg$460.00CypExpress 2D6, 1.0 GramCE2D6.11.0 Gram$ 500.00 活性大鼠尿激酶，HMWVA570 .05 毫克 390.00 美元返回顶部抗人 CYP450 1A2，兔多克隆抗体$315.00SKUPA17产品概述

该抗体是针对重组人 CYP450 1A2 制备的，旨在用于在蛋白质印迹上表征 CYP450 1A2。

产品文档规格表 PA17.080328.pdf相关产品ProductCAT.#SizePriceHuman PAI-1（糖基化-活性形式）PL760.5 mg$1,100.00CypExpress 1A1, 250 mgCE1A1.250250 mg$225.00活性大鼠尿激酶，HMWVA570.05 mg$390.00GST A1-1，重组人GS600.1 mg 460.00 美元 GSH/GSSG化验：CuvetteGT35Kit$385.00返回顶部抗人 CYP450 1A2，山羊多克隆抗体 $425.00SKUPH17产品概述

针对纯化的重组人 P450 1A2 制备的山羊 IgG，旨在使用重组酶或完整的人微粒体制剂进行 P450 1A1/1A2 功能的抑制研究。使用重组 P450 1A2 可实现非常高的抑制。在微粒体制剂中观察到的 P450 1A2 抑制水平取决于给定底物对 P450 1A2 代谢的特异性，以及可能代谢测试底物的其他酶的相对水平。也适用于蛋白质印迹。

产品文档规格表 PH17 规格相关产品产品目录.#SizePriceCUPRACFood and Beverage Antioxidant AssayFS021 Kit$395.00CypExpress 19A1, 10 GramsCE19A1.1010.0 Grams$3,760.00CypExpress 1A1, 10.0 GramsCE1A1.10 10.0 克 3,760.00 美元活性大鼠尿激酶，HMWVA570.05 mg$390.00人 PAI-1（糖基化-潜伏形式）PL770.5 mg$1,145.00返回页首抗兔环氧化物水解酶，山羊多克隆抗体$280.00SKUPR35产品概述背景

环氧化物水解酶参与多种药物和其他外源性物质的代谢。这些酶催化水加成环氧化物形成邻位二氢二醇。这通常配置为反式。酶促水合作用基本上是不可逆的，并会产生较低反应性的代谢物，这些代谢物可以很容易地结合和排出体外。许多化合物可诱导微粒体环氧化物水解酶，包括苯巴比妥、反式二苯乙烯氧化物和黄曲霉毒素。

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该抗体是针对纯化的兔环氧化物水解酶制备的，用于通过蛋白质印迹法表征环氧化物水解酶。它还与大鼠环氧化物水解酶发生交叉反应。

产品文档规格表 PR35.pdf相关产品ProductCAT.#SizePriceCypExpress 1A1, 1.0 GramCE1A1.11.0 Gram$500.00GST A1-1, Recombinant HumanGS600.1 mg$460.00Human PAI-1(Glycosylated - Latent Form)PL770.5 mg$1,145.00CypExpress 1A1, 10.0 GramsCE1A1.1010.0 Grams$3,760.00GSH/GSSG Assay: CuvetteGT35Kit$385.00返回顶部抗兔 CYP450 2E1$280.00SKUPR32产品概述

这种针对兔 CYP450 2E1 制备的多克隆山羊 IgG 可用于通过免疫测定或蛋白质印迹法鉴定这种乙醇和吡啶诱导型 P450 形式。

产品文档规格表 PR32.pdf相关产品ProductCAT .#SizePriceCypExpress 19A1, 10 克CE19A1.1010.0 克$3,760.00CypExpress 19A1, 250 毫克CE19A1.250mg250 毫克$210.00GSH/GSSGGT40 试剂盒的微孔板检测$425.00异前列烷EIA 试剂盒EA84K it$350.00人 PAI-1（糖基化-活性形式）PL760.5 mg$1,100.00 This protocol comprises various methods to coculture organoids (particularly human small intestinal and colon organoids) with microbes, including microinjection into the lumen and periphery of 3D organoids and exposure of organoids to microbes in a 2D layer. This protocol outlines the experimental and computational steps of MetaRibo-Seq, a modified ribosome profiling approach that allows direct interrogation of translation in uncultured bacterial communities. This protocol describes a complete workflow for detecting significant contacts in Capture Hi-C data, including preprocessing, interaction calling and downstream analyses, based on the CHiCAGO pipeline and companion tools. Large-scale preparation of fluorescence multiplex host cell reactivation (FM-HCR) reporters The authors provide a protocol for fluorescence multiplex host cell reactivation, which uses reporter plasmids containing site-specific DNA lesions to assess DNA repair capacity in at least six major DNA repair pathways in live cells. Translation of 11C-labeled tracer synthesis to a CGMP environment as exemplified by [11C]ER176 for PET imaging of human TSPO Radiotracers used in human positron emission tomography studies need to be prepared according to current good manufacturing practice. Here we use the synthesis of [11C]ER176 as an example to show the translation of an experimental radiosynthesis to a current good manufacturing practice process. Identification of cancer-related mutations in human pluripotent stem cells using RNA-seq analysis Human pluripotent stem cells acquire cancer-related mutations during culture, which can impact their use in the clinic or in basic research. This protocol describes a computational pipeline to detect such mutations using RNA sequencing data. Genome-wide and sister chromatid-resolved profiling of protein occupancy in replicated chromatin with ChOR-seq and SCAR-seq The authors describe procedures for genome-wide quantification of histone modifications and chromatin-associated proteins after replication (chromatin occupancy after replication-seq) and for profiling their relative occupancy in nascent sister chromatids (sister chromatids after replication-seq). Interrogating in vivo T-cell metabolism in mice using stable isotope labeling metabolomics and rapid cell sorting This protocol describes how to rapidly isolate a specific cell type from mouse blood or tissues for mass-spectrometry-based metabolomics. Mice are infused with isotopically labeled compounds, and cells are isolated using antibody-coated magnetic beads. Millman and colleagues describe a six-stage monolayer culture differentiation protocol for generating insulin-secreting pancreatic 尾 cells from a variety of human pluripotent stem cell lines and outline steps for in vitro functional assessment. SorTn-seq: a high-throughput functional genomics approach to discovering regulators of bacterial gene expression This protocol describes a high-throughput sequencing approach to identifying regulators of bacterial gene expression based on transposon insertion mutagenesis in a strain harboring a fluorescent reporter. NovoSpaRc: flexible spatial reconstruction of single-cell gene expression with optimal transport This protocol describes novoSpaRc, a computational pipeline for de novo reconstruction of spatial gene expression from single-cell RNA sequencing with the potential to incorporate spatial atlas data to improve the reconstruction. Rapid ex vivo molecular fingerprinting of biofluids using laser-assisted rapid evaporative ionization mass spectrometry This high-throughput protocol for direct ex vivo real-time metabolic fingerprinting of biofluids uses a laser system and an automated sampling platform. It includes REIMS procedures for analyzing blood, urine, stool, saliva, sputum and breast milk. This protocol describes how to use free-space angular-chirp-enhanced delay (FACED), an all-optical, passive and reconfigurable laser-scanning approach, to increase the imaging speed of various microscopy modalities. FLEP-seq: simultaneous detection of RNA polymerase II position, splicing status, polyadenylation site and poly(A) tail length at genome-wide scale by single-molecule nascent RNA sequencing This protocol describes isolation and long-read sequencing (using either the Oxford Nanopore or PacBio platforms) of nascent chromatin-associated RNAs from Arabidopsis seedlings and bioinformatic pipelines for profiling splicing and polyadenylation. Regional and functional division of functional elements of solid-state nanochannels for enhanced sensitivity and specificity of biosensing in complex matrices This protocol enables explicit regional and functional division of functional elements of solid-state nanochannels to improve the sensitivity and specificity of bioanalysis in complex matrices. Metabolomics studies using large-scale NMR or mass spectrometry experiments on biofluids or tissues generate complex data. This protocol provides guidelines and software (supplied in Jupyter notebooks) for the statistical analysis of these data. The glomerulus is a difficult-to-isolate structure that is often poorly represented in single-cell kidney preparations. This protocol describes the isolation of high-quality mouse glomerular cells for high-throughput analyses. A plate-based single-cell ATAC-seq workflow for fast and robust profiling of chromatin accessibility This protocol describes a plate-based ATAC-seq assay that combines up-front bulk tagging of accessible DNA by the Tn5 transposase with FACS sorting for robust and cost-efficient profiling of chromatin accessibility in single cells. This is a protocol for profiling the methylome and transcriptome of a single cell by using Smart-seq2 and reduced representation bisulfite sequencing. This protocol provides step-by-step instructions for using MetaNeighbor, a computational tool that allows quantification of cell-type replicability across single-cell transcriptomic datasets and identifies the gene sets that contribute to cell identity.