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- 保存条件:
常温
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根据瓶身LOT号查询
- 英文名:
4-Imidazoleacrylic acid
- 库存:
有现货
- 供应商:
浙江羽翔生物科技有限公司
- CAS号:
104-98-3
- 规格:
5G
属性
生物来源
synthetic
方案
99%
表单
powder
mp
226-228 °C (lit.)
官能团
carboxylic acid
SMILES字符串
OC(=O)\C=C\c1c[nH]cn1
InChI
1S/C6H6N2O2/c9-6(10)2-1-5-3-7-4-8-5/h1-4H,(H,7,8)(H,9,10)/b2-1+
InChI key
LOIYMIARKYCTBW-OWOJBTEDSA-N
一般描述
应用
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文献和实验ChIP-seq analysis of the LuxR-type regulator VjbR reveals novel insights into the Brucella virulence gene expression network.
LuxR-type transcription factors control diverse physiological functions necessary for bacterial adaptation to environmental changes. In the intracellular pathogen Brucella, the LuxR homolog VjbR has been shown to regulate the expression of virulence factors acting at early stages of the intracellular infection and, directly or indirectly, hundreds of additional genes. However, the precise determination of VjbR direct targets has so far proved elusive. Here, we performed chromatin immunoprecipitation of VjbR followed by next-generation sequencing (ChIP-seq). We detected a large amount of VjbR-binding sites distributed across the Brucella genome and determined a markedly asymmetric binding consensus motif, an unusual feature among LuxR-type regulators. RNA-seq analysis performed under conditions mimicking the eukaryotic intracellular environment revealed that, among all loci associated to VjbR-binding, this regulator directly modulated the expression of only a subset of genes encoding functions consistent with an intracellular adaptation strategy for survival during the initial stages of the host cell infection. Other VjbR-binding events, however, showed to be dissociated from transcription and may require different environmental signals to produce a transcriptional output. Taken together, our results bring new insights into the extent and functionality of LuxR-type-related transcriptional networks.
双苯咪唑类的Hochest-33342和33258及 JC-1染色
双苯咪唑类的Hochest-33342和33258及 JC-1染色 双苯咪唑类的Hochest-33342和33258 该染料可渗透细胞 膜进入细胞内,与DNA结合,使之染色。凋亡细胞对该染料的摄取增高,染色后呈强蓝色荧光。其实验方法如下。 (1)细胞培养及凋亡的诱导:将细胞接种在10cm的培养皿中(106 细胞),在适当的时机诱导细胞凋亡。 (2)收集细胞:悬浮生长的细胞
4) 0.87 gSodium phosphate monobasic (Na2HPO4* H2O) 0.54 gSodium chloride 8.5 gHPLC water 1.00 LAdgust PH to 7.4 with 1N NaOH 1M HClSLGMA Immunp Chemical SIGMA DiagnosticsAnti-mouse IgG (Fab specific) Sigma 104 PhosphataseAlaline Phosphatase conjugate
相关专题 蛋白表达技术全攻略 本指南介绍了大规模和小规模GST蛋白表达 和纯化的方法。由于蛋白的多样性,因此推荐先进小规模表达及纯化测试。 材料与试剂 1. IPTG (Sigma) 2. 咪唑 (Sigma) 3. 蛋白酶抑制剂 (Roche) 4. 溶菌酶(Sigma) 5. 谷胱甘肽 琼脂 糖 4B 珠 (Pierce 15160) 6. 谷胱
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