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In 
					recent years, evidence has emerged for the existence of many 
					diverse types of RNA, which play roles in a wide range of 
					biological processes in all kingdoms of life. These 
					molecules generally do not, however, act in isolation, and 
					identifying which proteins partner with RNA is a major 
					challenge. Many methods, in vivo and in vitro, have been 
					used to address this question, including combinatorial or 
					high-throughput approaches, such as systematic evolution of 
					ligands, cross-linking and immunoprecipitation and RNA 
					immunoprecipitation combined with deep sequencing. 					
					
However, 
					most of these methods are not trivial to pursue and often 
					require substantial optimization before results can be 
					achieved. Here, we demonstrate a simple technique that 
					allows one to screen proteins for RNA-binding properties in 
					a gel-shift experiment and can be easily implemented in any 
					laboratory. This assay should be a useful first-pass tool 
					for assessing whether a protein has RNA- or DNA-binding 
					properties, prior to committing resources to more complex 
					procedures.
The principle of RNA EMSA as well as DNA EMSA is simple, considerations for performing a successful RNA EMA including the follows:
1)Needs instruments and reagents for RNA EMSA.
2) The knowledge for handling RNAs and proteins.
3) The skills for running a vertical gel electrophoresis.
4) The facility for imaging ECL signals via x-ray films or imagers for imaging ECL or infrared fluorescence.
5) The RNA probe is expensive, 20 fold of what for making a DNA probes.
6) Most probes for RNA EMSA is a single-strand RNA, which is very fragile for degradation.
7) Working environment should keep as RNase-free.
8) Based on the considerations above, we recommend our IRFluo rEMSA kits for RNA EMSA for its fast results (~2 hours) and simple operation (imaging gels immediately after gel electrophoresis).
9) If using 微奥基因's RNA EMSA service, the results would be secured as the scientists in 微奥基因 Biotech have rich experience for RNA EMSA (Linking to technique services).
通用RNA EMSA Kit
| 产品名 | 目录号 | 产品描述 | 产品包装 | 价格 | 
|---|---|---|---|---|
| CoolShift-BIr | SIDET102 | 非放射性生物素/ECL RNA EMSA成套试剂,(不带探针与膜,查看组份与操作说明)。 | 100次 | 2860元 | 
| CoolShift-IRr | SIDET202 | 非放射性近红外荧光 RNA EMSA成套试剂(不带探针,查看组份与操作说明)。 | 100次 | 2860元 | 
RNA EMSA探针定制
									
										
											
			
					
												 
										
										探针类别 
												目录号 
												规格 
												价格 
												探针用途 
											
											 
										
											生物素RNA探针 
											BPSRV11 
											
											200次 
											
											
											IDT RNA合成价+1450元* 
											用于RNA EMSA、Competitive(竞争)与 
											Supershift (超迁移)EMSA、Pulldown 以及结合蛋白的纯化。 
										
											 
										近红荧光RNA探针 
											BPSRV21 
											
											200次 
											
											
											
											IDT RNA合成价+1750元* 
											用于常规EMSA、Competitive(竞争) 
											EMSA、Supershift (超迁移)EMSA,可以快速完成测定。 
										
											 
										80倍竞争RNA探针 
											CPSRV11 
											12次 
											
											IDT RNA合成价+20%** 
											用于Competitive(竞争) 
											EMSA,确定核酸与蛋白结合的特异性。 
										
											 
										80倍突变RNA探针 
											MPSRV21 
											12次 
											
											IDT RNA合成价+20%** 
											用于Competitive(竞争) 
											EMSA,反证确定核酸与蛋白结合的特异性。 
										
											 
									
								注:*美国IDT网站(www.idtdna.com)查询价格,1450元/1750元的费用包括探针设计、生物素标记或荧光标记、纯化、测定,税费与运费。**20%附加费包括探针设计、订货、税费与运费。