{{'Search' | translate}}
 

Avanti JXN-30

Avanti JXN-30

Company: Beckman Coulter
Catalog#: Avanti® JXN-30
Bio-protocol()
Company-protocol()
Other protocol()

Investigating the Assembly Status of the Plastid Encoded Polymerase Using BN-PAGE and Sucrose Gradient Centrifugation
Author:
Date:
2016-07-20
[Abstract]  The plastid encoded polymerase (PEP) represents a major transcription machinery in mature chloroplasts (Liere et al., 2011; Zhelyazkova et al., 2012). The proper assembly of this multi-subunit complex is important for plant growth and development (Pfalz and Pfannschmidt, 2013). The PEP polymerase can be purified from soluble and from membrane-bound (also named transcriptionally active chromosome, TAC) fractions. Blue Native polyacrylamide gel electrophoresis (BN-PAGE) and sucrose gradient sedimentation followed by immunoblot analyses is used to detect the status of the PEP complex assembly. [摘要]  质体编码聚合酶(PEP)代表成熟叶绿体中的主要转录机制(Liere等人,2011; Zhelyazkova等人,2012)。 这种多亚基复合物的正确装配对于植物生长和发育是重要的(Pfalz和Pfannschmidt,2013)。 PEP聚合酶可以从可溶性和膜结合(也称为转录活性染色体,TAC)级分中纯化。 蓝色使用天然聚丙烯酰胺凝胶电泳(BN-PAGE)和蔗糖梯度沉淀,随后进行免疫印迹分析来检测PEP复合物组装体的状态。

Comments