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| 产品编号 | bs-17279P |
| 英文名称 | SCE1 Antibody Blocking Peptide |
| 中文名称 | SCE1蛋白封闭多肽 |
| 英文别名 | AHUS5; AT3G57870; ATSCE1; EMB1637; SCE1_ARATH; EMBRYO DEFECTIVE 1637; SCE1A; SUMO CONJUGATING ENZYME 1A; SUMO CONJUGATION ENZYME 1; SUMO ligase. |
| 纯化方法 | HPLC |
| 研究领域 | Cell Biology > Other Antibodies > Plant related targets Cell Biology > Proteolysis / Ubiquitin > Proteasome / Ubiquitin > Sumo |
| 亚基 | Interacts with SIZ1 (via PHD domain) and MMS21. |
| 相似性 | Belongs to the ubiquitin-conjugating enzyme family. |
| 功能 | SUMO-conjugating enzyme accepts the SUMO proteins from the E1 SUMO-activating heterodimer SAE1/SAE2 and catalyzes its covalent attachment to other proteins with the E3 SUMO ligases SIZ1 and MMS21. It associates with SIZ1 for sumoylation of the transcription factor GTE3. |
| 保存条件 | Shipped at 4℃. Stored at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 注意事项 | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| 背景资料 | Encodes a SUMO liagse that directs the attachment of the small protein SUMO to target proteins via an isopeptide bond. This enzyme is localized to the nucleus and plants with reduced levels of this protein show higher sensitivity to ABA in root growth inhibition assays. It has high similarity to the yeast UBC9 SUMO ligase and is sometimes referred to by that name. |
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文献和实验or from the literature are missing. In this article, processing parameters for DNA, peptide, antibody, and carbohydrate microarrays are outlined. The applicability of the model experiments is demonstrated and described in detail on the example of short oligonucleotides.
Synthesis and Probing of Membrane-bound Peptide Arrays
the stringency of the blocking conditions and make sure that the primary binding partner and detection reagent (e.g., antibody) are of high purity and are used in the highest possible dilution. Stage
Mapping Protein‐Protein Interactions with Phage‐Displayed Combinatorial Peptide Libraries
. Fack, F., Deroo, S., Kreis, S., and Muller, C.P. 2000. Heteroduplex mobility assay (HMA) pre‐screening: An improved strategy for the rapid identification of inserts selected from phage‐displayed peptide
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