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- 2025年10月16日
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| 产品编号 | bs-17267P |
| 英文名称 | SCAND2 Antibody Blocking Peptide |
| 中文名称 | SCAND2蛋白封闭多肽 |
| 英文别名 | SCAN domain containing 2; SCAN domain containing protein 2; SCAND 2. |
| 纯化方法 | HPLC |
| 亚细胞定位 | Nuclear |
| 功能 | SCAND2 contains a SCAN domain, an 80 amino acid residue sequence with a L-X(6)-L motif at its core. This core is flanked by A, E, L, M, H and C residues that are frequently found in alpha-helices. The function of SCAND2 has not been determined. |
| 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 | SCAND2 is a 306 amino acid nuclear protein that may play a role in the mechanism of transcriptional regulation. SCAND2 contains one SCAN box domain and, unlike most SCAN box domain-containing proteins, is devoid of a C2H2-type zinc-finger domain. The SCAN box domain is a conserved leucine rich motif, approximately 60 amino acids in length, that participates in protein-protein interactions. The SCAND2 gene is a fusion gene created by the retropositioning of a PHD2 (also known as EGLN1) gene copy from chromosome 1 onto an ancestral SCAN zinc finger gene, followed by exon shuffling. The resulting SCAND2 gene product has an N-terminal SCAN domain and a C-terminus derived from the PHD2 gene. SCAND2 exists as 2 isoforms produced by alternative splicing. |
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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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