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- bs-16245P
- 2025年10月16日
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| 产品编号 | bs-16245P |
| 英文名称 | GIN1 Antibody Blocking Peptide |
| 中文名称 | GIN1蛋白封闭多肽 |
| 英文别名 | FLJ20125; GIN-1; GIN1; GIN1_HUMAN; Gypsy retrotransposon integrase-like protein 1; TGIN1; Ty3/Gypsy integrase 1; ZH2C2; Zinc finger H2C2 domain-containing protein. |
| 纯化方法 | HPLC |
| 亚细胞定位 | Contains 1 integrase catalytic domain. |
| 组织特异性 | Widely expressed. Also found in tumors originating from parathyroid gland, colon, stomach, bladder, uterus and prostate. |
| 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 | GIN1 is a 522 amino acid protein containing one integrase catalytic domain. Widely expressed, GIN1 is also found in tumors originating from parathyroid gland, colon, stomach, bladder, uterus and prostate. Three isoforms of GIN1 are produced by alternative splicing events. The gene encoding GIN1 maps to human chromsome 5q21.1. Chromosome 5 contains 181 million base pairs and comprises nearly 6% of the human genome. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. Treacher Collins syndrome, Cockayne syndrome and familial adenomatous polyposis are also associated with chromosome 5. |
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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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