产品编号 | bs-16418R |
英文名称 | ZNFX1 Rabbit pAb |
中文名称 | ZNFX1蛋白抗体 |
别 名 | KIAA1404; NFX1 type zinc finger containing protein 1; RP4-686N3.1404-002; Zinc finger, NFX1-type containing 1. |
研究领域 | 细胞生物 转录调节因子 锌指蛋白 表观遗传学 |
抗体来源 | Rabbit |
克隆类型 | Polyclonal |
交叉反应 | (predicted: Human,Mouse,Rat,Horse) |
产品应用 | IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
理论分子量 | 220 kDa |
检测分子量 | |
细胞定位 | 细胞核 |
性 状 | Liquid |
浓 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human ZNFX1: 1601-1700/1918 |
亚 型 | IgG |
纯化方法 | affinity purified by Protein A |
缓 冲 液 | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
保存条件 | Shipped at 4℃. Store 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. |
PubMed | PubMed |
产品介绍 |
ZNFX1 is a 1918 amino acid nuclear protein that is widely expressed and contains six NF-X1-type zinc fingers, which are presumed to function as zinc binding domains. The gene encoding ZNFX1 maps to human chromosome 20, which contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome. There are two isoforms of ZNFX1 that are produced as a result of alternative splicing events. Function: ZNFX1 is widely expressed in all tissues. There are two named isoforms. Tissue Specificity: Widely expressed. Similarity: Contains 6 NF-X1-type zinc fingers. SWISS: Q9P2E3 Gene ID: 57169 Database links: Entrez Gene: 57169 Human SwissProt: Q9P2E3 Human |
1、抗体溶解方法 | |
2、抗体修复方式 | |
3、常用试剂的配制 | |
4、免疫组化操作步骤 | |
5、免疫组化问题解答 | |
6、Western Blotting 操作步骤 | |
7、Western Blotting 问题解答 | |
8、关于肽链的设计 | |
9、多肽的溶解与保存 | |
10、酶标抗体效价测定程序 | |