| 產(chǎn)品編號 | bs-7505R |
| 英文名稱(chēng) | Plakophilin 1 Rabbit pAb |
| 中文名稱(chēng) | 橋粒斑菲素蛋白1抗體 |
| 別 名 | B6P; Band 6 protein; Plakophilin 1(ectodermal dysplasia/skin fragility syndrome); PKP1_HUMAN. |
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Specific References (1) | bs-7505R has been referenced in 1 publications.
[IF=3.775] Xue Y et al. Chlorogenic acid attenuates cadmium-induced intestinal injury in Sprague–Dawley rats. Food Chem Toxicol. 2019 Aug 4;133:110751. WB ; Rat.
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| 研究領(lǐng)域 | 心血管 細胞生物 免疫學(xué) 神經(jīng)生物學(xué) 信號轉導 細胞粘附分子 細胞外基質(zhì) |
| 抗體來(lái)源 | Rabbit |
| 克隆類(lèi)型 | Polyclonal |
| 克 隆 號 | |
| 交叉反應 | (predicted: Human,Mouse,Rat,Rabbit,Pig,Cow,Dog,GuineaPig,Horse) |
| 產(chǎn)品應用 | WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 理論分子量 | 83 kDa |
| 檢測分子量 | |
| 細胞定位 | 細胞核 細胞膜 |
| 性 狀 | Liquid |
| 濃 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human Plakophilin 1: 31-130/726 |
| 亞 型 | IgG |
| 純化方法 | affinity purified by Protein A |
| 緩 沖 液 | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| 保存條件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 注意事項 | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| PubMed | PubMed |
| 產(chǎn)品介紹 |
Plays a role in formation of desmosomal plaques and is found in desmosomes of most simple and stratified epithelia. Not found in cell types that have non-epithelial desmosomes. Absent in fibroblasts and other connective tissue types, including sarcomas. Function: Seems to play a role in junctional plaques. Contributes to epidermal morphogenesis. Subcellular Location: Nucleus. Cell junction, desmosome. Note: Nuclear and associated with desmosomes. Tissue Specificity: Isoform 2 is widely expressed. Isoform 1 is expressed in stratified squamous, complex, glandular duct and bladder epithelia. DISEASE: Defects in PKP1 are the cause of ectodermal dysplasia-skin fragility syndrome (EDSFS) [MIM:604536]; also known as McGrath syndrome. Ectodermal dysplasia defines a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. EDSFS is characterized by features of both cutaneous fragility and congenital ectodermal dysplasia affecting abnormalities in other epithelia or tissues. Desmosomes in the skin are small and poorly formed with widening of keratinocyte intercellular spaces and perturbed desmosome/keratin intermediate filament interactions. Similarity: Belongs to the beta-catenin family. Contains 9 ARM repeats. SWISS: Q13835 Gene ID: 5317 Database links: UniProtKB/Swiss-Prot: Q13835.2 Entrez Gene: 5317 Human Entrez Gene: 18772 Mouse Omim: 601975 Human SwissProt: Q13835 Human SwissProt: P97350 Mouse Unigene: 497350 Human Unigene: 4494 Mouse
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