產(chǎn)品編號 | bs-21039R-PE |
英文名稱 | Rabbit Anti-ROGDI/PE Conjugated antibody |
中文名稱 | PE標記的亮氨酸拉鏈結(jié)構(gòu)域蛋白ROGDI抗體 |
別 名 | FLJ22386; KTZS; Leucine zipper domain protein; Protein rogdi homolog; rogdi; rogdi homolog (Drosophila); rogdi, Drosophila, homolog of; ROGDI_HUMAN. |
規(guī)格價格 | 100ul/2980元 購買 大包裝/詢價 |
說 明 書 | 100ul |
研究領(lǐng)域 | 細胞生物 發(fā)育生物學 神經(jīng)生物學 細胞周期蛋白 轉(zhuǎn)錄調(diào)節(jié)因子 激酶和磷酸酶 |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應 | (predicted: Human, Mouse, Rat, Pig, Cow, Sheep, ) |
產(chǎn)品應用 | ICC=1:50-200 IF=1:50-200
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
分 子 量 | 32kDa |
性 狀 | Lyophilized or Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human ROGDI |
亞 型 | IgG |
純化方法 | affinity purified by Protein A |
儲 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
保存條件 | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
產(chǎn)品介紹 |
background: This gene encodes a protein of unknown function. Loss-of-function mutation in this gene cause Kohlschutter-Tonz syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012] Function: May act as a positive regulator of cell proliferation. Subcellular Location: Nucleus. Tissue Specificity: Widely expressed with highest levels in spinal cord, brain, heart and bone marrow. Also expressed in fetal brain and liver. DISEASE: The disease is caused by mutations affecting the gene represented in this entry. Disease description:An autosomal recessive disorder characterized by severe global developmental delay, early-onset intractable seizures, spasticity, and amelogenesis imperfecta affecting both primary and secondary teeth and causing yellow or brown discoloration of the teeth. Although the phenotype is consistent, there is variability. Intellectual disability is related to the severity of seizures, and the disorder can thus be considered an epileptic encephalopathy. Some infants show normal development until seizure onset, whereas others are delayed from birth. The most severely affected individuals have profound mental retardation, never acquire speech, and become bedridden early in life. Similarity: Belongs to the rogdi family. Database links: Entrez Gene: 79641 Human Entrez Gene: 66049 Mouse Omim: 614574 Human SwissProt: Q9GZN7 Human SwissProt: Q3TDK6 Mouse Unigene: 459795 Human Unigene: 27792 Mouse Unigene: 995 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
1、抗體溶解方法 | |
2、抗體修復方式 | |
3、常用試劑的配制 | |
4、免疫組化操作步驟 | |
5、免疫組化問題解答 | |
6、Western Blotting 操作步驟 | |
7、Western Blotting 問題解答 | |
8、關(guān)于肽鏈的設(shè)計 | |
9、多肽的溶解與保存 | |
10、酶標抗體效價測定程序 | |
| 麻豆蜜桃69无码专区 | 国产精品国产精品国产 | 国产亚洲精品成人a v久久网站 | 国产黄A级三级三级三级破解 | 国产xx899av在线观看 | 本田岬高潮一区二区三区 | 日本区欧美区亚洲区 | 少妇特黄A一区二区三区 | 91午夜夜伦鲁鲁片无码影视 | 乌克兰一级婬片A片AAA视频 | 国产又爽 又黄 免费 | 国产乱码精品一区二区三区四川人 | 国模精品无码一区二区免费蜜桃 | 国产成人精品 水 国产成人精品AA毛片 | 黄色视频一直看一直爽 | 一级片免费在线观看视频 | 乳欲人妻奶水3-5 | 91成人影库一级A片Al | 国产精品 国产17 | 成人无码特级视频在线观看 | 中国老妇女爽到高潮 | 免费观看欧美特级黄色片 | 国产一二三精品无码不卡 | 91亚洲精品久久久蜜桃 借种 | 日本国产成人亚洲精品无码 | 人妻偷国产网曝门91 | 蜜臀久久国产精品伦子伦 | 西西444WWW无码视频男男 | 亚洲中文一区二区 | 导管无码毛片av在线 | www.黄色视频在线观看 | 放荡寡妇欧美一级A片红桃视频 | 狠狠色婷婷久久综合频道日韩小说 | 日韩成人AV网站 | 无码精品人妻一区二区三区影院 | 国产农村精品无套内谢 | 国产性猛交普通话对白 | 蜜臀AV999无码精品国产专区 | 真实乱视频国产免费观看 | 日韩A V免费在线 |