產品編號 | bs-20563R-HRP |
英文名稱 | Rabbit Anti-SOX10/HRP Conjugated antibody |
中文名稱 | 辣根過氧化物酶標記的轉錄因子SOX10抗體 |
別 名 | DOM; MGC15649; SOX 10; SOX10; SOX10_HUMAN; SRY (sex determining region Y) box 10; SRY box containing gene 10; SRY related HMG box gene 10; Transcription factor SOX 10; Transcription factor SOX-10; WS4. |
規(guī)格價格 | 100ul/2980元 購買 大包裝/詢價 |
說 明 書 | 100ul |
研究領域 | 細胞生物 免疫學 神經生物學 干細胞 細胞凋亡 表觀遺傳學 |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應 | Mouse, Rat, (predicted: Human, Dog, Pig, Cow, Rabbit, Sheep, ) |
產品應用 | WB=1:500-2000 ELISA=1:100-1000 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
分 子 量 | 50kDa |
性 狀 | Lyophilized or Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human SOX10 |
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. |
產品介紹 |
background: This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional activator after forming a protein complex with other proteins. This protein acts as a nucleocytoplasmic shuttle protein and is important for neural crest and peripheral nervous system development. Mutations in this gene are associated with Waardenburg-Shah and Waardenburg-Hirschsprung disease. [provided by RefSeq, Jul 2008] Function: Transcription factor that seems to function synergistically with the POU domain protein TST-1/OCT6/SCIP. Could confer cell specificity to the function of other transcription factors in developing and mature glia (By similarity). Subcellular Location: Cytoplasm. Nucleus Tissue Specificity: Expressed in fetal brain and in adult brain, heart, small intestine and colon. DISEASE: Defects in SOX10 are the cause of Waardenburg syndrome type 2E (WS2E) [MIM:611584]. WS2 is a genetically heterogeneous, autosomal dominant disorder characterized by sensorineural deafness, pigmentary disturbances, and absence of dystopia canthorum. The frequency of deafness is higher in WS2 than in WS1. Defects in SOX10 are a cause of Waardenburg syndrome type 4C (WS4C) [MIM:613266]; also known as Waardenburg-Shah syndrome. WS4C is characterized by the association of Waardenburg features (depigmentation and deafness) and the absence of enteric ganglia in the distal part of the intestine (Hirschsprung disease). Defects in SOX10 are a cause of Yemenite deaf-blind hypopigmentation syndrome (YDBHS) [MIM:601706]. YDBHS consists of cutaneous hypopigmented and hyperpigmented spots and patches, microcornea, coloboma and severe hearing loss. Another case observed in a girl with similar skin symptoms and hearing loss but without microcornea or coloboma is reported as a mild form of this syndrome. Defects in SOX10 are the cause of peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, and Hirschsprung disease (PCWH) [MIM:609136]; also called neurologic variant of Waardenburg-Shah syndrome. PCWH is a rare, complex and more severe neurocristopathy that includes features of 4 distinct syndromes: peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, and Hirschsprung disease. Similarity: Contains 1 HMG box DNA-binding domain. Database links: Entrez Gene: 6663 Human Entrez Gene: 20665 Mouse Omim: 602229 Human SwissProt: P56693 Human SwissProt: Q04888 Mouse Unigene: 376984 Human Unigene: 276739 Mouse Unigene: 10883 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、關于肽鏈的設計 | |
9、多肽的溶解與保存 | |
10、酶標抗體效價測定程序 | |
| 亚洲精品久久久久久久久久飞鱼 | 97人人妻人人添人人澡 | 91精品少妇一区二区三区蜜桃臀 | 真实亂伦XXXX性XXXX | 黄色视频高清在线免费观看 | 久久久久久久91 | 亚洲精品无码成人 | 色偷偷熟女人妻另类视频 | XXX乱岳熟妇C0m | 国产农村妇女一级A片麻豆手机版 | 极品销魂美女粉嫩小泬污黄视频 | 欧美一区二区三区麻豆 | 人人妻人人澡人人爽DVD | 欧美乱码熟妇色精精品 | 国产黃色A片三級三級三級狼狈 | 亚洲色图自拍少妇内射高潮 | 国产TS余喵喵咕噜在线播放 | 国产大学生一级A片 | 日本日日摸日日舔一区 | 国产精品理伦天美传媒 | 四川少妇性无套内谢 | 免费无码Av片在线观看网址 | 日韩人妻丰满无码区A片 | 亚洲AV爽爽香蕉久久影 | 国产黃色A片三級三級三級 国产91欧美成人A片男男 | 国产精品久久久久久久久久不10 | 五十路老熟妇一区二区三区 | 91/竹菊/国产熟女 | 红桃视频成人无码在线观看 | 国产人妻无码一区二区三区不卡 | 人善交vuesdi欧美3D | 亚洲天堂无码视频 | 国产精品无码日韩18 | a片视频免费在线观看 | 天天干夜夜骑狠狠爱 | 91国產乱老熟女 | 欧美一区二区鲁丝袜片 | 果冻传媒之漂亮人妻煮饭 | 国产做爰XXXⅩ高潮韩国 | 久久久久久久久福利视频 |