產(chǎn)品編號 | bs-0209R-PE |
英文名稱 | Rabbit Anti-CD133 antigen/PE Conjugated antibody |
中文名稱 | PE標記的造血干細胞抗原CD133抗體 |
別 名 | AC133; Antigen AC133; Hematopoietic stem cell antigen; hProminin; PROM1; Prominin I; Prominin like protein 1 precursor; Prominin mouse like 1; prominin1; PROML1; CD133; CORD12; MCDR2; MSTP061; PROML1; RP41; STGD4; PROM1_HUMAN. |
規(guī)格價格 | 100ul/2980元 購買 大包裝/詢價 |
說 明 書 | 100ul |
研究領域 | 腫瘤 細胞生物 免疫學 干細胞 細胞表面分子 |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應 | Human, (predicted: Mouse, Rat, Fruit Fly, ) |
產(chǎn)品應用 | Flow-Cyt=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 | 95kDa |
性 狀 | Lyophilized or Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human CD133 antigen |
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 pentaspan transmembrane glycoprotein. The protein localizes to membrane protrusions and is often expressed on adult stem cells, where it is thought to function in maintaining stem cell properties by suppressing differentiation. Mutations in this gene have been shown to result in retinitis pigmentosa and Stargardt disease. Expression of this gene is also associated with several types of cancer. This gene is expressed from at least five alternative promoters that are expressed in a tissue-dependent manner. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq]. Function: Binds cholesterol in cholesterol-containing plasma membrane microdomains. Proposed to play a role in apical plasma membrane organization of epithelial cells. During early retinal development acts as a key regulator of disk morphogenesis. Involved in regulation of MAPK and Akt signaling pathways. In neuroblastoma cells suppresses cell differentiation such as neurite outgrowth in a RET-dependent manner. Subunit: Interacts with CDHR1 and with actin filaments. Subcellular Location: Cell projection, cilium, photoreceptor outer segment. Isoform 1: Apical cell membrane; Multi-pass membrane protein. Cell projection, microvillus membrane; Multi-pass membrane protein. Note=Found in extracellular membrane particles in various body fluids such as cerebrospinal fluid, saliva, seminal fluid and urine. Tissue Specificity: Isoform 1 is selectively expressed on CD34 hematopoietic stem and progenitor cells in adult and fetal bone marrow, fetal liver, cord blood and adult peripheral blood. Isoform 1 is not detected on other blood cells. Isoform 1 is also expressed in a number of non-lymphoid tissues including retina, pancreas, placenta, kidney, liver, lung, brain and heart. Found in saliva within small membrane particles. Isoform 2 is predominantly expressed in fetal liver, skeletal muscle, kidney, and heart as well as adult pancreas, kidney, liver, lung, and placenta. Isoform 2 is highly expressed in fetal liver, low in bone marrow, and barely detectable in peripheral blood. Isoform 2 is expressed on hematopoietic stem cells and in epidermal basal cells (at protein level). Expressed in adult retina by rod and cone photoreceptor cells (at protein level). Post-translational modifications: Isoform 1 and isoform 2 are glycosylated. DISEASE: Defects in PROM1 are the cause of retinitis pigmentosa type 41 (RP41) [MIM:612095]; also known as retinal degeneration autosomal recessive prominin-related. RP is a retinal dystrophy belonging to the group of pigmentary retinopathies. RP is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. Defects in PROM1 are the cause of cone-rod dystrophy type 12 (CORD12) [MIM:612657]. CORD12 is an inherited retinal dystrophy characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration. This leads to decreased visual acuity and sensitivity in the central visual field, followed by loss of peripheral vision. Severe loss of vision occurs earlier than in retinitis pigmentosa. Defects in PROM1 are the cause of Stargardt disease type 4 (STGD4) [MIM:603786]. Stargardt disease is the most common hereditary macular degeneration. It is characterized by decreased central vision, atrophy of the macula and underlying retinal pigment epithelium, and frequent presence of prominent flecks in the posterior pole of the retina. Defects in PROM1 are the cause of retinal macular dystrophy type 2 (MCDR2) [MIM:608051]. MCDR2 is a bull's-eye macular dystrophy characterized by bilateral annular atrophy of retinal pigment epithelium at the macula. Similarity: Belongs to the prominin family. Database links:
Entrez Gene: 8842 Human Entrez Gene: 19126 Mouse SwissProt: O43490 Human SwissProt: O54990 Mouse
Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. 干細胞標志物 一般認為,VEGFR2(血管內皮生長因子受體2)是HSCs(造血干細胞)的特異性的表面標志。近來經(jīng)研究發(fā)現(xiàn)CD133分子是HSCs(造血干細胞)特異性標志。CD133即AC133,是一個新發(fā)現(xiàn)的HSCs(造血干細胞)表面標志,在HSCs(造血干細胞)分化成熟過程中,CD133的含量迅速降低。EPCs(血管內皮前體細胞)區(qū)別于成熟內皮細胞的主要標志是CD133。 經(jīng)研究發(fā)現(xiàn)內皮細胞不能結合CD 133的抗體。證實分化成熟的內皮細胞不具有CD133。這些說明CD133可以作為EPCs(血管內皮前體細胞)區(qū)別于成熟內皮細胞的一個表面標志. |
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 | |
| 一区二区三区久久 | 五十路近親相姦中出し親子 | 日韩三级片一二三区在线观看狼友永久网址 | 国产女团裸体无遮挡A片 | 精品无码久久18 | 国产午夜AV中文字幕 | 波多野结衣高清性隶A片 | 91熟女丨九色老女人 | 日本五十路熟妇视频 | 日韩人妻无码精品一区二区 | 欧美精品久久久久 | 亚洲精品AA片在线无码 | 亚洲精品网站一区二区三 | 人人妻人人玩人人澡人人爽 | 国产美女无遮挡裸永久观看 | 在线观看黄色免费网站 | 37p粉嫩大胆色噜噜噜 | 欧一美一性一交一乱一性一 | 安徽妇搡BBBB搡BBBB一 | 欧美乱战大交XXXXX | 亚洲小说区图片区 | 99久久99久久精品國產片果凍 | 爱爱视频在线免费观看 | 免费无码婬片AAAA片直播表情 | 人妻中文字幕在线观看 | 欧美黑人猛插性爱视频 | 欧美熟妇搡BBB搡BBB | 国产毛多水多女人A片 | 99久久无码一区人妻A片红豆 | 三级片在线播放国产三区 | 8x8ⅹ拔擦拨擦免费入口 | 国产亲子乱婬一级A片 | 秘 亚洲国产精品成人网站 肥老熟妇伦子伦456视频 | 国产伦精品一区二区三区免费视频 | 91久久精品无码视频 | 99re在线视频播放 | 99久久久久久久久久 | 日本少妇AA一级特黄大片 | 国产欧美一区二区三区特黄手机版 | 二区三区日韩成人AV |