强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯(lián)系我們
国产乱妇无码A片免费看视频小说,日韩A片一级无码免费 蜜桃,午夜福利1000
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-CD133/PE-Cy5.5 Conjugated antibody (bs-0395R-PE-Cy5.5)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-0395R-PE-Cy5.5
英文名稱 Rabbit Anti-CD133/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5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; CD133 antigen.  
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  細胞類型標志物  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human, Mouse,  (predicted: Rat, )
產品應用 Flow-Cyt=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
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 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, Mar 2009]

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

Entrez Gene: 60357 Rat

Omim: 604365 Human

SwissProt: O43490 Human

SwissProt: O54990 Mouse

Unigene: 614734 Human

Unigene: 6250 Mouse

Unigene: 144589 Rat



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。
經研究發(fā)現(xiàn)內皮細胞不能結合CD133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.
版權所有 2004-2026 nmgps.com 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫(yī)療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網安備110107000727號
黄色视频在线观看免费 | 亚洲国产高清视频在线观看 | 无码高清免费视频 | 少妇厨房呻吟 在线 | 色婷婷综合久久久中文字幕 | 国产日韩久久久久69影院 | 日本无码A片免费网站 | 国产成人无码精品久久久A 精品乱码一区内射人妻无码 | 国产成人无码精品久久一区二区 | 日本91又粗又猛又大爽又黄少妇 | 色狠狠色噜噜AV天堂五区消防 | 欧美人妻日韩精品 | 国产中韩高清无码2023 | 红桃视频乱码一区二区三区 | 6699国产精品在线 | 一级内射在线观看视频 | 人妻少妇被猛烈进入中文字幕 | 最新黄色视频在线播放 | 成人午夜在线视频 | 在线观看免费无码视频 | 精人妻无码一区二区三区 | 国内精品久久久久久久影视麻生 | 欧美一级特黄AA大片 | 又大又粗又硬又爽又黄毛片视频 | 国产精品国产高清国产 | 91久久精品一区二区三 | 久热高清在线视频 | 性感美女被艹黄色视频在线观看 | 人人妻人人澡人人爽精品欧美 | 五十老熟妇乱子伦免费章节 | 国产成人AV一区二区三区 | 黄色视频网站在线观看推荐 | 一级毛片在线看免费视频网站 | 性感女性黄色免费观看视频网站 | 成人天码区免费A片 | 嫩草鲁丝久久精品熟女 | 韩国黑寡妇一级毛片 | 免费AV在线播放 | 新妺妺窝窝777777野外 | 四季AV一区二区三区 | 免费看黄色视频网站 |