吃奶呻吟打开双腿做受动态图 -亚洲色偷偷色噜噜狠狠99网-日韩精品极品视频在线观看免费-来一水AV@lysav

掃碼關(guān)注公眾號           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  人才招聘  關(guān)于我們  聯(lián)系我們
欧美 变态 另类 人妖,校花玉腿缠腰娇喘迎合,久久久久99精品成人片直播
Rabbit Anti-CD133/PE-Cy3 Conjugated antibody (bs-0395R-PE-Cy3)
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@xucheq.com
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-0395R-PE-Cy3
英文名稱1 Rabbit Anti-CD133/PE-Cy3 Conjugated antibody
中文名稱 PE-Cy3標(biāo)記的造血干細(xì)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(lǐng)域 腫瘤  細(xì)胞生物  免疫學(xué)  干細(xì)胞  細(xì)胞類型標(biāo)志物  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human, Mouse,  (predicted: Rat, )
產(chǎn)品應(yīng)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(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, 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(xì)胞標(biāo)志物
一般認(rèn)為,VEGFR2(血管內(nèi)皮生長因子受體2)是HSCs(造血干細(xì)胞)的特異性的表面標(biāo)志。近來經(jīng)研究發(fā)現(xiàn)CD133分子是HSCs(造血干細(xì)胞)特異性標(biāo)志。CD133即AC133,是一個新發(fā)現(xiàn)的HSCs(造血干細(xì)胞)表面標(biāo)志,在HSCs(造血干細(xì)胞)分化成熟過程中,CD133的含量迅速降低。EPCs(血管內(nèi)皮前體細(xì)胞)區(qū)別于成熟內(nèi)皮細(xì)胞的主要標(biāo)志是CD133。
經(jīng)研究發(fā)現(xiàn)內(nèi)皮細(xì)胞不能結(jié)合CD133的抗體。證實分化成熟的內(nèi)皮細(xì)胞不具有CD133。這些說明CD133可以作為EPCs(血管內(nèi)皮前體細(xì)胞)區(qū)別于成熟內(nèi)皮細(xì)胞的一個表面標(biāo)志.
版權(quán)所有 2004-2026 www.xucheq.com 北京博奧森生物技術(shù)有限公司
通過國際質(zhì)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(zhì)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(wǎng)安備110107000727號
99久久久无码国产精品免费| 宝贝你的奶好大我想吃第一章| 四川丰满少妇被弄到高潮| 色戒完整版| 大肉大捧一进一出好爽视频| 国产精品久久久久9999| 久久久久亚洲AV无码专区| 欧美性xxxxx极品少妇| 欧美激情综合五月色丁香| 宝贝在街上把奶露出来H| 天堂资源最新在线| 久久中文字幕人妻熟AV女| 国产内射爽爽大片视频社区在线| 国产精品亚洲一区二区三区| 久久综合狠狠综合久久综合88| 国产精品99久久久久久人| 高潮A片WWW张柏芝陈冠希| 中文无码人妻有码人妻中文字幕| 国产69精品久久久久777| 亚洲成AV人片在线观看| 亚洲AV无码专区在线观看下载| 欧美影院| 亚洲色无码A片一区二区潘甜甜| 亚洲AV无码偷拍在线观看| 97精品国产手机| 后入内射无码人妻一区| 色婷婷综合久久久中文字幕| 亚洲AV天堂AV在线成人播放| 我把五十老女人弄高潮了| 啊轻点灬太粗嗯太深了用力| japanesehd熟女熟妇| 中文字幕被公侵犯的漂亮人妻 | 365天今时之欲| 国产欧美日韩A片免费软件| 国产99在线 | 欧美| 亚洲精品久久久口爆吞精| 乳尖乱颤娇喘连连A片在线观看| 久久久久亚洲AV成人片乱码| 国产免费又爽又色又粗视频| 肥老熟妇伦子伦456视频| 国产中老年妇女精品|