91精品少妇一区二区三区蜜桃臀,少妇搡BBBB搡BBB搡失恋,BBB片一毛片A片AA少妇,国产成人无码久久久久毛片朴信惠
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  關(guān)于我們  聯(lián)系我們
国内精品人妻无码久久久影院蜜桃,91无码精品秘 入口网站
Rabbit Anti-CD133 antigen/Cy5.5 Conjugated antibody (bs-0209R-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(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號 bs-0209R-Cy5.5
英文名稱 Rabbit Anti-CD133 antigen/Cy5.5 Conjugated antibody
中文名稱 Cy5.5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.  
規(guī)格價(jià)格 100ul/2980元 購買        大包裝/詢價(jià)
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)胞表面分子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human,  (predicted: Mouse, Rat, Fruit Fly, )
產(chǎn)品應(yīng)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(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(gè)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CD 133的抗體。證實(shí)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(gè)表面標(biāo)志.
版權(quán)所有 2004-2026 www.rvdoil.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
91在线无码精品秘 入口竹美 | 人人摸视频在线播放 | 日韩 码波多野结衣秘书 | 午夜成人国产精品影视 | 专干老熟女300部合集 | 波多野结衣高潮狂喷hd玲奈 | 四房色播五月天激情电影 | 成人毛片18女人毛片免费不卡在线 | 欧美熟妇特黄视频播放 | 酒店露脸约干普通话 | 99久久无码一区人妻贼王 | 国产成人91亚洲精品无码观看 | 五月婷婷综合激情 | 在线观看av女大学生黑料 | 欧美一级特黄大片xyx性爽 | 仙踪林一级婬片A片 | 91精品人妻无码AⅤ毛片 | 安徽BBBBB视频BBB| 国产美女裸体无遮挡永久免费 | 67194熟妇在线观看 | 波多野吉衣一区二区三区 | 蜜桃AV首页在线观看 | 成人做爰免费视频免费看 | 国产成人一区二区三区 | 海南妇搡BBBB搡BBBB | 91一区二区三区在线观看 | 在线播放成人A片 网站 | 免费看黃色AAAA片 | 亚洲国产精彩中文乱码AV | 欧一美一黄一色一色一色 | 鲁鲁鲁鲁狠鲁一鲁爽爽爽 | 国产一级a毛一级a做免费图片 | 国产三级黄色性感毛片大全 | 亚洲无 码蜜桃精东美业 | 亚洲AV成人片色在线观看高潮 | 我把黑丝美女操喷水内射视频 | 一级特黄女人18毛片免费视频 | 91色老久久精品偷偷蜜臀 | 国产亲子乱婬一级A片 | 成人黄色三级片下体视频 | 国产一区二区三区四区在线观看 |