亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

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
  
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
精品人妻少妇一区二区三区在线,欧美色图另类图片,久久男人的天堂色偷偷
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-RAXL1/APC Conjugated antibody (bs-21124R-APC)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-21124R-APC
英文名稱 Rabbit Anti-RAXL1/APC Conjugated antibody
中文名稱 APC標記的視網(wǎng)膜前神經(jīng)折疊同源框蛋白抗體
別    名 ARMD6; CORD11; Macular degeneration, age related 6, included; MGC15631; Q50 type retinal homeobox; Q50-type retinal homeobox protein; QRX; rax2; RAX2_HUMAN; RAXL1; Retina and anterior neural fold homeobox like 1; Retina and anterior neural fold homeobox protein 2; Retina and anterior neural fold homeobox-like protein 1.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 神經(jīng)生物學  轉(zhuǎn)錄調(diào)節(jié)因子  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Chimpanzee, )
產(chǎn)品應用 ICC=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 21kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human RAXL1
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 homeodomain-containing protein that plays a role in eye development. Mutation of this gene causes age-related macular degeneration type 6, an eye disorder resulting in accumulations of protein and lipid beneath the retinal pigment epithelium and within the Bruch's membrane. Defects in this gene can also cause cone-rod dystrophy type 11, a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in loss of color vision and visual acuity, followed by the degeneration of rod photoreceptor cells, which progresses to night blindness and the loss of peripheral vision. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]

Function:
May be involved in modulating the expression of photoreceptor specific genes. Binds to the Ret-1 and Bat-1 element within the rhodopsin promoter.

Subcellular Location:
Nucleus.

DISEASE:
Defects in RAX2 are the cause of age-related macular degeneration type 6 (ARMD6) [MIM:613757]. ARMD is in most patients manifest as ophthalmoscopically visible yellowish accumulations of protein and lipid (known as drusen) that lie beneath the retinal pigment epithelium and within an elastin-containing structure known as Bruch's membrane. ARMD is likely to be a mechanistically heterogeneous group of disorders. Defects in RAX2 are the cause of cone-rod dystrophy type 11 (CORD11)
[MIM:610381]. CORD is characterized by the initial degeneration of cone photoreceptor cells, thus causing early loss of visual acuity and color vision, followed by the degeneration of rod photoreceptor cells and leading to progressive night blindness and peripheral visual field loss.

Similarity:
Contains 1 homeobox DNA-binding domain.

Database links:

Entrez Gene: 84839 Human

Omim: 610362 Human

SwissProt: Q96IS3 Human

Unigene: 532691 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權(quán)所有 2004-2026 www.www.chomd.com.cn 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
主站蜘蛛池模板: 久久久久久九九99精品人与狗合体| 337P日本欧洲噜噜噜噜| 日本zljzljzlj日本少妇| 久久96精品国产app| 77月天天看亚洲精品推荐| 无码永久免费AV网站巨乳| 国产一区三区三区看三区| 亚洲一线产区二线产区精华黄色视频| 日木AV无码专区亚洲AV毛片AI换脸| 精品久久久久久国产二线| 中文字幕人妻无码系列第三区韩| 丝袜美腿三区资源| 东北老妇露脸xXXXX| 婷婷热久久日AV片| 成人国产一区二区三区香焦精品| 亚洲高清国产拍精品嫩草影院,太粗太硬| 久久AV高潮AV无码AV喷吹,性生活久久久,久久午夜 | 精品国产一区二区三区无码流出 | 中文字幕无码乱人伦_国精品99| 色丝袜av咪咪咪咪| 999久久久免费精品国产大爆门| 日韩精品无码AV| 中文字幕无码久久久精密桃| 久久这里有精品视频农村人故事情节片黄色一维片 | 伊人蕉久影院212| 久久99精品久久久久久久不卡,欧美伊人色综合久久天天 | 无码专区免费视频00| 东京热本道成人欧美| 人妻少妇精品中文字幕av-| 91视频国产高清大学生| 久久天天躁狠狠躁夜夜爽蜜月2023| 99精品国产在热久久无毒不卡起碰2022国产 | 香蕉久久国产AV一区二区| 成人午夜免费A片在线播放| 日韩熟妇在线网址| 伊人久久精品一区二区三区78| 精品香蕉在线观看免费网站 | 国产成人久久久精品二区三区_亚洲伊人成| 中文字幕无码不卡一区二区三区,亚洲大道无码高清乱码 | 亚洲一区精品中文字幕无码| 国内少妇偷人精品视频免费_精品|