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  聯系我們
亚洲狠狠色丁香婷婷综合,午夜三级a三级三点在线观看 ,中文字幕人妻丝袜美腿乱
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-AHI1/PE-Cy3 Conjugated antibody (bs-7854R-PE-Cy3)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-7854R-PE-Cy3
英文名稱 Rabbit Anti-AHI1/PE-Cy3 Conjugated antibody
中文名稱 PE-Cy3標記的白血病相關蛋白AHI1抗體
別    名 Abelson helper integration site 1 protein homolog; Abelson helper integration site 1; Abelson helper integration site; AHI 1; AHI-1; Ahi1; AHI1_HUMAN; Contatins SH3 and WD40 domains; JBTS3; Jouberin; ORF1.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 細胞生物  細胞周期蛋白  細胞分化  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
產品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 137kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human AHI1
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:
Highly expressed in the most primitive normal hematopoietic cells. Expressed in brain, particularly in neurons that give rise to the crossing axons of the corticospinal tract and superior cerebellar peduncles. Expressed in kidney (renal collecting duct cells) (at protein level).
Involvement in disease:Defects in AHI1 are the cause of Joubert syndrome type 3 (JBTS3) . JBTS is an autosomal recessive disorder presenting with cerebellar ataxia, oculomotor apraxia, hypotonia, neonatal breathing abnormalities and psychomotor delay. Neuroradiologically, it is characterized by cerebellar vermian hypoplasia/aplasia, thickened and reoriented superior cerebellar peduncles, and an abnormally large interpeduncular fossa, giving the appearance of a molar tooth on transaxial slices (molar tooth sign). Additional variable features include retinal dystrophy and renal disease. JBTS3 shows minimal extra central nervous system involvement and appears not to be associated with renal dysfunction.

Function:
Component of the tectonic-like complex, a complexlocalized at the transition zone of primary cilia and acting as abarrier that prevents diffusion of transmembrane proteins betweenthe cilia and plasma membranes (By similarity).

Subunit:
Part of the tectonic-like complex (also named B9complex). Interacts with MKS1 (By similarity). Interacts withNPHP1.

Subcellular Location:
Cytoplasm, cytoskeleton, cilium basal body(By similarity). Cell junction, adherens junction.

Tissue Specificity:
Highly expressed in the most primitive normalhematopoietic cells. Expressed in brain, particularly in neuronsthat give rise to the crossing axons of the corticospinal tract andsuperior cerebellar peduncles. Expressed in kidney (renalcollecting duct cells) (at protein level).

DISEASE:
Defects in AHI1 are the cause of Joubert syndrome type 3(JBTS3) [MIM:608629]. JBTS is an autosomal recessive disorderpresenting with cerebellar ataxia, oculomotor apraxia, hypotonia,neonatal breathing abnormalities and psychomotor delay.Neuroradiologically, it is characterized by cerebellar vermianhypoplasia/aplasia, thickened and reoriented superior cerebellarpeduncles, and an abnormally large interpeduncular fossa, givingthe appearance of a molar tooth on transaxial slices (molar toothsign). Additional variable features include retinal dystrophy andrenal disease. JBTS3 shows minimal extra central nervous systeminvolvement and appears not to be associated with renaldysfunction.

Similarity:
Contains 1 SH3 domain.
Contains 7 WD repeats.

Database links:

Entrez Gene: 54806 Human

Entrez Gene: 52906 Mouse

Entrez Gene: 308923 Rat

Omim: 608894 Human

SwissProt: Q8N157 Human

SwissProt: Q8K3E5 Mouse

SwissProt: Q6DTM3 Rat

Unigene: 386684 Human

Unigene: 253280 Mouse

Unigene: 155144 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

腦組織表達
版權所有 2004-2026 www.www.chomd.com.cn 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
主站蜘蛛池模板: 亚洲精品福利网站爽| 99精品国产综合久久久久五月天网页版 | 一区 二区 三区 中文字幕视频| 国产亚洲精品无码专区-久久国产欧美日韩| 日日狠狠久久偷偷色综合45蜜桃 | 91精品国产自产91精品资源,色综合久久无码| 国产综合一区二区在线观看户外导航| 精品97国产免费人成视频|中文h综| 免费观看黄色的网站,一区二区三区级二级三级| 亚洲精品美女网站国自产| 亚洲人成未满十八禁网站_第11集| 一本色道无码道DVD在线播放直播| 一色屋精品视频在线观看17c视频在线观看 | 一区二区三区视频网站| 欧美激情999自慰| 蜜臀AⅤ国产精品久久久国产老师| 国产成人yy视频一区二区 | 老熟妇精品无码视频在线播放| 成年美女黄网站色大片不卡下载| av中文字幕网站有码| 四虎影视在线视频国产传媒视频 | 亚洲一区二区三区久久久久免| 亚洲中文精品久久久久久不卡 - 三十 | 五十路熟女中出撮kkh| 亚洲乱色伦图片小说精品国产一区二区三区久久精品 | 中国护士18XXXXHD少妇| 亚洲日韩人人吃瓜| 精品久久综合1区2区3区激情红桃视频| 好大好深好爽视频97| 亚洲精品美女久久久久99图片爸妈45岁| 久久精品午夜一区二区福利,水牛| 国产在线观看激情四| 亚洲国产成人综合精品亚洲日韩一 | 视频在线一区二区三区四区播放| 老太业余BB大全视频 | 婷婷国产天堂久久五月天| jyzz16日本老师在线喷水| 亚洲综合国产成人丁香五月激情免费高清精品av| 男女一进一出抽搐免费视频大全网站| 中文字幕无乱码高清视频在线看 | 2021国产麻豆剧果冻传媒入口爱情公寓 |