超碰97自拍_久久99久久98精品免观看软件_在线亚洲一区_九九视频这里只有精品_国产精品一区二区欧美视频_精品国产区一区

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
日本黄色片免费,视频一区中文,欧美性猛交99久久久久99按摩
首頁 > 產品中心 > 一抗 > 產品信息
RSPH4A Rabbit pAb (bs-11472R)  
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
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價

產品編號 bs-11472R
英文名稱 RSPH4A Rabbit pAb
中文名稱 Kartagener綜合征相關蛋白RSHL3抗體
別    名 CILD11; dJ412I7.1; Radial spoke head protein 4 homolog A; Radial spoke head-like protein 3; RSH4A_HUMAN; RSHL3; Rsph4a; RSPH6B; A230081C05.  
研究領域 細胞生物  發育生物學  神經生物學  信號轉導  細胞骨架  細胞外基質  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應 Human,Mouse (predicted: Rat,Pig,Sheep,Cow,Chicken,Dog,Horse)
產品應用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 81 kDa
檢測分子量
細胞定位 細胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human RSPH4A/RSHL3: 435-482/716 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 RSHL3 is predicted to be a component of the radial spoke head based on homology with proteins in the biflagellate alga Chlamydomonas reinhardtii and other ciliates. RSHL3 (radial spoke head-like protein 3), also known as radial spoke head protein 4 homolog A, is a 716 amino acid protein that belongs to the flagellar radial spoke RSP4/6 family. Mutations in the RSHL3 gene cause primary ciliary dyskinesia 1, a disease arising from dysmotility of motile cilia and sperm. Existing as three alternatively spliced isoforms, the RSHL3 gene contains 6 exons, is conserved in chimpanzee, dog, cow, mouse, rat, chicken, zebrafish, fruit fly and P.falciparum, and maps to human chromosome 6q22.1.

Function:
Probable component of the axonemal radial spoke head. Radial spokes are regularly spaced along cilia, sperm and flagella axonemes. They consist of a thin stalk which is attached to a subfiber of the outer doublet microtubule, and a bulbous head which is attached to the stalk and appears to interact with the projections from the central pair of microtubules.

Subcellular Location:
Cytoplasm; cytoskeleton; cilium axoneme. Radial spoke.

Tissue Specificity:
Defects in RSPH4A are the cause of primary ciliary dyskinesia type 11 (CILD11) [MIM:612649]. CILD is an autosomal recessive disorder characterized by axonemal abnormalities of motile cilia. Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia; reduced fertility is often observed in male patients due to abnormalities of sperm tails. Half of the patients exhibit situs inversus, due to dysfunction of monocilia at the embryonic node and randomization of left-right body asymmetry. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome.

DISEASE:
Defects in RSPH4A are the cause of primary ciliary dyskinesia type 11 (CILD11) [MIM:612649]. CILD is an autosomal recessive disorder characterized by axonemal abnormalities of motile cilia. Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia; reduced fertility is often observed in male patients due to abnormalities of sperm tails. Half of the patients exhibit situs inversus, due to dysfunction of monocilia at the embryonic node and randomization of left-right body asymmetry. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome.

Similarity:
Belongs to the flagellar radial spoke RSP4/6 family.

SWISS:
Q5TD94

Gene ID:
345895

Database links:

Entrez Gene: 345895 Human

Omim: 612647 Human

SwissProt: Q5TD94 Human

Unigene: 160380 Human



Kartagener綜合征:由下列三聯癥組成,支氣管擴張、鼻竇炎或鼻息肉及內臟反位(主要是右位心)。若僅具備內臟反位及支氣管擴張兩項,則為不全性Kartagener綜合征。常合并其他先天性畸形。其病因是由于全身纖毛先天性缺乏軸絲臂,引起纖毛活動力喪失、黏液纖毛運輸功能障礙,分泌物和細菌潴留而發生持續性感染長期存在所致。以學齡兒童及青少年多發,有家族史。主要癥狀為隨年齡加重的咳嗽、咳痰和咯血,晨起明顯,易患感冒及肺炎,常見體征為發紺和杵狀指。
產品圖片
Sample: Trachea (Mouse) Lysate at 40 ug Primary: Anti-RSPH4A? (bs-11472R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 81 kD Observed band size: 81 kD
Sample: Lung (Mouse) Lysate at 40 ug A431(Human) Cell Lysate at 30 ug Testis (Mouse) Lysate at 40 ug Primary: Anti-RSPH4A? (bs-11472R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 81 kD Observed band size: 81 kD
版權所有 2004-2026 www.ggggww.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: 亚洲天堂在线视频播放 | 亚洲AV无码成H人动漫无遮挡 | 日本一区精品视频 | 日韩精品成人网 | 欧美日韩特级黄片观看 | 在线观看中文字幕一区二区 | 强●媚薬レズ狂いatid543 | 已婚丰满少妇21P | 少妇高潮太爽了在线观看欧美 | 欧美黑人XXXⅩ高潮交 | 91天天色 | 黄色大片播放 | 水蜜桃免费视频 | 国产成人精品三级在线 | 亚洲人成在线观看无码 | a在线亚洲男人的天堂在线 大地资源网视频观看免费高清 | 精品自拍最新换脸综合网站 | 少妇毛片久久久久久久久 | 亚洲视频二区 | 暖暖在线日本免费中文 | 国产麻豆一区 | 国产群交影片在线播放 | 国产精品无码日韩欧 | 欧美最猛性xxxxx亚洲精品 | 国产成人鲁色资源国产91色综 | 波多野结衣乳巨码无在线播放 | 久久国产精品_国产精品 | jizz大全日本护士喷奶水 | 国产高清视频色欲 | 99热久RE这里只有精品小草 | 办公室少妇激情呻吟a片在线观看 | 亚洲热视频在线观看 | 四虎免费在线 | 国产乡下妇女三片 | 少妇富婆一区二区三区夜夜 | 国产精品高潮在线 | 国产欧美综合一区二区三区 | 色戒网址 | 永夜星河短剧免费观看 | 91婷婷| 中国帅小伙gaysextubevideo |