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  人才招聘  關于我們  聯系我們
婷婷五月综合缴情在线视频,国产精品久久国产精品99盘,国产萌白酱在线一区二区
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Rapsyn/BF555 Conjugated antibody (bs-19664R-BF555)
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-19664R-BF555
英文名稱1 Rabbit Anti-Rapsyn/BF555 Conjugated antibody
中文名稱 BF555標記的突觸受體相關蛋白43抗體
別    名 43 kD receptor associated protein of the synapse; 43 kda postsynaptic protein; 43 kDa receptor-associated protein of the synapse; Acetylcholine receptor associated 43 kda protein; Acetylcholine receptor-associated 43 kDa protein; CMS1D; CMS1E; MGC3597; RAPSN; RAPSN_HUMAN; RAPsyn; Receptor associated protein of the synapse 43kD; Receptor associated protein of the synapse; RING finger protein 205; RNF 205; RNF205.  
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  免疫學  神經生物學  細胞骨架  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Chicken, Xenopus laevis)
產品應用 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 38kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Rapsyn
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:
This gene encodes a member of a family of proteins that are receptor associated proteins of the synapse. The encoded protein contains a conserved cAMP-dependent protein kinase phosphorylation site, and plays a critical role in clustering and anchoring nicotinic acetylcholine receptors at synaptic sites by linking the receptors to the underlying postsynaptic cytoskeleton, possibly by direct association with actin or spectrin. Mutations in this gene may play a role in postsynaptic congenital myasthenic syndromes. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Apr 2011]

Function:
Thought to play some role in anchoring or stabilizing the nicotinic acetylcholine receptor at synaptic sites. It may link the receptor to the underlying postsynaptic cytoskeleton, possibly by direct association with actin or spectrin.

Subcellular Location:
Cell membrane. Cell junction > synapse > postsynaptic cell membrane. Cytoplasm > cytoskeleton. Cytoplasmic surface of postsynaptic membranes.

DISEASE:
Defects in RAPSN are a cause of congenital myasthenic syndrome with acetylcholine receptor deficiency (ACHRDCMS) [MIM:608931]. ACHRDCMS is a post-synaptic congenital myasthenic syndrome. Congenital myasthenic syndromes (CMS) are inherited disorders of neuromuscular transmission that stem from mutations in presynaptic, synaptic, or postsynaptic proteins. Postsynaptic disorders result from mutations in proteins forming the subunits of the muscle acetylcholine receptor (AChR). The kinetic abnormalities of AChR result in either prolonged ion channel activations that underlie 'slow-channel myasthenic syndromes' (SCCMS) or abbreviated channel activations that underlie the abnormally rapid decay of endplate currents in 'fast-channel syndromes' (FCCMS). ACHRDCMS is the third disorder associated with postsynaptic CMS which could result from mutations in the proteins forming the muscle AChR. Mutations underlying AChR deficiency cause a 'loss of function' and show recessive inheritance.
Defects in RAPSN are the cause of fetal akinesia deformation sequence (FADS) [MIM:208150]; also known as Pena-Shokeir syndrome type 1 or fetal akinesia sequence or arthrogryposis multiplex congenita with pulmonary hypoplasia. FADS is a rare condition characterized by decreased intrauterine fetal movement, congenital limb contractures, pulmonary hypoplasia, polyhydramnios and craniofacial abnormalities.

Similarity:
Belongs to the RAPsyn family.
Contains 1 RING-type zinc finger.
Contains 7 TPR repeats.

Database links:

Entrez Gene: 5913 Human

Entrez Gene: 19400 Mouse

Entrez Gene: 362161 Rat

Omim: 601592 Human

SwissProt: Q13702 Human

SwissProt: P12672 Mouse

Unigene: 81218 Human

Unigene: 1272 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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: w无码无码无码无码无遮扣扣扣扣扣扣扣扣扣 | 亚洲国产午夜电影在线入口免费观看| 国产一区二区精品久久岳√,99久久免费| 免费无遮挡无码永久视频潮喷 | 久久精品中文无码资源站_东京热这| 无码精品A∨在线观看无精华液| 亚洲人成色777777老人头 | 中文字幕中出在线av| 国产69熟妇xXX| 爆乳熟妇一区二区三区霸乳翔田千里| 中文无码精品一区二区三区神马影院午夜视频 | 亚洲制服丝袜一区10p| 一区二区三区在线播放视频下载地址| 中文字幕乱码免费视频永久无码| 五月天婷婷在线播放国产,国 | 888米奇影视四色影视四色影视四色影视四色 | 欧美性暴力变态做爱| 美女在线视频黄色欧美| 国产草莓视频在线观看免费|国产 国产超碰人人做人人爱,最新亚洲AV日韩AV二 | 少妇人妻一级A毛片无码九太网| 亚洲AV成人无码网站18禁在线男男 | 亚洲∧v久久久无码精品+色欲 | 三上悠亚久久精品Av| 美国av免费观看影片| 波多野结衣中文在线播放1区2区| 亚洲高清欧美字幕中山文香| 少妇啪啪叫爽AV| 啊别插了视频高清在线观看,学生妹一级J人 | 国产成人久久精品激情情深叉喔 | 2048亚洲精品国产y| 人妻引诱黑人的中文字幕电影| 男人资源在线观看Av| 91精品国产91热久久久久福利_一区二区国 | 蜜芽AV网站首页入口| 自拍亚洲一区二区三区在线| 夜色资源网站APP下载| 色偷偷成人视频免费播放网站| 成人午夜视频精品一区二区在线观看| 中文字幕丰满乱子伦无码专区无码人妻久久一区二区 | 国产电影午夜成年免费视频| AV?无码?高潮?白丝|