吃奶呻吟打开双腿做受动态图 -亚洲色偷偷色噜噜狠狠99网-日韩精品极品视频在线观看免费-来一水AV@lysav

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  人才招聘  關(guān)于我們  聯(lián)系我們
jizz日本,CHINESE熟女老女人HD
Rabbit Anti-NPC1/PE Conjugated antibody (bs-6764R-PE)
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@xucheq.com
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-6764R-PE
英文名稱1 Rabbit Anti-NPC1/PE Conjugated antibody
中文名稱 PE標(biāo)記的尼曼匹克C1前體蛋白抗體
別    名 Niemann Pick C1; Niemann Pick C1 protein precursor; Niemann Pick disease, type C1; Niemann-Pick C1 protein; NPC; NPC1; NPC1_HUMAN.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 心血管  細(xì)胞生物  神經(jīng)生物學(xué)  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Mouse,  (predicted: Human, Rat, Chicken, Pig, Guinea Pig, )
產(chǎn)品應(yīng)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 138kDa
細(xì)胞定位 細(xì)胞膜 
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from mo NPC1/Niemann Pick C1
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 large protein that resides in the limiting membrane of endosomes and lysosomes and mediates intracellular cholesterol trafficking via binding of cholesterol to its N-terminal domain. It is predicted to have a cytoplasmic C-terminus, 13 transmembrane domains, and 3 large loops in the lumen of the endosome - the last loop being at the N-terminus. This protein transports low-density lipoproteins to late endosomal/lysosomal compartments where they are hydrolized and released as free cholesterol. Defects in this gene cause Niemann-Pick type C disease, a rare autosomal recessive neurodegenerative disorder characterized by over accumulation of cholesterol and glycosphingolipids in late endosomal/lysosomal compartments.[provided by RefSeq, Aug 2009].

Function:
Involved in the intracellular trafficking of cholesterol. May play a role in vesicular trafficking in glia, a process that may be crucial for maintaining the structural and functional integrity of nerve terminals.

Subunit:
Interacts with TMEM97.

Subcellular Location:
Late endosome membrane; Multi-pass membrane protein. Lysosome membrane; Multi-pass membrane protein.

Post-translational modifications:
Glycosylated.

DISEASE:
Defects in NPC1 are the cause of Niemann-Pick disease type C1 (NPC1) [MIM:257220]. A lysosomal storage disorder that affects the viscera and the central nervous system. It is due to defective intracellular processing and transport of low-density lipoprotein derived cholesterol. It causes accumulation of cholesterol in lysosomes, with delayed induction of cholesterol homeostatic reactions. Niemann-Pick disease type C1 has a highly variable clinical phenotype. Clinical features include variable hepatosplenomegaly and severe progressive neurological dysfunction such as ataxia, dystonia and dementia. The age of onset can vary from infancy to late adulthood. An allelic variant of Niemann-Pick disease type C1 is found in people with Nova Scotia ancestry. Patients with the Nova Scotian clinical variant are less severely affected.

Similarity:
Belongs to the patched family.
Contains 1 SSD (sterol-sensing) domain.

Database links:

Entrez Gene: 4864 Human

Entrez Gene: 18145 Mouse

Entrez Gene: 266732 Rat

Omim: 607623 Human

SwissProt: O15118 Human

SwissProt: O35604 Mouse

Unigene: 464779 Human

Unigene: 715623 Human

Unigene: 3484 Mouse



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

尼曼匹克病-神經(jīng)磷沉積性疾病,主要是由于神經(jīng)磷脂酶(sphingomyelinase)缺乏所致,神經(jīng)鞘磷脂酶(sphingomyelinase)缺乏致神經(jīng)鞘磷脂代謝障礙。導(dǎo)致后者蓄積在單核巨噬細(xì)胞系統(tǒng)內(nèi),出現(xiàn)肝、脾腫大,中樞神經(jīng)系統(tǒng)退行性變。神經(jīng)鞘磷脂是由N-酰鞘氨醇與一個分子的磷酸膽鹼(phosphocholine)在C1、部位連接而成,神經(jīng)鞘磷脂來源于各種細(xì)胞膜和紅細(xì)胞基質(zhì)等。在細(xì)胞代謝衰老過程中被巨噬細(xì)胞吞噬,神經(jīng)磷脂酶缺少后,全身神經(jīng)鞘磷脂代謝紊亂,神經(jīng)磷脂沉積在單核-巨噬細(xì)胞系統(tǒng)和神經(jīng)組織細(xì)胞中。
版權(quán)所有 2004-2026 www.xucheq.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
特级BBBBBBBBB视频| 国产丰满老熟妇乱XXX1区| WC凹凸撒尿间谍女厕HD| 亚洲色婷婷一区二区三区| 欧美精品在线观看| 国产爆乳无码一区二区麻豆| 免费看又黄又无码的网站| 国产女人AAA级久久久级| 国产内射爽爽大片视频社区在线| 熟妇人妻无乱码中文字幕| 无码无套少妇毛多18PXXXX| 学长被C哭着爬走又被拉回来| 新婚娇妻陪局长出差BD| 苍井そら无码av| 久久精品国产精品亚洲毛片| 亚洲AV无码乱码精品国产| 日本无码小泬粉嫩精品图| 国产精品51麻豆CM传媒| 无码人妻一区二区三区免费N鬼沢 久久精品色妇熟妇丰满人妻5O | 亚洲精品国产精品乱码不99| 欧美疯狂做受XXXXX高潮| 亚洲色偷精品一区二区三区| 久久96国产精品久久久| 女人与公驹交酡全过程| 一本久道中文无码字幕AV| 国产免费AV片无码永久免费| 久久免费看少妇高潮A片| 西瓜在线看免费观看视频| 女人高潮真实叫床声MP3| 高H猛烈失禁潮喷A片在线观看| 少妇性饥渴无码A区免费| 乌克兰少妇XXXX做受野外| 国产精品美女WWW爽爽爽视频| 全免费A级毛片免费看视频| 国产成人精品免高潮在线观看| 久久黄色视频| 国产精品日日做人人爱| 国产精品Ⅴ无码大片在线看| 日本VA欧美VA精品发布| 日韩一区二区三区精品| 宝贝在街上把奶露出来H|