强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
掃碼關(guān)注公眾號(hào)           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  關(guān)于我們  聯(lián)系我們
草1024榴社区入口成人小说,四川BBB搡BBB爽爽爽电影
Rabbit Anti-NF-H/PE-Cy5.5 Conjugated antibody (bs-0708R-PE-Cy5.5)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-0708R-PE-Cy5.5
英文名稱 Rabbit Anti-NF-H/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5標(biāo)記的高分子量神經(jīng)絲蛋白抗體
別    名 Neurofilament 200; 200 kDa neurofilament protein; 200 kD Neurofilament Heavy; NEFH; NEFH; NF200; NF-200; Neurofilament H; Neurofilament heavy polypeptide 200kD; Neurofilament heavy polypeptide 200kDa; Neurofilament heavy polypeptide; Neurofilament triplet H protein; Neurofilament triplet H protein; Hypophosphorylated Neurofilament H; NF H; NFH; NFH_HUMAN; KIAA0845.  
規(guī)格價(jià)格 100ul/2980元 購買        大包裝/詢價(jià)
說 明 書 100ul  
研究領(lǐng)域 細(xì)胞生物  神經(jīng)生物學(xué)  信號(hào)轉(zhuǎn)導(dǎo)  細(xì)胞凋亡  轉(zhuǎn)錄調(diào)節(jié)因子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Mouse,  (predicted: Human, Rat, )
產(chǎn)品應(yīng)用 Flow-Cyt=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 118kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human NF-H
亞    型 IgG
純化方法 affinity purified by Protein A
儲(chǔ) 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:
Neurofilaments can be defined as the intermediate or 10nm filaments found in specifically in neuronal cells. When visualised using an electron microscope, neurofilaments appear as 10nm diameter fibres of indeterminate length that generally have fine wispy protrusions from their sides. They are particularly abundant in axons of large projection neurons. They probably function to provide structural support for neurons and their synapses and to support the large axon diameters required for rapid conduction of impulses down axons. Neurofilaments are composed of a mixture of subunits, which usually includes the three neurofilament triplet proteins neurofilament light (NFL), neurofilament medium (NFM) and neurofilament heavy (NFH). Neurofilaments may also include smaller amounts of peripherin, alpha internexin, nestin and in some cases vimentin. Antibodies to the various neurofilament subunits are very useful cell type markers since the proteins are among the most abundant of the nervous system, are expressed only in neurons, and are biochemically very stable. Some studies have shown that levels of neurofilament heavy and neurofilament light are elevated in patients with Alzheimer's disease, frontotemporal lobe dementia, and vascular dementia.

Function:
Neurofilaments usually contain three intermediate filament proteins: L, M, and H which are involved in the maintenance of neuronal caliber. NF-H has an important function in mature axons that is not subserved by the two smaller NF proteins.

Post-translational modifications:
There are a number of repeats of the tripeptide K-S-P, NFH is phosphorylated on a number of the serines in this motif. It is thought that phosphorylation of NFH results in the formation of interfilament cross bridges that are important in the maintenance of axonal caliber.
Phosphorylation seems to play a major role in the functioning of the larger neurofilament polypeptides (NF-M and NF-H), the levels of phosphorylation being altered developmentally and coincident with a change in the neurofilament function.
Phosphorylated in the Head and Rod regions by the PKC kinase PKN1, leading to inhibit polymerization.

DISEASE:
Defects in NEFH are a cause of susceptibility to amyotrophic lateral sclerosis (ALS) [MIM:105400]. ALS is a neurodegenerative disorder affecting upper and lower motor neurons, and resulting in fatal paralysis. Sensory abnormalities are absent. Death usually occurs within 2 to 5 years. The etiology is likely to be multifactorial, involving both genetic and environmental factors.

Similarity:
Belongs to the intermediate filament family.

Database links:

Entrez Gene: 4744 Human

Entrez Gene: 380684 Mouse

Entrez Gene: 24587 Rat

Omim: 162230 Human

SwissProt: P12036 Human

SwissProt: P19246 Mouse

SwissProt: P16884 Rat

Unigene: 198760 Human

Unigene: 298283 Mouse

Unigene: 108194 Rat



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 nmgps.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(hào): 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(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
国产精品久久久久久久久无码春色 | 四季Av夜夜嗨噜噜噜蜜臀 | 捆绑羞辱调教一二三区 | 日韩特黄特色大片免费一级 | 91精品国产综合久久久久久漫画 | 国产女伦精品一区二区三区级 | 在线观看国产高清黄色视频 | 导管无码毛片av在线 | 凪光巨乳人妻一区二区在线 | 蜜桃视频免费在线观看 | 午夜yy一区二区三区伦 | 白丝拔腿自慰爽出白浆 | 国产无遮挡又黄又爽免费网站 | 麻豆 视频在线观看免费 | 亚洲AV久久无码秘 原神 | 婷婷国产亚洲精品网站 | 欧美色视频在线观看免费 | 黄色视频网站在线观看推荐 | 91蜜臀精品国产自偷在线 | 极品少妇一区二区三区 | 青青草原免费在线视频 | 国产91 丝袜在线观看 | 亚洲中文字幕在线无码 | 色情无码AⅤ苍井空 | 国产人妻久久爽无码 | 午夜精品秘 一区二区三区 中文字幕av久久爽一区 | 2019AV在线视频 | 精品人人搡人妻人人玩A片 国产免费观看黄色电视网站 | 少妇性色午夜婬片AAA片软件 | 亚洲中文字幕在线无码 | 国产A级一级视频免费看 | 亚洲短视频无码在线观看 | 亚州乱伦AV一二三区 | 国内又黄又硬又大的视频 | JlZZJlZZ国产精品久久 | 亚洲秘 无码一区小野夕子 天津熟女露脸91熟女人妻 | 蜜桃秘 av一站二站三站 | 少妇看黄色一级二级性生活高朝 | 大乳爆乳午夜A∨片91 | 久久成人无码国产免费播放 | 免费一级无码婬片A片 |