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
国产精品成人国产乱一区,内捧疯狂进出免费视频,四lll少妇BBBB槡BBBB
Rabbit Anti-VCP/BF350 Conjugated antibody (bs-1443R-BF350)
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-1443R-BF350
英文名稱 Rabbit Anti-VCP/BF350 Conjugated antibody
中文名稱 BF350標(biāo)記的含纈酪肽蛋白抗體
別    名 valosin-containing protein; 15S Mg(2+) ATPase p97 subunit; ATPase p97; IBMPFD; MGC131997; MGC148092; MGC8560; p97; TER ATPase; TERA; transitional endoplasmic reticulum ATPase; valosin-containing protein; VCP; yeast Cdc48p homolog; Transitional endoplasmic reticulum ATPase; TER ATPase; 15S Mg(2+)-ATPase p97 subunit; p97.  
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 腫瘤  神經(jīng)生物學(xué)  信號(hào)轉(zhuǎn)導(dǎo)  生長(zhǎng)因子和激素  糖尿病  糖蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Dog, Cow, Horse, )
產(chǎn)品應(yīng)用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 97kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human VCP
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:
The protein encoded by this gene is a member of a family that includes putative ATP-binding proteins involved in vesicle transport and fusion, 26S proteasome function, and assembly of peroxisomes. This protein, as a structural protein, is associated with clathrin, and heat-shock protein Hsc70, to form a complex. It has been implicated in a number of cellular events that are regulated during mitosis, including homotypic membrane fusion, spindle pole body function, and ubiquitin-dependent protein degradation. [provided by RefSeq, Jul 2008]

Function:
Necessary for the fragmentation of Golgi stacks during mitosis and for their reassembly after mitosis. Involved in the formation of the transitional endoplasmic reticulum (tER). The transfer of membranes from the endoplasmic reticulum to the Golgi apparatus occurs via 50-70 nm transition vesicles which derive from part-rough, part-smooth transitional elements of the endoplasmic reticulum (tER). Vesicle budding from the tER is an ATP-dependent process. The ternary complex containing UFD1L, VCP and NPLOC4 binds ubiquitinated proteins and is necessary for the export of misfolded proteins from the ER to the cytoplasm, where they are degraded by the proteasome. The NPLOC4-UFD1L-VCP complex regulates spindle disassembly at the end of mitosis and is necessary for the formation of a closed nuclear envelope (By similarity). Regulates E3 ubiquitin-protein ligase activity of RNF19A.

Subcellular Location:
Cytoplasm > cytosol. Nucleus. Present in the neuronal hyaline inclusion bodies specifically found in motor neurons from amyotrophic lateral sclerosis patients. Present in the Lewy bodies specifically found in neurons from Parkinson disease patients.

Post-translational modifications:
Phosphorylated by tyrosine kinases in response to T-cell antigen receptor activation (By similarity).
Phosphorylated upon DNA damage, probably by ATM or ATR. ISGylated.

DISEASE:
Defects in VCP are the cause of inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (IBMPFD) [MIM:167320]; also known as muscular dystrophy, limb-girdle, with Paget disease of bone or pagetoid amyotrophic lateral sclerosis or pagetoid neuroskeletal syndrome or lower motor neuron degeneration with Paget-like bone disease. IBMPFD features adult-onset proximal and distal muscle weakness (clinically resembling limb girdle muscular dystrophy), early-onset Paget disease of bone in most cases and premature frontotemporal dementia.

Similarity:
Belongs to the AAA ATPase family.

Database links:

Entrez Gene: 7415 Human

Entrez Gene: 269523 Mouse

Entrez Gene: 116643 Rat

Omim: 601023 Human

SwissProt: P55072 Human

SwissProt: Q01853 Mouse

SwissProt: P46462 Rat

Unigene: 529782 Human

Unigene: 245976 Mouse

Unigene: 98891 Rat



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

含纈酪肽蛋白(VCP即p97),是一種廣泛存在的膜結(jié)合糖蛋白,在細(xì)胞活性中有著廣泛的功能,其特點(diǎn)是作為類似分子伴侶的作用在內(nèi)質(zhì)網(wǎng)相關(guān)的蛋白降解及細(xì)胞周期調(diào)控中起到重要作用,VCP蛋白可以和肝素在細(xì)胞表面結(jié)合,而起到保護(hù)細(xì)胞的作用。
目前對(duì)VCP的表達(dá)水平與食道癌、胃癌、結(jié)、直腸癌、肝癌、胰腺癌等消化系統(tǒng)惡性腫瘤等是研究的熱點(diǎn)。
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)
一区二区三区无码在线 | 小黄书成人版免费视频网站 | 国内精品人妻无码久久久影院蜜桃 | 国产性情成人网站av | 性爱一级片免费观看 | 国产精品熟女一区二区不卡 | 欧洲精品一区二区 | 久久久久亚洲精品无码蜜桃 | 四川寡妇BBB搡BBB爽爽爽 | 人人妻人人澡人人爽精品欧美 | 国产+无码+精品十欧美 | 97人妻人人澡人人爽人国产 | 亚洲一区二区三区在线观看视频 | 91极品炮架口爆吞精 | 粉嫩av婬片一区二区三区 | 日本一区四区免费播放 | 无码动漫精品一区二区三区 | 91精品人妻一区二区三区蜜桃 | 91大神一区二区三区日韩 | 91 国产丝袜在线播放竹菊 | 四川黄色视频网站www | 91精品国产综合久久久不卡98口 | 日韩欧美性爱在线播放 | 日韩视频在线免费观看 | 91精品无码久久久久久久 | 丰满老女人A片免费观看 | 亚洲精品成人区在线观看 | 夜夜春极品少妇操出白浆 | 奶头大的一级A片一级 | 嫩呦国产一区二区三区AV | 少妇大叫太粗太大爽一区二区 | 91亚洲国产成人久久精品麻豆 | 中文字幕永久区乱码六区 | 国产一二三精品无码不卡 | 国产成人91亚洲精品无码观看 | 国产有大有粗有黄的视频 | 好爽又高潮了毛片免费下载 | 中文字幕永久哔哔免费播放 | 91精品无码久久久久久久 | 成人午夜啪免费视频在线观看软件 | 成全老司机黄色视频 |