日日操日日操,亚洲一区二区三区四区视频,成人午夜福利激情,无码中文7幕

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  關(guān)于我們  聯(lián)系我們
国产成人性生活视频网站,日本久久爱网址
Rabbit Anti-NDC1/PE-Cy7 Conjugated antibody (bs-19057R-PE-Cy7)
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 bs-19057R-PE-Cy7
英文名稱 Rabbit Anti-NDC1/PE-Cy7 Conjugated antibody
中文名稱 PE-Cy7標(biāo)記的跨膜蛋白48
別    名 nucleoporin NDC1; TMEM48; transmembrane protein 48; NET3.  
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  染色質(zhì)和核信號  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Cat, )
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 75kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human NDC1
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:
NDC1 is a 674 amino acid multi-pass membrane protein, central core structure of the nuclear pore complex (NPC) and member of the NDC1 family that is crucial for selective nuclear protein import. Existing as four alternatively spliced isoforms that are encoded by a gene located on human chromosome 1, NDC1 interacts with Nup35 and anchors Aladin to the nuclear envelope of the NPC, a region of macromolecular transport between the nucleus and cytoplasm. In the absence of NDC1, Aladin becomes mislocalized and may lead to the development of an autosomal recessive disorder termed achalasia-addisonianism-alacrima (triple A) syndrome. Triple A syndrome is characterized by achalasia, alacrima and adrenocortico-tropin-resistant adrenal insufficiency. Robust expression in neural systems associated with cognitive, motor and sensory functions is consistent with the myriad of symptoms experienced by patients with triple A syndrome.

Function:
Component of the nuclear pore complex (NPC), which plays a key role in de novo assembly and insertion of NPC in the nuclear envelope. Required for NPC and nuclear envelope assembly, possibly by forming a link between the nuclear envelope membrane and soluble nucleoporins, thereby anchoring the NPC in the membrane.

Subunit:
Interacts with the NUP35/NUP53 By similarity. Interacts with AAAS, anchoring it to the nuclear envelope.

Subcellular Location:
Nucleus; nuclear pore complex; multipass membrane protein

Similarity:
Belongs to the NDC1 family.

Database links:

Entrez Gene: 55706 Human

Entrez Gene: 72787 Mouse

Entrez Gene: 362557 Rat

Entrez Gene: 335236 Zebrafish

Omim: 610115 Human

SwissProt: Q9BTX1 Human

SwissProt: Q8VCB1 Mouse

SwissProt: Q6AXN4 Rat

SwissProt: Q7SZC5 Zebrafish



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 www.bklrv.cn 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
激情综合网五月激情,com| 日韩字幕在线精品天堂| 天天天日日日射射射| 少妇激情被擦| 久久伊人国产产免费精品在线| 中文字字幕在线中文乱码久草| 天美九一厂毛片| 精品久久德国| www欧美日韩黄| 国产区中午| 大鸡巴操小骚穴视频啊啊嗯哦哦| 美女被爆操麻豆| 亚洲美女精品网站| 久久精品人人爱人人爽| 色呦呦一区98| 国产AV日韩AV人人操| 久久久久久久久久婷婷婷婷婷婷婷| 日本久久cao| 日韩欧美爱爱亚洲| 大鸡巴操逼骨头骨头真过瘾视频| 国产欧美日韩bj视频免费| 亚洲乱伦中文字幕一区二区| 一区影院日韩| 欧美中文字幕日韩一区| 欧美日韩亚洲成人久久| 18狠狠躁夜夜躁人人| 久久综合网| 国产电影一久久久久| 日韩性爱一区二区视频| 美女在线www二区| 淫乱性综合视频| 中文字幕久久中文人妻字字幕| 欧美大尺度久久久| 十八禁视频免费观看网页| 亚洲欧美原创免费| www.久9久| 夫妻久久性视频| 不卡无码视| 老熟妇.com| 2019久久精品中文字幕无码一区| 91网福利67国产,亚洲|