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           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
黄色视频免费看网站,国产精品久久久久久久久动漫,少妇被又大又粗又爽毛片久久黑人
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-CENPJ/AP Conjugated antibody (bs-13835R-AP)
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
產(chǎn)品編號 bs-13835R-AP
英文名稱 Rabbit Anti-CENPJ/AP Conjugated antibody
中文名稱 堿性磷酸酶(AP)標記的著絲粒蛋白J抗體
別    名 CENP-J; CENPJ; CENPJ_HUMAN; Centromere protein J; Centrosomal P4.1-associated protein; CPAP; LAG-3-associated protein; LAP; LIP1; LYST-interacting protein 1; MCPH6.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 細胞生物  神經(jīng)生物學  信號轉(zhuǎn)導(dǎo)  轉(zhuǎn)錄調(diào)節(jié)因子  細胞分化  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, )
產(chǎn)品應(yīng)用 WB=1:50-200 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 153kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CENPJ
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 protein that belongs to the centromere protein family. During cell division, this protein plays a structural role in the maintenance of centrosome integrity and normal spindle morphology, and it is involved in microtubule disassembly at the centrosome. This protein can function as a transcriptional coactivator in the Stat5 signaling pathway, and also as a coactivator of NF-kappaB-mediated transcription, likely via its interaction with the coactivator p300/CREB-binding protein. Mutations in this gene are associated with primary autosomal recessive microcephaly, a disorder characterized by severely reduced brain size and mental retardation. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Apr 2012]

Function:
Plays an important role in cell division and centrosome function by participating in centriole duplication. Inhibits microtubule nucleation from the centrosome.

Subcellular Location:
Cytoplasm > cytoskeleton > centrosome. Cytoplasm > cytoskeleton > centrosome > centriole. Localized within the center of microtubule asters. During centriole biogenesis, it is concentrated within the proximal lumen of both parental centrioles and procentrioles.

Post-translational modifications:
Phosphorylation at Ser-589 and Ser-595 by PLK2 is required for procentriole formation and centriole elongation. Phosphorylation by PLK2 oscillates during the cell cycle: it increases at G1/S transition and decreases during the exit from mitosis. Phosphorylation at Ser-595 is also mediated by PLK4 but is not a critical step in PLK4 function in procentriole assembly.

DISEASE:
Defects in CENPJ are the cause of microcephaly primary type 6 (MCPH6) [MIM:608393]. A disorder defined as a head circumference more than 3 standard deviations below the age-related mean. Brain weight is markedly reduced and the cerebral cortex is disproportionately small. Despite this marked reduction in size, the gyral pattern is relatively well preserved, with no major abnormality in cortical architecture. Primary microcephaly is further defined by the absence of other syndromic features or significant neurological deficits.
Defects in CENPJ are the cause of Seckel syndrome type 4 (SCKL4) [MIM:613676].
SCKL4 is a rare autosomal recessive disorder characterized by proportionate dwarfism of prenatal onset associated with low birth weight, growth retardation, severe microcephaly with a bird-headed like appearance, and mental retardation.

Similarity:
Belongs to the TCP10 family.

Database links:

Entrez Gene: 55835 Human

Entrez Gene: 219103 Mouse

Omim: 609279 Human

SwissProt: Q9HC77 Human

SwissProt: Q569L8 Mouse

Unigene: 513379 Human

Unigene: 533828 Human

Unigene: 741581 Human

Unigene: 212525 Mouse



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 m.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: 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
91人妻人人人人爽 | 无遮挡毛片免费观看视频 | 国产精品精品久久久久久 | 成人黄色视频网站免费看 | 91少妇人妻偷人网站 | 国产亲妺妺乱免费视频 | av一区二区在线观看 | 亚洲欧美色一区二区三区 | 91人妻人人澡人人爽人人精品一 | 苍井优成人AV在线 | 女人裸体视频一区二区三区 | 久久人妻精品色欲网站 | 亚洲无码国产精品 | 成人国产AV一级毛片无码 | 免费看污网站在线观看 | 亚洲 欧洲 偷拍 自拍 | 又大又粗又硬又大又爽少妇毛片 | 91熟女丨九色老女人 | 国产精品一区二区三区小说 | 亚洲一區二區三区久久久成人動漫 | 久久Y不卡人妻内射中出 | 又爽 又黄 免费网站97动漫 | 无套内射视频在线观看 | 美女性感黄色免费网站 | 午夜福利理论片高清在线美国人性 | 国产精品成人AAAA网站女吊丝 | AAA级无码肉欲免费看 | 午夜无码国产午夜 | 国产 浪潮AV性色Av演员 | 国产熟妇无码A片AAA毛片视频 | 久久精品亚洲精品国产欧美 | 中文字幕无码人妻在线视频 | 久久无码人妻一区二区三区午夜免费 | 朝桐光东京热无码中文在线 | 精品一区二区三区蜜臀 | 公侵犯人妻二区三区 | 亚洲一区二区在线播放 | 成人H精精一区二区无码 | 黄免费在线观看高清国产 | 在线视频福利你懂的 | 91人妻人人爽人人添夜夜爽直软件播 |