来一水AV@lysav|亚洲AV无码片VR一区二区三区 |国产亚洲精久久久久久无码|视色4se成人午夜精品久久

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
CHINESE中年熟妇FREE|亚洲中文字幕色二区|艳妇系列短篇500
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-CENPJ/PE-Cy5 Conjugated antibody (bs-13835R-PE-Cy5)
訂購熱線:400-901-9800
訂購郵箱:sales@73327.net
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@73327.net
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-13835R-PE-Cy5
英文名稱1 Rabbit Anti-CENPJ/PE-Cy5 Conjugated antibody
中文名稱 PE-Cy5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  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 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 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 www.73327.net 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
国产成品精品午夜视频| 无码AV中文一区二区三区桃花岛| 无码人妻精品一区二区三区9厂 | 亚洲欧洲日韩黄色大片网站| 日本三级片在线观看| 亚洲精品高清白浆久久久久久| 久久精品欧美精品日韩精| 私人影院播放器| 国产精品Ⅴ无码大片在线看| XXXXA特别高潮| 人妻在厨房被色诱 中文字幕| 一个人看的视频免费高清在线观看 | 无码人妻一区二区三区| 亚洲av无码精品色午夜| 双性精跪趴灌满H室友| 小SAO货水好多真紧H无码视频| 色呦呦网站日韩精品| 国产性生交XXXXX免费| 国产精品一区久久精品国产| 黄桃AV无码免费一区二区三区| 少妇特大毛BBW | 影音先锋乱伦小说| 日本JAPANESE熟睡人妻| 欧美日韩免费看视频| 国产精品18久久久久久VR| 亚洲精品97久久中文字幕无码| 日本一区二区三区免费观看电影| 一级欧美一级日韩视频| 新狼窝色AV性久久久久久| 中文字幕在线观看不卡一区| 国产精品一区二区码| 国产精品久久久久久三级精品| 无码八A片人妻少妇久久| 久久久久久久久久女黄久久久久久 | 色综合久久超碰色婷婷| 国产精久久久久久久| 午夜亚洲AV永久无码精品| 日本中文字幕在线视频播二区| 欧美精品一区二区少妇免费A片| 国产精品无码久久久久| 国产精品久久久久久白浆18 |