mm1313亚洲精品,欧美俄罗斯40老熟妇,欧美日韩在线观看视频在线,亚洲欧美国产激情综合在线

掃碼關(guān)注公眾號(hào)           掃碼咨詢(xún)技術(shù)支持           掃碼咨詢(xún)技術(shù)服務(wù)
  
客服熱線(xiàn):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
中文亚洲欧美乱码在线观看,黄色av美女免费网站,久久精品亚洲欧美日韩精品中文字幕
Rabbit Anti-CENPJ/PE Conjugated antibody (bs-13835R-PE)
訂購(gòu)熱線(xiàn):400-901-9800
訂購(gòu)郵箱:sales@m.p2b3.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@m.p2b3.cn
說(shuō) 明 書(shū): 100ul  
100ul/2980.00元
大包裝/詢(xún)價(jià)
產(chǎn)品編號(hào) bs-13835R-PE
英文名稱(chēng)1 Rabbit Anti-CENPJ/PE Conjugated antibody
中文名稱(chēng) PE標(biāo)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(jià)格 100ul/2980元 購(gòu)買(mǎi)        大包裝/詢(xún)價(jià)
說(shuō) 明 書(shū) 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)  轉(zhuǎn)錄調(diào)節(jié)因子  細(xì)胞分化  
抗體來(lái)源 Rabbit
克隆類(lèi)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(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:
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.m.p2b3.cn 北京博奧森生物技術(shù)有限公司
通過(guò)國(guó)際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書(shū)編號(hào): 00124Q34771R2M/1100
通過(guò)國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書(shū)編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
国产黄色三级三级三级看三级| 久久久久久久久久久久久久久久久久久| 亚洲1区2区3区av| 日韩欧美一级视频观看| 色婷婷久久久久久久久久| 激情久久三级视频网站| 久久久久久久久久久久久久久久久久久| 哪里有免费黄色av| 国产爽的冒白浆的视频| 亚洲欧美日韩国产精品专区| 日本伊人久久精品视频| 日本一区二区三区免费的视频| 欧美日韩国产成人精品自拍视频| 日韩熟女精品一区二区三区| 97国产精品国偷自产在线| 一区二区久久久久久久久| 99在线中文字幕一区| 国产亚洲视频中文字幕97精品| 亚洲中文av中文字幕在线| 日韩精品一区二区三区视频最新| 亚洲影视一区二区三区| 国产精品观看不卡视频| 精品日韩一区二区电影| 久久久精品熟女亚洲av麻豆| 欧美日韩在线看免费看成人| 欧美日韩一区二区三区大片在线观看| 国产av剧情亚洲精品| 99久久精品视香蕉蕉| 日本在线观看黄视频| 午夜福利国产观看视频1| 亚洲天堂网2020| 夜鲁夜鲁在线视频维| 欧美激情a成人综合亚洲综合| 日本午夜福利在线视频| 欧美午夜激情久久久久| 国产精品久久久久粉嫩小| 日韩欧美一区二区在线播放视频| 黄色网色网色网色网色网站| 日韩久久精品一区二区三区介绍| 五月婷婷六月丁香免费视频| 亚洲国产精品久久久久网站|