91精品少妇一区二区三区蜜桃臀,少妇搡BBBB搡BBB搡失恋,BBB片一毛片A片AA少妇,国产成人无码久久久久毛片朴信惠
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
少妇搡BBBB搡BBB搡造水爽,做爰特黄AAAAAAA片
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-C9orf72/RBITC Conjugated antibody (bs-8595R-RBITC)
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-8595R-RBITC
英文名稱 Rabbit Anti-C9orf72/RBITC Conjugated antibody
中文名稱 羅丹明(RBITC)標記的9號染色體開放閱讀框72抗體
別    名 chromosome 9 open reading frame 72; CI072_HUMAN; MGC23980; Uncharacterized protein C9orf72.  
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  染色質(zhì)和核信號  神經(jīng)生物學  轉(zhuǎn)錄調(diào)節(jié)因子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human, Mouse, Rat,  (predicted: Chicken, Dog, Pig, Cow, Horse, )
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 53kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human C9orf72
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:
Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf72 gene product has been provisionally designated C9orf72 pending further characterization. There are two isoforms of C9orf72 that are produced as a result of alternative splicing events.

Subcellular Location:
Cytoplasm. Nucleus. Note=Detected in the cytoplasm of neurons from post mortem brain tissue (PubMed:21944778). Detected in the nucleus in fibroblasts (PubMed:21944779).

Tissue Specificity:
Both isoforms are widely expressed, including kidney, lung, liver, heart, testis and several brain regions, such as cerebellum. Also expressed in the frontal cortex and in lymphoblasts (at protein level).

DISEASE:
Defects in C9orf72 are the cause of frontotemporal dementia and/or amyotrophic lateral sclerosis (FTDALS) [MIM:105550]. An autosomal dominant neurodegenerative disorder characterized by adult onset of frontotemporal dementia and/or amyotrophic lateral sclerosis in an affected individual. There is high intrafamilial variation. Frontotemporal dementia is characterized by frontal and temporal lobe atrophy associated with neuronal loss, gliosis, and dementia. Patients exhibit progressive changes in social, behavioral, and/or language function. Amyotrophic lateral sclerosis is characterized by the death of motor neurons in the brain, brainstem, and spinal cord, resulting in fatal paralysis. Note=Caused by a large expansion of a GGGGCC hexanucleotide within the first C9orf72 intron located between the first and the second non-coding exons. The expansion leads to the loss of transcription of one of the two transcripts encoding isoform 1 and to the formation of nuclear RNA foci.

Database links:

Entrez Gene: 203228 Human

Entrez Gene: 73205 Mouse

Entrez Gene: 313155 Rat

Omim: 614260 Human

SwissProt: Q96LT7 Human

SwissProt: Q6DFW0 Mouse

SwissProt: Q66HC3 Rat

Unigene: 493639 Human

Unigene: 331544 Mouse

Unigene: 233897 Rat



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 rvdoil.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
久久一级毛片内射人妖 | 91精品国产乱码久久蜜臀 | 国产成人视频在线观看 | 91精品国产情侣高潮 | 91在线精品无码秘 入口软件 | 久久天天躁狠狠躁夜夜躁2014 | 一级黄色免费在线观看 | 昏睡迷奷无码片免费A片 | 国产农村妇女一级A片免 | 蜜桃av色偷偷av老熟女 | 免费中文字幕日韩欧美 | 无码人妻丰满熟妇啪啪欧美 | 欧美疯狂做受XXXX猛交 | 国产精品欲AV蜜臀 | 一区二区三区在线电影 | 久久国产乱子伦精品一区二区小说 | 近親相姦中出し親子中文字幕 | 天堂资源在线观看 | 国产精品嫩草影院久久久 | 最近2019中文字幕 | 国产一级a毛一级a看免费视频乱 | 性猛交乱妇免费看A片 | 欧美成人3D精品性动漫 | 国产一级a一级a免费视频 | 大乳爆乳午夜A∨片91 | 国产乡下妇女做爰视频 | 成人国产精品秘 鲁鲁3D | 91口爆吞精国产水多多 | 欧美性爱激情一区二区三区 | 国产野外做爰A片视频 | 波多野结衣AV片免费观看 | 看真人BBBB视频 | 99国产精品在线观看 | 91中文人妻在线在线精品 | 人妻毛片A一级毛片免费看 亚州精品一区二区三区黄久 | 91精品国产高清一区二区三区蜜臀 | 国产熟女真实乱精品视频 | 久久久WWW成人免费精品 | 88欧美狠狠噜日日噜噜 | 国产精品18久久久久久首页狼 | 国产一区精品在线观看 |