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           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
88国产精品欧美一区二区三区三,亚洲午夜国产片在线观看,日本精品一区二区三区高清
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-RBM10/PE-Cy5.5 Conjugated antibody (bs-19762R-PE-Cy5.5)
訂購熱線:400-901-9800
訂購郵箱:sales@www.p2b3.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@www.p2b3.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-19762R-PE-Cy5.5
英文名稱 Rabbit Anti-RBM10/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5標記的RNA結(jié)合蛋白10抗體
別    名 DXS8237E; G patch domain containing protein 9; G patch domain-containing protein 9; GPATC9; GPATCH9; HGNC9896; KIAA0122; MGC1132; MGC997; Rbm10; RBM10_HUMAN; RNA binding motif protein 10; RNA binding protein 10; RNA binding protein S1-1; RNA-binding motif protein 10; RNA-binding protein 10; RNA-binding protein S1-1; S1-1; TARPS; ZRANB5.  
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  結(jié)合蛋白  表觀遺傳學(xué)  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Pig, Cow, Rabbit, Sheep, )
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 103kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human RBM10
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 nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2011]

Function:
May be involved in post-transcriptional processing, most probably in mRNA splicing. Binds to RNA homopolymers, with a preference for poly(G) and poly(U) and little for poly(A).

Subunit:
Associates with the spliceosome. Component of a large chromatin remodeling complex, at least composed of MYSM1, PCAF,RBM10 and KIF11/TRIP5.

Subcellular Location:
Nucleus. In the extranucleolar nucleoplasm constitutes hundreds of nuclear domains, which dynamically change their structures in a reversible manner. Upon globally reducing RNA polymerase II transcription, the nuclear bodies enlarge and decrease in number. They occur closely adjacent to nuclear speckles or IGCs (interchromatin granule clusters) but coincide with TIDRs.

Post-translational modifications:
Phosphorylated upon DNA damage, probably by ATM or ATR.

DISEASE:
Defects in RBM10 are the cause of TARP syndrome (TARPS) [MIM:311900]. It is a disorder characterized by the Robin sequence (micrognathia, glossoptosis and cleft palate), talipes equinovarus and cardiac defects.

Similarity:
Contains 1 C2H2-type zinc finger.
Contains 1 G-patch domain.
Contains 1 RanBP2-type zinc finger.
Contains 2 RRM (RNA recognition motif) domains.

Database links:

Entrez Gene: 8241 Human

Entrez Gene: 236732 Mouse

Omim: 300080 Human

SwissProt: P98175 Human

SwissProt: Q99KG3 Mouse

Unigene: 401509 Human

Unigene: 279194 Mouse

Unigene: 383632 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.www.p2b3.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
插女生那个的视频| 午夜十八禁福利亚洲一区二区| 激烈18禁高潮视频免费| 97超级免费视频在线观看| 无码人妻精品一区二区三区蜜桃| 国产精品视频美熟女一区二区| 国产情侣色综合久久有码| 亚洲国产区男人本色| 插到底啊啊啊视频| 国产亚洲精品一区久久| 9亚洲导航深夜福利亚洲| 黑人大鸡把操逼视频| 中文字幕在线观一二三区| 大男人在线无码直播| 精品人妻一区二区三区日产乱码| 国产情侣色综合久久有码| 啊灬啊别停灬用力啊男男在线观看| 国产 日韩 亚洲 一区| 白丝袜子宫啊啊啊不要了| 在线 中文字幕 第一页| 大鸡扒干美女BB直流水| 精品精品国产一区二区性色av| 久久99国产中文| 国产天美传媒剧免费观看| 狂插美女大屁股在线观看| 亚洲乱熟女一区二区三区| 精品免费福利片国产| 精品日本一区二区三区视频播放| 一个色综合色综合色综合| 国产激情内射免费精品| 美女被插入小穴爆操视频| 国产成人亚洲精品在线看| 91video国产一区| 国产精品一区二区在线观看91| 色老头av亚洲三区三区| 国产成人AV剧情| 久久久18禁一区二区网| 操我好舒服用力视频| 中文字幕乱码人妻一区二区三区| 国产熟女视频一区二区三区| 波多野吉衣吹潮Av|