吃奶呻吟打开双腿做受动态图 -亚洲色偷偷色噜噜狠狠99网-日韩精品极品视频在线观看免费-来一水AV@lysav

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
欧美性受XXXX白人性爽,国产国语老龄妇女a片
Rabbit Anti-PRPF8/BF350 Conjugated antibody (bs-19405R-BF350)
訂購(gòu)熱線(xiàn):400-901-9800
訂購(gòu)郵箱:sales@xucheq.com
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@xucheq.com
說(shuō) 明 書(shū): 100ul  
100ul/2980.00元
大包裝/詢(xún)價(jià)
產(chǎn)品編號(hào) bs-19405R-BF350
英文名稱(chēng)1 Rabbit Anti-PRPF8/BF350 Conjugated antibody
中文名稱(chēng) BF350標(biāo)記的mRNA前體剪接因子PRPF8抗體
別    名 220 kDa U5 snRNP specific protein; 220 kDa U5 snRNP-specific protein; Apoptosis regulated protein 1; Apoptosis regulated protein 2; HPRP8; p220; Pre mRNA processing factor 8; Pre mRNA-processing factor 8, S. cerevisiae, homolog of; Pre-mRNA-processing-splicing factor 8; Precursor mRNA processing protein; PRP8; PRP8 homolog; PRP8 pre mRNA processing factor 8 homolog; PRP8_HUMAN; PRPC8; Prpf8; Retinitis pigmentosa 13 (autosomal dominant); RP13; SNRNP220; Splicing factor Prp8; U5 snRNP specific protein (220 kD), ortholog of S. cerevisiae Prp8p; U5 snRNP specific protein.  
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)  干細(xì)胞  結(jié)合蛋白  表觀(guān)遺傳學(xué)  
抗體來(lái)源 Rabbit
克隆類(lèi)型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rhesus monkey, Gorilla, Orangutan, Xenopus tropicalis)
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 274kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human PRPF8
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:
Pre-mRNA splicing occurs in 2 sequential transesterification steps. The protein encoded by this gene is a component of both U2- and U12-dependent spliceosomes, and found to be essential for the catalytic step II in pre-mRNA splicing process. It contains several WD repeats, which function in protein-protein interactions. This protein has a sequence similarity to yeast Prp8 protein. This gene is a candidate gene for autosomal dominant retinitis pigmentosa. [provided by RefSeq, Jul 2008]

Function:
Functions as a scaffold that mediates the ordered assembly of spliceosomal proteins and snRNAs. Required for the assembly of the U4/U6-U5 tri-snRNP complex. Functions as scaffold that positions spliceosomal U2, U5 and U6 snRNAs at splice sites on pre-mRNA substrates, so that splicing can occur. Interacts with both the 5' and the 3' splice site.

Subunit:
Part of the U5 snRNP complex. Component of the U4/U6-U5 tri-snRNP complex composed of the U4, U6 and U5 snRNAs and at least PRPF3, PRPF4, PRPF6, PRPF8, PRPF31, SNRNP200, TXNL4A, SNRNP40, DDX23, CD2BP2, PPIH, NHP2L1, EFTUD2, SART1 and USP39. Component of the U5.U4atac/U6atac snRNP complexes in U12-dependent spliceosomes. Found in a mRNA splicing-dependent exon junction complex (EJC) with SRRM1. Interacts with U5 snRNP proteins SNRP116 and SNRNP40. Interacts with EFTUD2 and SNRNP200. Interacts (via the MPN (JAB/Mov34) domain) with PRPF3 ('Lys-63'-linked polyubiquitinated); may stabilize the U4/U6-U5 tri-snRNP complex.

Subcellular Location:
Nucleus speckle.

Tissue Specificity:
Widely expressed.

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

DISEASE:
Defects in PRPF8 are the cause of retinitis pigmentosa type 13 (RP13) [MIM:600059]. RP leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. RP13 inheritance is autosomal dominant.

Similarity:
Contains 1 MPN (JAB/Mov34) domain.

Database links:

Entrez Gene: 10594 Human

Entrez Gene: 192159 Mouse

Entrez Gene: 287530 Rat

Omim: 607300 Human

SwissProt: Q6P2Q9 Human

SwissProt: Q99PV0 Mouse

Unigene: 181368 Human

Unigene: 3757 Mouse

Unigene: 106432 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 www.xucheq.com 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)
各种少妇正面着BBW撒尿视频| 琪琪婷婷五月色综合久久| 国产成人A亚洲精V品无码| 精品国产乱码久久久久久口爆| 日本夜爽爽一区二区三区| 99久久国产综合精品麻豆| 美女高潮黄又色高清视频免费| 欧美人妻日韩精品| 亚洲成AV人片在线观看无| 国产,日韩,丝袜,欧美一区| 欧美性受xxxx黑人xyx性爽 | 无码人妻精品中文字幕| 极品少妇被猛得白浆直流草莓视频 | 97人妻AV天天澡夜夜爽| 亚洲国产精品一区二区WWW| 18一20亚洲gay无套| 国产成A人亚洲精V品无码性色| 国产97色在线 | 日韩| 免费看又黄又无码的网站| 一性一交一口添一摸视频| 啊灬啊灬啊灬快灬高潮了女| 女人张开腿让男桶喷水高潮| 精品无码人妻一区二区免费蜜桃| 亚洲国产精品久久久久久久| 夜夜添无码一区二区三区| 亚洲av无码乱码在线观看性色| 狠狠躁18三区二区一区| 欧美亚洲色综久久精品国产 | 男人用嘴添女人下身免费视频| 精品丝袜人妻久久久久久| 色综合天天综合网国产成人网| 人人妻人人澡人人爽欧美一区| 国产精品沙发午睡系列990531| 国产亚洲精品精华液好用吗| 又大又紧又粉嫩18P少妇| 波多野结衣电影| 亚洲AV无一区二区三区久久| 国产AV无码专区亚洲AV毛片搜 | 午夜亚洲福利在线老司机| 波多野结衣乳巨码无在线观看 | 欧美日韩久久久精品A片|