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  人才招聘  關(guān)于我們  聯(lián)系我們
欧美av成人在线视频,亚洲中文字幕无码永久在线,日本一区二区免费在线看
首頁 > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
Rabbit Anti-ITPRIPL1  antibody (bs-17187R)  
訂購熱線:400-901-9800
訂購郵箱:sales@m.p2b3.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@m.p2b3.cn
說明書: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價

產(chǎn)品編號 bs-17187R
英文名稱 Rabbit Anti-ITPRIPL1  antibody
中文名稱 ITPRIPL1蛋白抗體
別    名 Inositol 1,4,5 triphosphate receptor interacting protein like 1; IPIL1; KIAA1754 like; KIAA1754L.  
研究領(lǐng)域 細(xì)胞生物  免疫學(xué)  通道蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human,Mouse (predicted: Rat,Sheep,Cow,Dog,Horse)
產(chǎn)品應(yīng)用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 61kDa
細(xì)胞定位 細(xì)胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ITPRIPL1: 25-100/555 <Extracellular>
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 ITPRIPL1 is a 555 amino acid protein belonging to the ITPRIP family. ITPRIPL1 is a single-pass type I membrane protein expressed as two isoforms produced by alternative splicing events. The gene that encodes ITPRIPL1 maps to human chromosome 2, the second largest human chromosome, consisting of 237 million bases encoding over 1,400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr鰉 syndrome is due to mutations in the ALMS1 gene. It has been hypothesized that human chromosome 2 is the result of an ancient fusion of two ancestral chromosome due to its composition of a vestigial second centromere and vestigial telomeres.

Function:
The function remains unknown. There are two named isoforms.

Subcellular Location:
Membrane; Single-pass type I membrane protein

Similarity:
Belongs to the ITPRIP family.

SWISS:
Q6GPH6

Gene ID:
150771

Database links:

Entrez Gene: 150771 Human

Entrez Gene: 73338 Mouse

Entrez Gene: 499885 Rat

SwissProt: Q6GPH6 Human

SwissProt: A2ASA8 Mouse

SwissProt: Q66H52 Rat



產(chǎn)品圖片
Sample: Panc-1(Human) Cell Lysate at 30 ug Primary: Anti-ITPRIPL1 (bs-17187R) at 1/300 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 61 kD Observed band size: 61 kD
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
99在线中文字幕一区| 精品国产品国语在线不卡| 国产三级久久久久久久久久| 欧美一区二区三区成| 欧美日韩国产综合在线视频| 国产日韩欧美老人啪啪| 动漫无码AV在线免费观看| 一区二区三区四区欧美日韩亚洲| 国产r级亚洲r级在线观看| 精品久久久久久红码专区| 亚洲欧洲欧美中文日韩| 日韩精品一区二区三区在线| 久久久久久999一区二区三区| 亚洲国产午夜精品不卡| 欧美大片免费看片入口| 国产精品久久久久粉嫩小| 成人毛片女人18免费片| 久久久久久亚洲一区二区| 亚洲视频专区一区二区| 欧美老熟女多毛茸茸| 亚洲AV永久无码精品加勒比| 精品久久久久久久久久中文幕| 91香蕉频蕉app下载| 国产三级久久久久久久久久| 国产精品一区二区30p| 白嫩丰满少妇一区二区| 久久久久国产精品老熟女| 国产视频网站在线不卡| 国产欧美一区二区综合日本| 国产激情老熟女一区二区| 欧美日本aⅴ一区二区三区| 亚洲AV综合色一区二区三区| 欧美中文亚洲国产日韩| 91精品国产综合久久久福利| 亚洲人妻最新中文AV| 国产精品不卡a∨在线观看| 国产美女高潮抽搐流水在线看| 精品无码中文字幕在线| 经典国产乱子伦精品| 亚洲精品夜夜夜妓女网| 国产精品毛片大码女人|