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
精品久久久久免费视,欧美亚洲免费高清在线观看,村上凉子一区二区三区
Rabbit Anti-ITPRIPL1/PE Conjugated antibody (bs-17187R-PE)
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: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-17187R-PE
英文名稱1 Rabbit Anti-ITPRIPL1/PE Conjugated antibody
中文名稱 PE標(biāo)記的ITPRIPL1蛋白抗體
別    名 Inositol 1,4,5 triphosphate receptor interacting protein like 1; IPIL1; KIAA1754 like; KIAA1754L.  
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  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, Dog, Cow, Horse, 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 61kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ITPRIPL1
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 癈 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癈. 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 癈.
產(chǎn)品介紹 background:
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.

Database links:

Entrez Gene: 150771 Human

Entrez Gene: 73338 Mouse

Entrez Gene: 499885 Rat

SwissProt: Q6GPH6 Human

SwissProt: A2ASA8 Mouse

SwissProt: Q66H52 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.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
人人爽人人爽人人妻av| 国产成人亚洲综合91精品首页| 亚洲国产精品久久久久麻| 久久久成人国产精品麻豆| 日韩精品高清在线观看| 国产精品久久久久久久久久一区| 一区二区三区欧美日本| 国产麻豆精品三级在线播放| 欧美日本aⅴ一区二区三区| 美女久久久高潮喷水91| 国产精品日韩在线亚洲一区| 亚洲国产精品久久久久网站| 国产在线观看污污污网站| 欧美黑粗大长在线不卡| 国产v亚洲v天堂无码| 亚洲国产精品久久久久网站| 亚洲91精品视频在线观看| 久久精品亚洲成在人线av| 欧美黄片一区二区免费| 亚洲欧美日韩国产精品专区| 亚洲国产精品一区二区三区久久| 男人的天堂黄色大片| 亚洲高清日韩中文字幕| 亚洲国产精品午夜福利久久| 日韩一区二区三区射精合集| 国产黄在线视频免费| 日韩一区二区三区在线观看视频| 极品少妇欧美一区二区| 国产精品国语对白在线观看| 97久久人人超碰国产精品| 久久久久久999一区二区三区| 日本欧美一区二区免费不卡| 亚洲欧美在线观看视频| 95精品视频在线观看| 国产精品一区二区久久| 久久国产无码模特视频| 人妻少妇精品无码专区漫画| 久久国产亚洲一区二区三区| 久久久久无码精品国产app| 亚洲av无码网站yw尤物| 日本一区二区三区影院|