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(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: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
中文字幕一区二区久久,欧美精品日韩一区二区,综合网日日天干夜夜久久
Rabbit Anti-ITPRIPL1/Gold Conjugated antibody (bs-17187R-Gold)
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@m.p2b3.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@m.p2b3.cn
說(shuō) 明 書(shū): 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢(xún)價(jià)
產(chǎn)品編號(hào) bs-17187R-Gold
英文名稱(chēng)1 Rabbit Anti-ITPRIPL1/Gold Conjugated antibody
中文名稱(chēng) 膠體金標(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(jià)格 100ul/2980元 購(gòu)買(mǎi)        大包裝/詢(xún)價(jià)
說(shuō) 明 書(shū) 100ul(10nm  15nm  35nm
研究領(lǐng)域 細(xì)胞生物  免疫學(xué)  通道蛋白  
抗體來(lái)源 Rabbit
克隆類(lèi)型 Polyclonal
交叉反應(yīng) Human, Mouse,  (predicted: Rat, Dog, Cow, Horse, Sheep, )
產(chǎn)品應(yīng)用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
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 0.4mg/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(chǔ) 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
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(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)
动漫无码AV在线免费观看| 欧美日韩国产精品视频一区| 国语自产精品视频二区在线| 亚洲av乱码一区二区三区女| 欧美日韩永久精品一区二区| 99久久精品国产一区二区三区?| 91久久久久久久国产| 国内自拍2019在线| 亚洲综合激情另类小说区| 国产在线观看一区视频| 国产精品国语对白在线观看| 成人午夜日韩看片后入| 女人之爱女同电影中文字幕| 国产成人欧美日本在线观看| 日韩精品一区二区av蜜桃| 国产三级免费在线播放| 高清国产午夜精品久久久久久| 久久精品成人免费国产| 中文字幕无码aⅴ免费不卡| 亚洲日韩欧美制服第一页| 国内精品国产三级国产av万事达| 欧美乱码精品一区二区三区卡| 亚洲综合精品欧美日韩一区二区三区91| 九色九九综合久久爱| 中文字幕字幕一区二区三区| 成人精品黄色一二三区| 久久久久久999一区二区三区| 国产精品一区二区97| 日韩在线|中文字幕| 国产精品日本一区二区在线看| 国产微拍无码精品一区| 丰满少妇人妻久久久久久| 亚洲一道本中文字幕一区二区| 国产精品亚洲一区二区三区欲| 欧美一级黄片在线播放| 国产一级二级三级精品| 国产av福利第一精品| 国产精品18禁久久久久久久久| 日韩精品中文字幕欧美| 88国产精品视频一区二区三区| 精品国产品国语在线不卡|