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
一区二区三区有码在线播放,国产一区二区久久久久久久免费,精品一区二区三区av
首頁 > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
Rabbit Anti-RBED1  antibody (bs-21284R)  
~~~促銷代碼KT202411~~~
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: 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-21284R
英文名稱 Rabbit Anti-RBED1  antibody
中文名稱 RNA結(jié)合蛋白RBED1抗體
別    名 C330008I15Rik; ELMO domain containing protein 3; ELMOD 3; ELMOD3; FLJ21977; FLJ35601; MGC111036; RBED 1; RBM 29; RBM29; RNA binding motif and ELMO domain 1; RNA binding motif and ELMO domain containing protein 1; RNA binding motif and ELMO/CED 12 domain 1; RNA binding motif protein 29; RNA binding protein 29.  
研究領(lǐng)域 細胞生物  細胞凋亡  結(jié)合蛋白  G蛋白信號  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human)
產(chǎn)品應(yīng)用 IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 43kDa
細胞定位 細胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human RBED1: 301-381/381 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 Preservative: 0.02% Proclin300, Constituents: 1% BSA, 0.01M PBS, pH7.4.
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 RBED1 (RNA binding motif and ELMO domain 1) contains an ELMO domain. There are 6 named isoforms produced by alternative splicing.

Function:
Acts as a GTPase-activating protein (GAP) for ARL2 with low specific activity.

Subunit:
Contains 1 ELMO domain.

Tissue Specificity:
Both isoform 1 and isoform 6 are widely expressed.

DISEASE:
The disease is caused by mutations affecting the gene represented in this entry. Disease description:A form of non-syndromic deafness characterized by prelingual onset of severe to profound mixed conductive and sensorineural hearing loss.

SWISS:
Q96FG2

Gene ID:
84173

Database links:

Entrez Gene: 84173 Human

SwissProt: Q96FG2 Human

Unigene: 269990 Human



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
漳平市| 高密市| 连江县| 闽清县| 宁强县| 赫章县| 乐亭县| 贵南县| 牙克石市| 喀什市| 潮州市| 九江县| 海伦市| 茂名市| 崇阳县| 巴彦淖尔市| 阳新县| 胶南市| 天柱县| 体育| 金湖县| 九江县| 富裕县| 香河县| 潍坊市| 新蔡县| 定远县| 华安县| 从化市| 阿克苏市| 稷山县| 桃源县| 吉隆县| 平江县| 山东省| 桐梓县| 山阳县| 铜陵市| 龙江县| 吴堡县| 油尖旺区|