日日操日日操,亚洲一区二区三区四区视频,成人午夜福利激情,无码中文7幕

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  關(guān)于我們  聯(lián)系我們
亚州精品福利,嗯啊不要一区中文字幕,综合成人超碰在线
首頁 > 產(chǎn)品中心 > 一抗 > 產(chǎn)品信息
SFT2B Rabbit pAb (bs-17304R)  
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價
產(chǎn)品編號 bs-17304R
英文名稱 SFT2B Rabbit pAb
中文名稱 囊泡轉(zhuǎn)運蛋白SFT2B抗體
別    名 FLJ34085; SFT2 domain containing 2; SFT2 domain-containing protein 2; SFT2B_HUMAN; Sft2d2; UNQ512; Vesicle transport protein SFT2B.  
研究領(lǐng)域 腫瘤  細(xì)胞生物  免疫學(xué)  神經(jīng)生物學(xué)  轉(zhuǎn)運蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應(yīng) (predicted: Human,Mouse,Rat,Rabbit,Sheep)
產(chǎn)品應(yīng)用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 18 kDa
檢測分子量
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 SFT2B: 1-100/160 <Cytoplasmic>
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 SFT2D2 is a 160 amino acid multi-pass membrane protein that belongs to the SFT2 family. SFT2D2 may be involved in fusion of retrograde transport vesicles derived from an endocytic compartment with the Golgi complex. The SFT2D2 gene is conserved in dog, cow, mouse, rat, chicken, A.thaliana and rice, and maps to human chromosome 1q24.2. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

Function:
May be involved in fusion of retrograde transport vesicles derived from an endocytic compartment with the Golgi complex.

Subcellular Location:
Membrane.

Similarity:
Belongs to the SFT2 family.

SWISS:
O95562

Gene ID:
375035

Database links:

Entrez Gene: 375035 Human

Entrez Gene: 108735 Mouse

Entrez Gene: 360868 Rat

SwissProt: O95562 Human

SwissProt: Q8VD57 Mouse

SwissProt: Q4FZV2 Rat

Unigene: 645435 Human

Unigene: 288369 Mouse

Unigene: 8424 Rat



版權(quán)所有 2004-2026 bklrv.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
日韩国产色图一区二区| 九九归一一区二区三区| 伊人春色一区二区三区久久| 九九网友自拍| 精品久久老司机视频| 97se国产欧美日韩| 日韩精品成人中文字幕| 青青草原成人在线最新| 精品国产日韩欧美一区二区| 婷婷五月四色91在线成人网| 最新99re在线观看| 国产H片一区二区| 中山av影音资源网| 久久婷婷色综合一区二区三区| 色花堂在线观看一区二区三区| 伦理久久久| 欧美日逼欢看| 久久久久久香蕉| 草青青av免费| 看黄色三级射精片| 久久少妇系列| 亚洲成人77777在线播放| 国产伦精品一区二区三区不卡网| 色呦呦中文免费观看| 麻豆综合精品| 香蕉大奶在线| 高清中文字幕 av 三区| 人人有妻 一区二区 三区| 性做久久久久久久不卡| 放一个操逼的看一下| 久久亚洲高潮免费视频| 国产美欧弟二页| 欧美熟妇夜夜爽| 国际午夜理论精品| 亚洲日韩一区二区中文字幕 | 国产乱人伦精品一区在线观看| 麻豆AV影院| 国产精品性淫乱视频网站| 无码一区免费网站| 日韩一级黄片一区二区三区在线观看 | 韩日人妻中文字幕一区二区|