日本456免费观看456,2020国产在线a不卡片,自拍偷自拍亚洲精品第3页,男女激情高潮免费体验区,yy6080午夜福利网站,九国AV最新导航网站

亚洲国产日韩不卡综合,明星ai换脸磁力资源种子搜索,成人性闻CCAV下载,欧美日本国产在线a小说v,亚洲欧洲综合一区二区三区,里中结衣av中文字幕

> > > >

KCTD7 Polyclonal Antibody

商品貨號(hào)： PLA019616

適應(yīng) 性： 人,小鼠,大鼠

￥600元

規(guī)格：

40μL 100μL 200μL

在線咨詢

MSDS

說(shuō)明書(shū)

商品描述

基因名稱(chēng)： KCTD7
蛋白名稱(chēng)： KCTD7
Human_gene_id： 154881
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=154881
Human_swiss_prot_no： Q96MP8
Human_swiss_link： http://www.uniprot.org/uniprotkb/Q96MP8/entry
Mouse_gene_id： 212919
Mouse_swiss_prot_no： Q8BJK1
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q8BJK1
特異性： This antibody detects endogenous levels of KCTD7
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來(lái)源： Polyclonal, Rabbit,IgG
稀釋?zhuān)? WB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
說(shuō)明書(shū)： 1
Msds： MSDS_Antibody.pdf
其他名稱(chēng)： BTB/POZ domain-containing protein KCTD7
實(shí)測(cè)條帶： 33kD
功能： disease:Defects in KCTD7 are the cause of progressive myoclonic epilepsy type 3 (EPM3) [MIM:611726]. EPM3 is an autosomal recessive, severe, progressive myoclonic epilepsy with early-onset. Multifocal myoclonic seizures begin between 16 and 24 months of age after normal initial development. Neurodegeneration and regression occur with seizure onset. Other features include mental retardation, dysarthria, truncal ataxia, and loss of fine finger movements. EEG shows slow dysrhythmia, multifocal and occasionally generalized epileptiform discharges.,similarity:Contains 1 BTB (POZ) domain.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Cell membrane. Cytoplasm, cytosol.
組織表達(dá)： Brain,
科研貨號(hào)： PLA019616

KCTD7 Polyclonal Antibody

Catalog No PLA019616

Product information

基因名稱(chēng)： KCTD7
蛋白名稱(chēng)： KCTD7
Human_gene_id： 154881
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=154881
Human_swiss_prot_no： Q96MP8
Human_swiss_link： http://www.uniprot.org/uniprotkb/Q96MP8/entry
Mouse_gene_id： 212919
Mouse_swiss_prot_no： Q8BJK1
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q8BJK1
特異性： This antibody detects endogenous levels of KCTD7
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來(lái)源： Polyclonal, Rabbit,IgG
稀釋?zhuān)? WB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
說(shuō)明書(shū)： 1
Msds： MSDS_Antibody.pdf
其他名稱(chēng)： BTB/POZ domain-containing protein KCTD7
實(shí)測(cè)條帶： 33kD
功能： disease:Defects in KCTD7 are the cause of progressive myoclonic epilepsy type 3 (EPM3) [MIM:611726]. EPM3 is an autosomal recessive, severe, progressive myoclonic epilepsy with early-onset. Multifocal myoclonic seizures begin between 16 and 24 months of age after normal initial development. Neurodegeneration and regression occur with seizure onset. Other features include mental retardation, dysarthria, truncal ataxia, and loss of fine finger movements. EEG shows slow dysrhythmia, multifocal and occasionally generalized epileptiform discharges.,similarity:Contains 1 BTB (POZ) domain.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Cell membrane. Cytoplasm, cytosol.
組織表達(dá)： Brain,
科研貨號(hào)： PLA019616

Hunan UPT Biotechnology Co.,Ltd

Website：m.tjdqdt.com Servive hotline :4006916686

E-mail：service@uptbio.com

Address：

Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.

亚洲国产日韩不卡综合,明星ai换脸磁力资源种子搜索,成人性闻CCAV下载,欧美日本国产在线a小说v,亚洲欧洲综合一区二区三区,里中结衣av中文字幕