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OTX2 Monoclonal Antibody

商品貨號： PLA004967

適應(yīng) 性： 人

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說明書

商品描述

發(fā)貨日期： 7
基因名稱： OTX2
蛋白名稱： Homeobox protein OTX2
Human_gene_id： 5015
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5015
Human_swiss_prot_no： P32243
Human_swiss_link： http://www.uniprot.org/uniprotkb/P32243/entry
Mouse_swiss_prot_no： P80206
Mouse_swiss_link： http://www.uniprot.org/uniprot/P80206
特異性： OTX2 Monoclonal Antibody detects endogenous levels of OTX2 protein.
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Monoclonal, Mouse
稀釋： WB 1:500 - 1:2000. IHC 1:200 - 1:1000. IF 1:200 - 1:1000. Flow cytometry: 1:200 - 1:400. ELISA: 1:10000. Not yet tested in other applications.
純化工藝： Affinity purification
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： OTX2; Homeobox protein OTX2; Orthodenticle homolog 2
功能： developmental stage:Embryo.,disease:Defects in OTX2 are the cause of microphthalmia syndromic type 5 (MCOPS5) [MIM:610125]. Microphthalmia is a clinically heterogeneous disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues. Up to 80% of cases of microphthalia occur in association with syndromes that include non-ocular abnormalities. MCOPS5 patients manifest unilateral or bilateral microphthalmia/clinical anophthalmia and variable additional features including coloboma, microcornea, cataract, retinal dystrophy, hypoplasia or agenesis of the optic nerve, agenesis of the corpus callosum, developmental delay, joint laxity, hypotonia, and seizures.,function:Probably plays a role in the development of the brain and the sense organs. Can bind to the BCD target sequence (BTS): 5'-TCTAATCCC-3'.,similarity:Belongs to the paired homeobox family. Bicoid subfamily.,similarity:Contains 1 homeobox DNA-binding domain.,tissue specificity:Expressed in brain.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Nucleus .
組織表達(dá)： Eye,Retina,
科研貨號： PLA004967

OTX2 Monoclonal Antibody

Catalog No PLA004967

Product information

發(fā)貨日期： 7
基因名稱： OTX2
蛋白名稱： Homeobox protein OTX2
Human_gene_id： 5015
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5015
Human_swiss_prot_no： P32243
Human_swiss_link： http://www.uniprot.org/uniprotkb/P32243/entry
Mouse_swiss_prot_no： P80206
Mouse_swiss_link： http://www.uniprot.org/uniprot/P80206
特異性： OTX2 Monoclonal Antibody detects endogenous levels of OTX2 protein.
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Monoclonal, Mouse
稀釋： WB 1:500 - 1:2000. IHC 1:200 - 1:1000. IF 1:200 - 1:1000. Flow cytometry: 1:200 - 1:400. ELISA: 1:10000. Not yet tested in other applications.
純化工藝： Affinity purification
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： OTX2; Homeobox protein OTX2; Orthodenticle homolog 2
功能： developmental stage:Embryo.,disease:Defects in OTX2 are the cause of microphthalmia syndromic type 5 (MCOPS5) [MIM:610125]. Microphthalmia is a clinically heterogeneous disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues. Up to 80% of cases of microphthalia occur in association with syndromes that include non-ocular abnormalities. MCOPS5 patients manifest unilateral or bilateral microphthalmia/clinical anophthalmia and variable additional features including coloboma, microcornea, cataract, retinal dystrophy, hypoplasia or agenesis of the optic nerve, agenesis of the corpus callosum, developmental delay, joint laxity, hypotonia, and seizures.,function:Probably plays a role in the development of the brain and the sense organs. Can bind to the BCD target sequence (BTS): 5'-TCTAATCCC-3'.,similarity:Belongs to the paired homeobox family. Bicoid subfamily.,similarity:Contains 1 homeobox DNA-binding domain.,tissue specificity:Expressed in brain.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Nucleus .
組織表達(dá)： Eye,Retina,
科研貨號： PLA004967

Hunan UPT Biotechnology Co.,Ltd

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E-mail：service@uptbio.com

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