SATB2 Rabbit mAb

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SATB2 Rabbit mAb

商品货号： PRM8026

适应性： 人,小鼠,大鼠

￥800元

规格：

50ul

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说明书

商品描述

发货日期：现货
靶点-Target： SATB2
反应性-Reactivity：人,小鼠,大鼠
应用-Applications： WB,IHC,IF,IP,ELISA
MW(Calculated)： 83kD
MW(Observed)： 100kD
宿主物种-Host Species： Rabbit
同种型-Isotype： IgG,Kappa
偶联-Conjugate： Unmodified
推荐稀释比： IHC 1:100-1:1000;WB 1:2000-1:10000;IF 1:200-1:1000;ELISA 1:5000-1:20000;IP 1:50-1:200;
组成： PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
纯化工艺： Protein A
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆号： PT0065R
特异性： Endogenous
基因名称： SATB2 KIAA1034
蛋白名称： DNA-binding protein SATB2 (Special AT-rich sequence-binding protein 2)
Organism-1： Human
基因ID-1： 23314
SwissProt-1： Q9UPW6
Organism-2： Mouse
SwissProt-2： Q8VI24
背景： This gene encodes a DNA binding protein that specifically binds nuclear matrix attachment regions. The encoded protein is involved in transcription regulation and chromatin remodeling. Defects in this gene are associated with isolated cleft palate and mental retardation. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Feb 2010],
细胞定位： Nucleus matrix .

SATB2 Rabbit mAb

Catalog No PRM8026

Product information

发货日期：现货
靶点-Target： SATB2
反应性-Reactivity：人,小鼠,大鼠
应用-Applications： WB,IHC,IF,IP,ELISA
MW(Calculated)： 83kD
MW(Observed)： 100kD
宿主物种-Host Species： Rabbit
同种型-Isotype： IgG,Kappa
偶联-Conjugate： Unmodified
推荐稀释比： IHC 1:100-1:1000;WB 1:2000-1:10000;IF 1:200-1:1000;ELISA 1:5000-1:20000;IP 1:50-1:200;
组成： PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
纯化工艺： Protein A
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆号： PT0065R
特异性： Endogenous
基因名称： SATB2 KIAA1034
蛋白名称： DNA-binding protein SATB2 (Special AT-rich sequence-binding protein 2)
Organism-1： Human
基因ID-1： 23314
SwissProt-1： Q9UPW6
Organism-2： Mouse
SwissProt-2： Q8VI24
背景： This gene encodes a DNA binding protein that specifically binds nuclear matrix attachment regions. The encoded protein is involved in transcription regulation and chromatin remodeling. Defects in this gene are associated with isolated cleft palate and mental retardation. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Feb 2010],
细胞定位： Nucleus matrix .

Hunan UPT Biotechnology Co.,Ltd

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