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SOX9 Rabbit mAb

商品貨號(hào)： PRM8547

適應(yīng) 性： Human,Mouse,Rat,

￥800元

規(guī)格：

50ul

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說明書

商品描述

發(fā)貨日期：現(xiàn)貨
靶點(diǎn)-Target： Sox-9
反應(yīng)性-Reactivity： Human,Mouse,Rat,
應(yīng)用-Applications： WB,IHC,IF,ELISA
MW(Calculated)： 56kD
MW(Observed)： 70kD
宿主物種-Host Species： Rabbit
同種型-Isotype： IgG,Kappa
偶聯(lián)-Conjugate： Unmodified
推薦稀釋比： IHC 1:200-1:1000;WB 1:500-1:1000;IF 1:200-1:1000;ELISA 1:5000-1:20000
組成： PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
純化工藝： Protein A
儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆號(hào)： PT0295R
特異性： Endogenous
基因名稱： SOX9
蛋白名稱： Transcription factor SOX-9
Organism-1： Human
基因ID-1： 6662
SwissProt-1： P48436
背景： SRY-box 9(SOX9) Homo sapiens The protein encoded by this gene recognizes the sequence CCTTGAG along with other members of the HMG-box class DNA-binding proteins. It acts during chondrocyte differentiation and, with steroidogenic factor 1, regulates transcription of the anti-Muellerian hormone (AMH) gene. Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia, frequently with sex reversal. [provided by RefSeq, Jul 2008],
細(xì)胞定位： Nucleus

SOX9 Rabbit mAb

Catalog No PRM8547

Product information

發(fā)貨日期：現(xiàn)貨
靶點(diǎn)-Target： Sox-9
反應(yīng)性-Reactivity： Human,Mouse,Rat,
應(yīng)用-Applications： WB,IHC,IF,ELISA
MW(Calculated)： 56kD
MW(Observed)： 70kD
宿主物種-Host Species： Rabbit
同種型-Isotype： IgG,Kappa
偶聯(lián)-Conjugate： Unmodified
推薦稀釋比： IHC 1:200-1:1000;WB 1:500-1:1000;IF 1:200-1:1000;ELISA 1:5000-1:20000
組成： PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
純化工藝： Protein A
儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆號(hào)： PT0295R
特異性： Endogenous
基因名稱： SOX9
蛋白名稱： Transcription factor SOX-9
Organism-1： Human
基因ID-1： 6662
SwissProt-1： P48436
背景： SRY-box 9(SOX9) Homo sapiens The protein encoded by this gene recognizes the sequence CCTTGAG along with other members of the HMG-box class DNA-binding proteins. It acts during chondrocyte differentiation and, with steroidogenic factor 1, regulates transcription of the anti-Muellerian hormone (AMH) gene. Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia, frequently with sex reversal. [provided by RefSeq, Jul 2008],
細(xì)胞定位： Nucleus

Hunan UPT Biotechnology Co.,Ltd

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