FOXN1 Polyclonal Antibody

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商品货号： PLA005944

适应性： 人,大鼠,小鼠,

￥600元

规格：

40μL 100μL 200μL

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说明书

商品描述

基因名称： FOXN1 RONU WHN
蛋白名称： Forkhead box protein N1 (Winged-helix transcription factor nude)
Human_gene_id： 8456
Human_swiss_prot_no： O15353
Human_swiss_link： https://www.uniprot.org/uniprotkb/O15353/entry
Mouse_swiss_prot_no： Q61575
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q61575
特异性： FOXN1 Polyclonal Antibody detects endogenous levels of protein.
组成： Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： WB 1:500-2000 ELISA 1:5000-20000
纯化工艺： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度： 1 mg/ml
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
实测条带： 71kD
功能： disease:Defects in FOXN1 are the cause of T-cell immunodeficiency congenital alopecia and nail dystrophy [MIM:601705].,function:Transcriptional regulator involved in development.,online information:FOXN1 mutation db,similarity:Contains 1 fork-head DNA-binding domain.,tissue specificity:Expressed in thymus.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Nucleus.
组织表达： Expressed in thymus.
科研货号： PLA005944

FOXN1 Polyclonal Antibody

Catalog No PLA005944

Product information

基因名称： FOXN1 RONU WHN
蛋白名称： Forkhead box protein N1 (Winged-helix transcription factor nude)
Human_gene_id： 8456
Human_swiss_prot_no： O15353
Human_swiss_link： https://www.uniprot.org/uniprotkb/O15353/entry
Mouse_swiss_prot_no： Q61575
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q61575
特异性： FOXN1 Polyclonal Antibody detects endogenous levels of protein.
组成： Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： WB 1:500-2000 ELISA 1:5000-20000
纯化工艺： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度： 1 mg/ml
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
实测条带： 71kD
功能： disease:Defects in FOXN1 are the cause of T-cell immunodeficiency congenital alopecia and nail dystrophy [MIM:601705].,function:Transcriptional regulator involved in development.,online information:FOXN1 mutation db,similarity:Contains 1 fork-head DNA-binding domain.,tissue specificity:Expressed in thymus.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Nucleus.
组织表达： Expressed in thymus.
科研货号： PLA005944

Hunan UPT Biotechnology Co.,Ltd

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