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FoxP3 Monoclonal Antibody

商品貨號： PLA004816

適應性： 人,小鼠

￥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： FOXP3
蛋白名稱： Forkhead box protein P3
Human_gene_id： 50943
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=50943
Human_swiss_prot_no： Q9BZS1
Human_swiss_link： http://www.uniprot.org/uniprotkb/Q9BZS1/entry
Mouse_gene_id： 20371
Mouse_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=20371
Mouse_swiss_prot_no： Q99JB6
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q99JB6
特異性： FoxP3 Monoclonal Antibody detects endogenous levels of FoxP3 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. ELISA: 1:10000. Not yet tested in other applications.
純化工藝： Affinity purification
濃度： 1 mg/ml
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： FOXP3; IPEX; JM2; Forkhead box protein P3; Scurfin
功能： disease:Defects in FOXP3 are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) [MIM:304790]; also known as X-linked autoimmunity-immunodeficiency syndrome. IPEX is characterized by neonatal onset insulin-dependent diabetes mellitus, infections, secretory diarrhea, trombocytopenia, anemia and eczema. It is usually lethal in infancy.,function:Probable transcription factor. Plays a critical role in the control of immune response.,online information:FOXP3 entry,online information:FOXP3 mutation db,similarity:Contains 1 C2H2-type zinc finger.,similarity:Contains 1 fork-head DNA-binding domain.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細胞定位： Nucleus . Cytoplasm . Predominantly expressed in the cytoplasm in activated conventional T-cells whereas predominantly expressed in the nucleus in regulatory T-cells (Treg). The 41 kDa form derived by proteolytic processing is found exclusively in the chromatin fraction of activated Treg cells (By similarity). .
科研貨號： PLA004816

FoxP3 Monoclonal Antibody

Catalog No PLA004816

Product information

發(fā)貨日期： 7
基因名稱： FOXP3
蛋白名稱： Forkhead box protein P3
Human_gene_id： 50943
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=50943
Human_swiss_prot_no： Q9BZS1
Human_swiss_link： http://www.uniprot.org/uniprotkb/Q9BZS1/entry
Mouse_gene_id： 20371
Mouse_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=20371
Mouse_swiss_prot_no： Q99JB6
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q99JB6
特異性： FoxP3 Monoclonal Antibody detects endogenous levels of FoxP3 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. ELISA: 1:10000. Not yet tested in other applications.
純化工藝： Affinity purification
濃度： 1 mg/ml
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： FOXP3; IPEX; JM2; Forkhead box protein P3; Scurfin
功能： disease:Defects in FOXP3 are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) [MIM:304790]; also known as X-linked autoimmunity-immunodeficiency syndrome. IPEX is characterized by neonatal onset insulin-dependent diabetes mellitus, infections, secretory diarrhea, trombocytopenia, anemia and eczema. It is usually lethal in infancy.,function:Probable transcription factor. Plays a critical role in the control of immune response.,online information:FOXP3 entry,online information:FOXP3 mutation db,similarity:Contains 1 C2H2-type zinc finger.,similarity:Contains 1 fork-head DNA-binding domain.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細胞定位： Nucleus . Cytoplasm . Predominantly expressed in the cytoplasm in activated conventional T-cells whereas predominantly expressed in the nucleus in regulatory T-cells (Treg). The 41 kDa form derived by proteolytic processing is found exclusively in the chromatin fraction of activated Treg cells (By similarity). .
科研貨號： PLA004816

Hunan UPT Biotechnology Co.,Ltd

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