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Product Name
FOXP3 Mouse (7H9) mAb
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Gene ID
50943
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SwissProt ID
Q9BZS1
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Gene Name
FOXP3
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Alternative Names
FOXP3; IPEX; JM2; Forkhead box protein P3; Scurfin
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Background
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.
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Research Field
Cell Biology
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Product Categories
Primary antibody
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Host
Mouse
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Reactivity
Transfected
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Application
WB,ICC/IF
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Dilution Ratio
WB: 1/500-1/1000 IF: 1/50-1/200
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Molecular Weight
Calculated MW: 47 kDa; Observed MW: 47 kDa
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Clonality
Monoclonal Antibody
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Clonality No.
7H9-D6-A10
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Isotype
IgG1
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Immunogen
Purified recombinant human FOXP3 protein fragments expressed in E.coli.
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Purification
Affinity Purified
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Conjugation
Unconjugated
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Modification
Unmodified
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Form
Liquid
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Buffer System
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide, pH 7.3.
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Storage
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.