Ancell

anti-FOXP3 (human), mAb (ANCFX2D7)

Product Code:
 
ANC-333-020
Product Group:
 
Primary Antibodies
Supplier:
 
Ancell
Host Type:
 
Mouse
Antibody Isotype:
 
Mouse IgG1κ
Antibody Clonality:
 
Monoclonal
Antibody Clone:
 
ANCFX2D7
Regulatory Status:
 
RUO
Target Species:
 
Human
Applications:
  • Enzyme-Linked Immunosorbent Assay (ELISA)
  • Flow Cytometry
Shipping:
 
BLUE ICE
Storage:
 
+4°C
 

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ANC-333-020-100ug100 ug£243.00
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This product comes from: Switzerland.
Typical lead time: 10-14 working days.
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Further Information

Alternate Names/Synonyms:
Forkhead Box Protein P3; Scurfin; IPEX, JM2
EClass:
32160000
Form (Short):
liquid
Formulation:
50mM Sodium phosphate pH7.5, 100mM Potassium chloride, 150mM NaCl, 0.5mg/ml Gentamicin sulfate (as preservative).
Handling Advice:
Avoid freeze/thaw cycles.
Immunogen:
Recombinant human FOXP3.
Long Description:
Monoclonal Antibody. Recognizes human FOXP3. Isotype: Mouse IgG1kappa. Clone: ANCFX2D7. Applications: ELISA, FACS. 50mM Sodium phosphate pH7.5, 100mM Potassium chloride, 150mM NaCl, 0.5mg/ml Gentamicin sulfate (as preservative). FOXP3 is involved in immune system responses. It functions as the master regulator in the development and function of regulatory T cells. FOX proteins belong to the forkhead/winged-helix family of transcriptional regulators and are presumed to exert control via similar DNA binding interactions during transcription. Defects in FOXP3 are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX); 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.
Package Type:
Plastic Vial
Product Description:
FOXP3 is involved in immune system responses. It functions as the master regulator in the development and function of regulatory T cells. FOX proteins belong to the forkhead/winged-helix family of transcriptional regulators and are presumed to exert control via similar DNA binding interactions during transcription. Defects in FOXP3 are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX); 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.
Purity:
>95% (SDS-PAGE)
Specificity:
Recognizes human FOXP3.
Transportation:
Non-hazardous
UNSPSC Category:
Primary Antibodies
UNSPSC Number:
12352203
Use & Stability:
Stable for at least 1 year after receipt when stored at +4°C.