Explore
Validate
Learn
Western blotAntibody data
- Antibody Data
- Antigen structure
- References [0]
- Comments [0]
- Validations
- Western blot [2]
- Immunohistochemistry [2]
Submit
Validation data
Reference
Comment
Report error
- Product number
- PA1-41633 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- XPO4 Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide
- Description
- PA1-41633 detects Exportin-4 in chicken, chimpanzee, rhesus monkey, canine, human, rat and mouse samples.
- Concentration
- 0.5 mg/mL
No comments: Submit comment
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis ofExportin-4 inJurkatcelllysate in the 1) absence and 2) presence of immunizing peptide using a Exportin 4 polyclonal antibody (Product # PA1-41633) at2 µg/mL.
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis of XPO4 in Jurkat cell lysate in the 1) absence and 2) presence of immunizing peptide. Samples were incubated in XPO4 polyclonal antibody (Product # PA1-41633).
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunohistochemical analysis of XPO4 in formalin-fixed, paraffin-embedded human hepatocellular carcinoma. Samples were incubated in XPO4 polyclonal antibody (Product # PA1-41633) using a dilution of 5 µg/mL followed by peroxidase-conjugate and DAB chromogen. Staining of formalin-fixed tissues is enhanced by boiling tissue sections in 10 mM sodium citrate buffer, pH 6.0 for 10-20 min followed by cooling at RT for 20 min.
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunohistochemical analysis of XPO4 in formalin-fixed, paraffin-embedded human liver. Samples were incubated in XPO4 polyclonal antibody (Product # PA1-41633) using a dilution of 5 µg/mL followed by peroxidase-conjugate and DAB chromogen. Staining of formalin-fixed tissues is enhanced by boiling tissue sections in 10 mM sodium citrate buffer, pH 6.0 for 10-20 min followed by cooling at RT for 20 min.
