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Western blotAntibody data
- Antibody Data
- Antigen structure
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- Validations
- Western blot [2]
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- Product number
- AF3957 - Provider product page
- Provider
- Novus Biologicals
- Product name
- Goat Polyclonal VAP-1/AOC3 Antibody
- Antibody type
- Polyclonal
- Description
- Antigen Affinity-purified. Detects human VAP-1/AOC3 in direct ELISAs and Western blots. In direct ELISAs, approximately 50% cross-reactivity with recombinant mouse VAP-1 is observed.
- Reactivity
- Human
- Host
- Goat
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 100 ug
- Concentration
- LYOPH
- Storage
- Use a manual defrost freezer and avoid repeated freeze-thaw cycles. 12 months from date of receipt, -20 to -70 degreesC as supplied. 1 month, 2 to 8 degreesC under sterile conditions after reconstitution. 6 months, -20 to -70 degreesC under sterile conditions after reconstitution.
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Supportive validation
- Submitted by
- Novus Biologicals (provider)
- Main image
- Experimental details
- Detection of Human VAP-1/AOC3 by Simple Western<SUP abp="261">TM. Simple Western lane view shows lysates of human lung tissue and heart tissue, loaded at 0.2 mg/mL. A specific band was detected for VAP-1/AOC3 at approximately 123 kDa (as indicated) using 10 µg/mL of Goat Anti-Human VAP-1/AOC3 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF3957) followed by 1:50 dilution of HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # HAF109). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system.
- Submitted by
- Novus Biologicals (provider)
- Main image
- Experimental details
- Detection of Human VAP-1/AOC3 by Western Blot. Western blot shows lysates of human lung tissue, human kidney tissue, human liver tissue, and human heart tissue. PVDF membrane was probed with 1 µg/mL of Goat Anti-Human VAP-1/AOC3 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF3957) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # HAF019). A specific band was detected for VAP-1/AOC3 at approximately 95-100 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.
