Antibody data
- Antibody Data
- Antigen structure
- References [0]
- Comments [0]
- Validations
- Western blot [1]
- Immunohistochemistry [3]
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Validation data
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- Product number
- LS-C408072 - Provider product page
- Provider
- LSBio
- Product name
- DIABLO / SMAC Antibody (aa56-239) LS-C408072
- Antibody type
- Polyclonal
- Description
- Immunogen affinity purified
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Storage
- At -20°C for 1 year. After reconstitution, at 4°C for 1 month. It can also be aliquotted and stored frozen at -20°C for a longer time. Avoid freeze-thaw cycles.
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Supportive validation
- Submitted by
- LSBio (provider)
- Enhanced method
- Genetic validation
- Main image
- Experimental details
- Western blot analysis of Smac/Diablo expression in rat testis extract (lane 1), 22RV1 whole cell lysates (lane 2) and SKOV whole cell lysates (lane 3). Smac/Diablo at 25 kD was detected using rabbit anti- Smac/Diablo Antigen Affinity purified polyclonal antibody at 0.5 ug/mL. The blot was developed using chemiluminescence (ECL) method.
Supportive validation
- Submitted by
- LSBio (provider)
- Enhanced method
- Genetic validation
- Main image
- Experimental details
- Smac/Diablo was detected in paraffin-embedded sections of mouse testis tissues using rabbit anti- Smac/Diablo Antigen Affinity purified polyclonal antibody at 1 ug/mL. The immunohistochemical section was developed using SABC method.
- Submitted by
- LSBio (provider)
- Enhanced method
- Genetic validation
- Main image
- Experimental details
- Smac/Diablo was detected in paraffin-embedded sections of rat testis tissues using rabbit anti- Smac/Diablo Antigen Affinity purified polyclonal antibody at 1 ug/mL. The immunohistochemical section was developed using SABC method.
- Submitted by
- LSBio (provider)
- Enhanced method
- Genetic validation
- Main image
- Experimental details
- Smac/Diablo was detected in paraffin-embedded sections of human testis tissues using rabbit anti- Smac/Diablo Antigen Affinity purified polyclonal antibody at 1 ug/mL. The immunohistochemical section was developed using SABC method.