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Phospho-IκBα-S32 Rabbit Monoclonal Antibody

Cat Number: AB0707
Conjugate: Unconjugated
Size: 100 ug
Clone: ARC0147
Concentration: 1mg/ml
Host: Rabbit
Isotype: IgG
Immunogen: Synthetic peptide. This information is considered to be commercially sensitive.
Reactivity: Human,Mouse,Rat
Applications: WB 1:500 - 1:2000 ELISA Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
Molecular: 39kDa/
Purification: Affinity purification
Synonyms: IKBA; MAD-3; NFKBI; EDAID2; Phospho-IκBα-S32
Background:

This gene encodes a member of the NF-kappa-B inhibitor family, which contain multiple ankrin repeat domains. The encoded protein interacts with REL dimers to inhibit NF-kappa-B/REL complexes which are involved in inflammatory responses. The encoded protein moves between the cytoplasm and the nucleus via a nuclear localization signal and CRM1-mediated nuclear export. Mutations in this gene have been found in ectodermal dysplasia anhidrotic with T-cell immunodeficiency autosomal dominant disease.

Form: liquid
Buffer: PBS containing 50% glycerol and 0.05% BSA, preserved with proclin300 or sodium azide (as specified on the Certificate of Analysis), pH 7.3.
Storage: Store at -20℃. Avoid freeze / thaw cycles.
Western blot analysis of lysates from NIH/3T3 cells, using Phospho-IκBα-S32 Rabbit mAb (AP0707) at 1:1000 dilution. NIH/3T3 and C6 cells were treated with TNF-α (20 ng/mL) at 37℃ for 30 minutes. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25μg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL West Pico Plus. Exposure time: 120s.

Western blot analysis of lysates from NIH/3T3 cells, using Phospho-IκBα-S32 Rabbit mAb (AP0707) at 1:1000 dilution. NIH/3T3 and C6 cells were treated with TNF-α (20 ng/mL) at 37℃ for 30 minutes.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.
Lysates/proteins: 25μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL West Pico Plus.
Exposure time: 120s.

Western blot analysis of lysates from C6 cells using Phospho-IκBα-S32 Rabbit mAb (AP0707) at 1:1000 dilution (upper) or IκBα Rabbit mAb (A24909) at1:6000 dilution (lower) incubated overnight at 4℃. C6 cells were treated with Calyculin A (100 nM) at 37℃ for 30 minutes after serum-starvation overnight. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 30 μg per lane. Blocking buffer: 3 % nonfat dry milk in TBST. Detection: ECL West Pico Plus. Exposure time: 60s.

Western blot analysis of lysates from C6 cells using Phospho-IκBα-S32 Rabbit mAb (AP0707) at 1:1000 dilution (upper) or IκBα Rabbit mAb (A24909) at1:6000 dilution (lower) incubated overnight at 4℃. C6 cells were treated with Calyculin A (100 nM) at 37℃ for 30 minutes after serum-starvation overnight.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.
Lysates/proteins: 30 μg per lane.
Blocking buffer: 3 % nonfat dry milk in TBST.
Detection: ECL West Pico Plus.
Exposure time: 60s.