The Phospho-Smad5-S465 Monoclonal Antibody (CABP1411) is a high-quality antibody developed for reliable detection and analysis of target proteins. The protein encoded by this gene is involved in the transforming growth factor beta signaling pathway that results in an inhibition of the proliferation of hematopoietic progenitor cells. The encoded protein is activated by bone morphogenetic proteins type 1 receptor kinase, and may be involved in cancer. Alternative splicing results in multiple transcript variants.
This antibody is validated for use in WB, ELISA applications and has demonstrated reactivity against Human, Mouse, Rat samples.
Product Name:
Phospho-Smad5-S465 Monoclonal Antibody
SKU:
CABP1411
Size:
100μL, 20μL
Reactivity:
Human, Mouse, Rat
Clone Number:
ARC59204
Conjugate:
Unconjugated
Immunogen:
Synthetic peptide. This information is considered to be commercially sensitive.
Tested Applications:
WBELISA
Recommended Dilution:
WB
1:1000 - 1:5000
ELISA
Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
Synonyms:
DWFC, JV5-1, MADH5, Phospho-Smad5-S465
Positive Sample:
NIH/3T3 treated with BMP4, C6 treated with TGFβ and MG132, HT-1080 treated with BMP2
Cellular Localization:
Cytoplasm, Nucleus.
Calculated MW:
52 kDa
Observed MW:
52 kDa/60 kDa
The protein encoded by this gene is involved in the transforming growth factor beta signaling pathway that results in an inhibition of the proliferation of hematopoietic progenitor cells. The encoded protein is activated by bone morphogenetic proteins type 1 receptor kinase, and may be involved in cancer. Alternative splicing results in multiple transcript variants.
Purification Method
Affinity purification
Gene ID
4090
Buffer Information
Store at -20℃. Avoid freeze / thaw cycles. Buffer: PBS containing 50% glycerol and 0.05% BSA, preserved with proclin300 or sodium azide, pH 7.3.
Western blot analysis of lysates from NIH/3T3 cells, using Phospho-Smad5-S465 Rabbit mAb (CABP1411) at 1:2000 dilution. NIH/3T3 cells were treated with BMP4(50ng/ml) at 37℃ for 6 hours. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution. Lysates/proteins: 25μg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (AbGn00020). Exposure time: 180s.
Western blot analysis of lysates from C6 cells using Phospho-Smad5-S465 Rabbit mAb (CABP1411) at 1:1000 dilution incubated overnight at 4℃. C6 cells were treated with TGFβ3 (10 ng/mL) and MG132 (10 μM) for 30 minutes after serum starvation. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution. Lysates/proteins: 30 μg per lane. Blocking buffer: 3 % nonfat dry milk in TBST. Detection: ECL Basic Kit (AbGn00020). Exposure time: 20 s.
