Application
BMP2 Antibody (Center) western blot analysis in CEM cell line lysates (35ug/lane).This demonstrates the BMP2 antibody detected the BMP2 protein (arrow).Application
BMP2 Antibody (Center) flow cytometric analysis of Hela cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.| Product Name | BMP2 Antibody (Center) |
|---|---|
| Antibody Type | Primary Antibodies |
| Antigen Alias | BMP2; BMP2A; Bone morphogenetic protein 2; Bone morphogenetic protein 2A |
| Clonality | Polyclonal |
|---|---|
| Isotype | Ig |
| Host Species | Rabbit |
| Tested Applications | WBFC |
| WB:1:100~500 FC |
|
| Species Reactivity | Human |
| Concentration | 1mg/ml |
| Gene Synonyms | BMP2A |
|---|---|
| Alternative Names | BMP2 BMP2A Bone morphogenetic protein 2 Bone morphogenetic protein 2A |
| Molecular Weight(MW) | 44702 Da |
| Function | Induces cartilage and bone formation. |
| Tissue Specificity | Particularly abundant in lung, spleen and colon and in low but significant levels in heart, brain, placenta, liver, skeletal muscle, kidney, pancreas, prostate, ovary and small intestine |
| Cellular Localization | Secreted. |
| Entrez Gene | 650 |
|---|---|
| Nucleotide Accession | NP_001191.1 |
Application
BMP2 Antibody (Center) western blot analysis in CEM cell line lysates (35ug/lane).This demonstrates the BMP2 antibody detected the BMP2 protein (arrow).
Application
BMP2 Antibody (Center) flow cytometric analysis of Hela cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.| Application Notes | WB:1:100~500 FC |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles. |
| Storage Buffer | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
