Application
Phospho-mPLM-pS83 western blot analysis in mouse kidney tissue lysates (35ug/lane).This demonstrates the Plm antibody detected the Plm protein (arrow).Application
Dot blot analysis of anti-Phospho-mPLM-pS83 Phospho-specific Pab on nitrocellulose membrane. 50ng of Phospho-peptide or Non Phospho-peptide per dot were adsorbed. Antibody working concentrations are 0.6ug per ml.| Product Name | Phospho-PLM-S83 Antibody |
|---|---|
| Antibody Type | Primary Antibodies |
| Modification | p-S83 |
| Clonality | Polyclonal |
|---|---|
| Isotype | Ig |
| Host Species | Rabbit |
| Tested Applications | WBDB |
| WB:1:100~500 DB |
|
| Species Reactivity | Human |
| Concentration | 1mg/ml |
| Gene Synonyms | Plm |
|---|---|
| Alternative Names | Fxyd1 Plm Phospholemman FXYD domain-containing ion transport regulator 1 |
| Molecular Weight(MW) | 10323 Da |
| Function | May have a functional role in muscle contraction. Induces a hyperpolarization-activated chloride current when exogenously expressed (By similarity) |
| Tissue Specificity | This Mouse Phospho-PLM-S83 antibody is generated from rabbits immunized with a KLH conjugated synthetic phosphopeptide between 63~92 amino acids from the C-terminal region of mouse PLM. |
| Cellular Localization | Membrane; Single-pass type I membrane protein |
| Entrez Gene | 56188 |
|---|
Application
Phospho-mPLM-pS83 western blot analysis in mouse kidney tissue lysates (35ug/lane).This demonstrates the Plm antibody detected the Plm protein (arrow).
Application
Dot blot analysis of anti-Phospho-mPLM-pS83 Phospho-specific Pab on nitrocellulose membrane. 50ng of Phospho-peptide or Non Phospho-peptide per dot were adsorbed. Antibody working concentrations are 0.6ug per ml.| Application Notes | WB:1:100~500 DB |
|---|
| 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 first purified by protein G affinity chromatography. Then, the antibody fraction is peptide affinity purified in a 2-step procedure with control and phosphorylated peptides. The phospho-specific antibody is eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS. |
