Phosphoserine (incl. pos. control) Mouse Monoclonal Antibody [Clone ID: 16B4]
$620.00
2 Weeks*
Specifications
| Product Data | |
| Clone Name | 16B4 |
|---|---|
| Application | ELISA, IP, WB |
| Recommended Dilution | Included Positive control: pSer / pThr Molecular Weight Marker Formulation: The pSer/pThr molecular weight marker contains rabbit muscle phosphoproteins isolated by Fe3+/IDA - affinity chromatography. Proteins are lyophilized from PBS/NaF/PEG/Sucrose/ Bromophenolblue and Na - azide. After reconstitution the solution contains 0.09% Na-azide. Stability: Reconstitute by addition of 200 µl H2O. After complete solubilization add 200 µl 2x SDS-PAGE sample buffer, mix and incubate at 90°C for 5 min. Application: The pSer/pThr molecular weight marker is recommended for immunoblot applications. Use 20µl molecular weight marker per lane. Note: Use BSA based blot incubation buffers. Milk, Casein and Blotto might interfere with antibody - antigen interaction. Storage: Aliquote and store frozen. Avoid repeated freeze/thaw cycles. Shelf life: one year from despatch. |
| Reactivity | Canine, Human, Mouse, Rat |
| Antibody Host | Mouse |
| Isotype | IgM |
| Clonality | Monoclonal |
| Immunogen | Phosphopeptide conjugated to KLH. |
| Specificity | AM00117PU-N recognizes a broad range of serine-phosphorylated proteins in crude cell extracts, preferring positively charged amino acids directly neighboured to phosphoserine. |
| Buffer | 1 ml 2x PBS containing 0.09% Sodium Azide, PEG and Sucrose State: Purified State: Lyophilized purified Ig fraction |
| Reconstitution Method | Restore with 1.0 ml H2O (15 min, RT). |
| Purification | Size Exclusion Chromatography. |
| Conjugation | Unconjugated |
| Storage | Store lyophilized (preferably in a desiccator) at -20°C and reconstituted (aliquote and freeze in liquid nitrogen) at -80°C. Avoid repeated freezing and thawing. Thaw aliquots at 37°C. Thawed aliquots may be stored at 4°C up to 1 week. |
| Stability | Shelf life: one year from despatch. |
| Shipping | Ambient |
| Background | Phosphorylation and dephosphorylation of cellular proteins are central steps in transducing extracellular signals to the cell nucleus. Phosphorylated epitopes may serve as docking sites for the assembly of protein complexes or may alter the 3-dimensional protein structure thus modulating enzymatic activity or the ability to undergo protein-protein-interactions. Modification of proteins on serine residues is mediated by serine/threonine kinases. Please note that phosphoserine detection by monoclonal antibodies is always dependent on the surrounding amino acid sequence! |
| Reference Data | |
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*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen
complexities in the preparation of your product. International customers may expect an additional 1-2 weeks
in shipping.