ARG23897

anti-Phosphoserine / threonine antibody [M380A + M380B]

anti-Phosphoserine / threonine antibody [M380A + M380B] for ELISA,ICC/IF,Immunoprecipitation,Western blot and Other

Overview

Product Description Mouse Monoclonal antibody [M380A + M380B] recognizes Phosphoserine / threonine
Tested Reactivity Other
Tested Application ELISA, ICC/IF, IP, WB
Specificity This antibody detects many serine or threonine phosphorylated proteins by WB, ICC and ELISA. This product is a mix of two clones: M380A and M380B.
Host Mouse
Clonality Monoclonal
Clone M380A + M380B
Isotype IgG1
Target Name Serine / Threonine
Antigen Species Others
Immunogen Clone M380A was generated from a phosphothreonine synthetic peptide (coupled to carrier protein) and Clone M380B was generated from a phosphoserine synthetic peptide (coupled to carrier protein).
Conjugation Un-conjugated

Application Instructions

Application Suggestion
Tested Application Dilution
ELISA1:1000
ICC/IF1:50
IP1:50
WB1:500
Application Note WB: Antibody is suggested to be diluted in 5% skimmed milk/Tris buffer with 0.04% Tween20 and incubated for 1 hour at room temperature.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Purification Purification with Protein A.
Buffer PBS, 0.05% Sodium azide, 50% Glycerol and 1 mg/ml BSA.
Preservative 0.05% Sodium azide
Stabilizer 50% Glycerol and 1 mg/ml BSA
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Background Phosphorylation of specific serine or threonine residues is an important post-translational modification for regulating the activity of most proteins. Stimulation of a variety of cell signaling pathways activates the receptor and non-receptor ser/thr kinases that mediate these protein modifications. Antibodies that can detect phosphoserine or phosphothreonine residues are excellent tools for characterizing changes in the post-translational state of a broad range of phosphorylated proteins. Immunoprecipitation of proteins of interest followed by detection of phosphoserine or phosphothreonine using anti-phosphoserine antibody is commonly used to correlate changes in phosphorylation state with alterations in protein activity.

Images (2) Click the Picture to Zoom In

  • ARG23897 anti-Phosphoserine / threonine antibody [M380A + M380B] WB image

    Western blot: A431 cells treated with calyculin A (100 nM) for 30 min (lane 1 and 2) then treated with lambda phosphatase (lane 3). The blot was stained with ARG23897 anti-Phosphoserine / threonine antibody [M380A + M380B] at 1:250 (lane 1) or 1:1000 (lanes 2 and 3).

  • ARG23897 anti-Phosphoserine / threonine antibody [M380A + M380B] ICC/IF image

    Immunofluorescence: Control (left) and calyculin A-treated (right) A431 cells were stained with ARG23897 anti-Phosphoserine / threonine antibody [M380A + M380B].