Custom Premix Selecting "Custom Premix" option means that all of the beads you have chosen will be premixed in manufacturing before the kit is sent to you.
A set of four different monoclonal antibodies specific for serine phosphorylation sites. Recognition is dependent on phosphorylation and the surrounding amino acid motif. Recognizes serine phosphorylated proteins in Arabidopsis, bacteria, chicken, human, maize, mouse, rat, tobacco, Xenopus, yeast, and zebrafish. Phosphorylation patterns in cell extracts may differ when probed with different antibodies.
Catalogue Number
525282
Brand Family
Calbiochem®
Application Data
Detection of phosphoserine-containing antibodies by immunoblotting. Samples: Whole cell lysate from A431 cells treated with pervanadate (all lates). Primary antibodies: PhosphoDetect™ Anti-Phosphoserine Mouse mAb (16B4) (Cat. No. 525280) (1 µg/ml), PhosphoDetect™ Anti-Phosphoserine Mouse mAb (1C8) (Cat. No. 525281) (1 µg/ml), PhosphoDetect™ Anti-Phosphoserine Mouse mAb (4A3) (Cat. No. 525283) (1 µg/ml), and PhosphoDetect™ Anti-Phosphoserine Mouse mAb (4A9) (Cat. No. 525284) (1 µg/ml). Detection: chemiluminescence. Detection of phosphoserine-containing antibodies by immunoblotting. Samples: Extract from rabbit muscle*. Primary antibodies: PhosphoDetect™ Anti-Phosphoserine Mouse mAb (16B4) (Cat. No. 525280) (1 µg/ml), PhosphoDetect™ Anti-Phosphoserine Mouse mAb (1C8) (Cat. No. 525281) (1 µg/ml), PhosphoDetect™ Anti-Phosphoserine Mouse mAb (4A3) (Cat. No. 525283) (1 µg/ml), and PhosphoDetect™ Anti-Phosphoserine Mouse mAb (4A9) (Cat. No. 525284) (1 µg/ml). Detection: chemiluminescence. *Positive control supplied with the antibody.
References
Product Information
Form
Lyophilized
Formulation
25 µg each antibody lyophilized from 2X PBS, PEG, sucrose and 200 µl control phosphoproteins lyophilized 20 mM Na₂HPO₄, 0.1% SDS.
Kit contains
25 μg of each of the Phosphoserine Antibodies including clones 1C8, 4A3, 4A9, and 16B4, Rabbit Muscle Positive Control, and a data sheet.
Positive control
Phosphoproteins purified from rabbit muscle (included)
Immunoblotting (see characteristics table) Immunoprecipitation (see characteristics table) ELISA (see characteristics table)
Application Comments
DO NOT use milk or casein for membrane blocking or antibody dilutions; use BSA. For immunoblotting with the positive control, use 20 µl/lane (minigel) for colorimetric detection of 5 µl/lane for chemiluminescent detection. The phosphorylation patterns in a given cell lysate may differ when probed with individual antibodies due to sequence specificity. Antibodies should be titrated for optimal results in individual systems.
Biological Information
Immunogen
phosphoserine-containing peptides or phosphoserine conjugated to KLH
Host
Mouse
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code
Blue Ice Only
Toxicity
Standard Handling
Storage
-20°C
Do not freeze
Ok to freeze
Special Instructions
Reconstitute each antibody with 1 ml H₂O (15 min, room temperature). Following reconstitution, aliquot and freeze (-70°C). Stock solutions are stable for up to 1 year at -70°C. Thaw aliquots at 37°C prior to use. Reconstitute the positive control with 200 µl H₂O. After complete solubilization, add 200 µl SDS-PAGE sample buffer and incubate for 5 min at 90°C. Following incubation, aliquot and freeze (-20°C). Avoid freeze/thaw cycles of all solutions.
Packaging Information
Transport Information
Supplemental Information
Kit contains
25 μg of each of the Phosphoserine Antibodies including clones 1C8, 4A3, 4A9, and 16B4, Rabbit Muscle Positive Control, and a data sheet.
Specifications
Global Trade Item Number
产品目录编号
GTIN
525282-1KITCN
04055977270655
Documentation
PhosphoDetect™ Phosphoserine Detection Kit 分析证书
标题
批号
525282
数据表
Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.
Revision
20-April-2009 JSW
Application
Immunoblotting (see characteristics table) Immunoprecipitation (see characteristics table) ELISA (see characteristics table)
Application Data
Detection of phosphoserine-containing antibodies by immunoblotting. Samples: Whole cell lysate from A431 cells treated with pervanadate (all lates). Primary antibodies: PhosphoDetect™ Anti-Phosphoserine Mouse mAb (16B4) (Cat. No. 525280) (1 µg/ml), PhosphoDetect™ Anti-Phosphoserine Mouse mAb (1C8) (Cat. No. 525281) (1 µg/ml), PhosphoDetect™ Anti-Phosphoserine Mouse mAb (4A3) (Cat. No. 525283) (1 µg/ml), and PhosphoDetect™ Anti-Phosphoserine Mouse mAb (4A9) (Cat. No. 525284) (1 µg/ml). Detection: chemiluminescence. Detection of phosphoserine-containing antibodies by immunoblotting. Samples: Extract from rabbit muscle*. Primary antibodies: PhosphoDetect™ Anti-Phosphoserine Mouse mAb (16B4) (Cat. No. 525280) (1 µg/ml), PhosphoDetect™ Anti-Phosphoserine Mouse mAb (1C8) (Cat. No. 525281) (1 µg/ml), PhosphoDetect™ Anti-Phosphoserine Mouse mAb (4A3) (Cat. No. 525283) (1 µg/ml), and PhosphoDetect™ Anti-Phosphoserine Mouse mAb (4A9) (Cat. No. 525284) (1 µg/ml). Detection: chemiluminescence. *Positive control supplied with the antibody.
Description
A set of 4 mouse monoclonal antibodies purified from serum-free culture supernatant by thiophilic adsorption and size exclusion chromatography. All 4 antibodies recognize phosphoserine. Supplied with a positive control consisting of phosphoproteins purified from rabbit muscle lysate by Fe3+-IDA affinity chromatography.
Background
Protein phosphorylation is the principal indicator of the activation of signaling pathways. The binding of a growth factor to its specific receptor catalyzes a complex cascade of intracellular signaling events, characterized by altering the phosphorylation of tyrosine, serine, or threonine residues of target proteins. The phosphorylation state is tightly regulated by the actions of protein kinases, which transfer a phosphate group from donor substrates such as ATP or GTP to serine, threonine, or tyrosine residues, and protein phosphatases, which dephosphorylate phosphorylated proteins, thereby restoring the particular phosphorylation system to its basal stage. Most kinases are either serine/threonine-specific or tyrosine-specific, while some kinases can phosphorylate all 3 types of hydroxy-bearing amino acids. Radioactive kinase assays utilizing 32P-γ-ATP as the donor substrate have been frequently employed to assess kinase activity, since the method is sensitive, convenient, and easily quantified. Recently, however, the generation of phosphoprotein-specific antibodies has advanced the development of non-radioactive kinase activity detection methods to comparable sensitivity as radioactive methods. Antibodies specific for phosphorylated epitopes recognize the phosphorylated amino acid in the context of the surrounding amino acid sequence. Recognition, therefore, depends on 2 criteria: 1) phosphorylation and 2) the surrounding amino acid motif. If one of the two criteria is not fulfilled, the antibody will not detect the phosphorylation site. Since the surrounding amino acid sequence varies between phosphorylation sites, certain proteins, though phosphorylated, may not be detected by a given antibody.
Host
Mouse
Immunogen
phosphoserine-containing peptides or phosphoserine conjugated to KLH
Positive control
Phosphoproteins purified from rabbit muscle (included)
Form
Lyophilized
Formulation
25 µg each antibody lyophilized from 2X PBS, PEG, sucrose and 200 µl control phosphoproteins lyophilized 20 mM Na₂HPO₄, 0.1% SDS.
Preservative
≤ 0.1% sodium azide (antibodies only)
Comments
DO NOT use milk or casein for membrane blocking or antibody dilutions; use BSA. For immunoblotting with the positive control, use 20 µl/lane (minigel) for colorimetric detection of 5 µl/lane for chemiluminescent detection. The phosphorylation patterns in a given cell lysate may differ when probed with individual antibodies due to sequence specificity. Antibodies should be titrated for optimal results in individual systems.
Storage
-20°C
Do Not Freeze
Ok to freeze
Special Instructions
Reconstitute each antibody with 1 ml H₂O (15 min, room temperature). Following reconstitution, aliquot and freeze (-70°C). Stock solutions are stable for up to 1 year at -70°C. Thaw aliquots at 37°C prior to use. Reconstitute the positive control with 200 µl H₂O. After complete solubilization, add 200 µl SDS-PAGE sample buffer and incubate for 5 min at 90°C. Following incubation, aliquot and freeze (-20°C). Avoid freeze/thaw cycles of all solutions.
