biological source
goat
conjugate
biotin conjugate
antibody form
affinity purified immunoglobulin
antibody product type
secondary antibodies
clone
polyclonal
species reactivity
mouse
manufacturer/tradename
Chemicon®
technique(s)
ELISA: suitable, flow cytometry: suitable, immunocytochemistry: suitable, immunohistochemistry: suitable (paraffin), western blot: suitable
isotype
IgG
shipped in
wet ice
target post-translational modification
unmodified
Quality Level
General description
25 kDa
Antibody molecules typically comprise two immunoglobulin light chains covalently bound to a pair of heavy chains. Immunoglobulin light chains occur in two types, designated by the Greek letters kappa and lambda. Kappa and gamma light chains are approximately 250 amino acids in length with an average mass of about 25 kDa. The ratio of kappa to lambda found in the immunoglobulin population varies by species.
Immunogen
Epitope: Kappa light chain
Prepared from purified mouse IgG light chain.
Application
Suggested dilutions:
Western Blotting: 1:20,000 - 1:400,000 of the 1 mg/mL stock
ELISA: 1:20,000 - 1:400,000 of the 1 mg/mL stock
Immunohistochemistry: 1:500 - 1:5,000 of the 1 mg/mL stock
Immunocytochemistry: 1:500 - 1:5,000 of the 1 mg/mL stock
Flow Cytometry: 1:200 - 1:1,000 of the 1 mg/mL stock
Optimal working dilutions must be determined by the end user.
Western Blotting: 1:20,000 - 1:400,000 of the 1 mg/mL stock
ELISA: 1:20,000 - 1:400,000 of the 1 mg/mL stock
Immunohistochemistry: 1:500 - 1:5,000 of the 1 mg/mL stock
Immunocytochemistry: 1:500 - 1:5,000 of the 1 mg/mL stock
Flow Cytometry: 1:200 - 1:1,000 of the 1 mg/mL stock
Optimal working dilutions must be determined by the end user.
Detect Mouse light chain using this Goat anti-Mouse light chain Antibody, biotin conjugate validated for use in ELISA, FC, WB, IC, IH(P).
Research Category
Secondary & Control Antibodies
Secondary & Control Antibodies
Research Sub Category
Fragment Specific Secondary Antibodies
Fragment Specific Secondary Antibodies
Biochem/physiol Actions
Minimal cross-reaction with bovine, goat, horse, human, rabbit, rat, and sheep.
The antibody reacts strongly with native primary antibodies primarily with kappa light chains. It is not suitable for detecting lambda light chains. The antibody does not react with the heavy chain of mouse IgG. The antibody has been tested by ELISA and adsorbed to ensure minimal cross-reaction with bovine, goat, horse, human, rabbit, rat, and sheep immunoglobulins.
Physical form
ImmunoAffinity Purified
Lyophilized powder from a solution with 0.01M Sodium Phosphate, 0.25M NaCl, pH 7.6, 0.05% Sodium Azide. 15 mg/mL BSA as stabilizer. Purified by immunoaffinity chromatography.
Preparation Note
Maintain lyophilized product at 2°-8°C for up to 12 months. After reconstitution the product is stable for six weeks at 2°-8°C in the dark as an undiluted liquid. Reconstitute vial with of distilled water (addition of 0.5 ml water will yield a final concentration of 1 mg/mL). For extended storage after reconstitution, add an equal volume of glycerol to make a final concentration of 50% glycerol followed by storage at -20°C in undiluted aliquots for up to 12 months. Please note the concentration of protein (and buffer salts) will decrease to one-half of the original after the addition of glycerol. Avoid repeated freeze thaw cycles. Keep away from light.
Legal Information
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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hcodes
pcodes
Hazard Classifications
Aquatic Chronic 3
存储类别
11 - Combustible Solids
wgk
WGK 3
Practical implementation, characterization and applications of a multi-colour time-gated luminescence microscope.
Zhang, L; Zheng, X; Deng, W; Lu, Y; Lechevallier, S; Ye, Z; Goldys, EM; Dawes, JM; Piper et al.
Scientific Reports null
Dayong Jin et al.
Journal of biomedical optics, 14(2), 024023-024023 (2009-05-02)
A fundamental problem for rare-event cell analysis is auto-fluorescence from nontarget particles and cells. Time-gated flow cytometry is based on the temporal-domain discrimination of long-lifetime (>1 micros) luminescence-stained cells and can render invisible all nontarget cell and particles. We aim
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