Luciferase (Photinus pyralis) Goat Polyclonal Antibody
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Product Data | |
Applications | ELISA, IHC, IP, WB |
Recommended Dilution | Suitable for Immunoblotting (Western or Dot blot), ELISA, Immunoprecipitation, Immunhistochemistry and most Immunological methods requiring high titer and specificity. Recommended Dilutions: This product has been assayed against 1.0 µg of Luciferase [Firefly] in a standard sandwich ELISA using Peroxidase conjugated Affinity Purified anti-Goat IgG [H&L] (Goat) and ABTS (2,2'-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid]) as a substrate for 30 minutes at room temperature. A working dilution of 1:20000 to 1:100000 of the reconstitution concentration is suggested for this product. For Western Blot, a recommended working dilution is 1:2000 - 1:10000. |
Host | Goat |
Clonality | Polyclonal |
Immunogen | Luciferase [Firefly]. |
Specificity | Assay by immunoelectrophoresis resulted in a single precipitin arc against purified and partially purified Luciferase [Firefly]. Cross reactivity against Luciferase from other sources has not been determined |
Formulation | PBS, pH 7.2 containing 0.01% sodium azides as a preservative. State: Serum State: Lyophilized purified Ig fraction. |
Reconstitution Method | Restore with 2.0 ml of deionized water (or equivalent). |
Concentration | 95.0 mg/ml (by Refractometry) |
Purification | Prepared from monospecific antiserum by a delipidation and defibrination. |
Background | Luciferase from the firefly has become one of the more widely used reporter proteins for the study of gene expression. Luciferase catalyzes a bioluminescent reaction which requires the substrate luciferin as well as Mg2+ and ATP. Mixing these reagents with the cell extract containing luciferase, results in a flash of light that decays rapidly. This light can be detected by a luminometer. The total light emission is proportional to the luciferase activity of the sample. |
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