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Multi-rAb HRP-Goat Rabbit Recombinant Secondary Antibody (H+L)
Description
Images & Validation
−| Tested Applications | DOT, ELISA, WB |
|---|---|
| Dilution range | 1:10,000-1:100,000 for ELISA, 1:10,000-1:200,000 for western blotting with ECL substrates (1:10,000-1:40,000 is suggested for most system). |
| Reactivity | Rabbit |
Key Properties
−| Antibody Type | Recombinant Antibody |
|---|---|
| Host | Goat |
| Clonality | Recombinant |
| Purity | The antibody was purified from culture media supernatant by immunoaffinity chromatography using Protein G beads. |
| Conjugation | HRP |
Storage & Handling
−| Storage | Store at -20°C. Stable for one year after shipment. |
|---|---|
| Form/Appearance | Liquid |
| Buffer/Preservatives | PBS with 50% glycerol, 10 mg/mL rAlbumin, 0.1% Proclin-300, pH 7.4. |
| Concentration | 1.0 mg/mL |
| Disclaimer | For research use only |
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Various lysates were subjected to SDS-PAGE followed by western blot with rabbit anti-TOM70 polyclonal antibody at dilution of 1:10000. Multi-rAb HRP-Goat Anti-Rabbit Recombinant Secondary Antibody (H+L) (orb2302687) was used at 1:20000 for detection.

Various lysates were subjected to SDS-PAGE followed by western blot with rabbit anti-PSMB1 polyclonal antibody at dilution of 1:10000. Multi-rAb HRP-Goat Anti-Rabbit Recombinant Secondary Antibody (H+L) (orb2302687) was used at 1:20000 for detection.

Various lysates were subjected to SDS-PAGE followed by western blot with rabbit anti-Beta Catenin polyclonal antibody at dilution of 1:50000. Multi-rAb HRP-Goat Anti-Rabbit Recombinant Secondary Antibody (H+L) (orb2302687) was used at 1:20000 for detection.

Various lysates were subjected to SDS-PAGE followed by western blot with rabbit anti-TDP43 recombinant antibody at dilution of 1:20000. Multi-rAb HRP-Goat Anti-Rabbit Recombinant Secondary Antibody (H+L) (orb2302687) was used at 1:20000 for detection.

PC-3 and Calyculin A treated PC-3 cell lysates were subjected to SDS-PAGE followed by western blot with rabbit anti-Phospho-EIF4B (Ser406) Recombinant antibody at dilution of 1:20000. Multi-rAb HRP-Goat Anti-Rabbit Recombinant Secondary Antibody (H+L) (orb2302687), leading competitor’s non cross-adsorbed and cross-adsorbed secondary antibodies were all used at 0.05 μg/mL for detection.

HEK-293 and HepG2 cell lysates were subjected to SDS-PAGE followed by western blot with rabbit anti-ZO-1 polyclonal antibody at dilution of 1:50000. Multi-rAb HRP-Goat Anti-Rabbit Recombinant Secondary Antibody (H+L) (orb2302687), leading competitor’s non cross-adsorbed and cross-adsorbed secondary antibodies were all used at 0.05 μg/mL for detection.

Various lysates were subjected to SDS-PAGE followed by western blot with Beta tubulin rabbit recombinant antibody at dilution of 1:20000. Two batches of Multi-rAb HRP-Goat Anti-Rabbit Recombinant Secondary Antibody (H+L) (orb2302687) were used at 1:20000 for detection.

Rabbit total IgG, Mouse total IgG, Rat total IgG, Pig total IgG, Human total IgG, Bovine total IgG were coated at 100 ng/well. 0.125 μg/mL Multi-rAb HRP-Goat Anti-Rabbit Recombinant Secondary Antibody (H+L) (orb2302687) was used for detection. The result indicates that orb2302694 is highly specific for rabbit IgG and does not react with other species tested in the experiment.
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Multi-rAb HRP-Goat Rabbit Recombinant Secondary Antibody (H+L) (orb2302687)
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