Description
FITC-conjugated Goat anti-Rabbit IgG (H+L) (CABS011)
The FITC-conjugated Goat anti-Rabbit IgG (H+L) (CABS011) is a high-quality antibody developed for reliable detection and analysis of target proteins. This antibody is produced using high quality goat anti-rabbit IgG (H+L) antibodies conjugated to fluorescein isothiocyanate (FITC), providing strong signal detection with minimal background noise.This secondary antibody is ideal for researchers working with rabbit primary antibodies in immunofluorescence and flow cytometry experiments. Its high specificity for rabbit IgG ensures reliable and accurate detection of target proteins in various biological samples.
This antibody is validated for use in IF/ICC, FC applications and has demonstrated reactivity against Rabbit samples.
| Product Name: | FITC-conjugated Goat anti-Rabbit IgG (H+L) |
| SKU: | CABS011 |
| Size: | 100μL, 200μL |
| Reactivity: | Rabbit |
| Conjugate: | FITC. Ex:491nm. Em:516nm. |
| Immunogen: | This information is considered to be commercially sensitive. | ||||
| Tested Applications: | IF/ICC FC | ||||
| Recommended Dilution: |
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Secondary antibodies are affinity-purified antibodies which will work with target-specific primary antibody in the detection, sorting or purification of its specified target. Secondary antibodies offer increased versatility enabling users to use many detection systems (e.g. HRP, AP, fluorescence). They can also provide greater sensitivity through signal amplification as multiple secondary antibodies . Most commonly, secondary antibodies are generated by immunizing the host animal (different from host species of primary antibody) with a pooled population of normal immunoglobulins from the host species of primary antibody and can be further purified and modified (i.e. antibody fragmentation, label conjugation, etc.) to ensure well-characterized specificity to corresponding normal immunoglobulins.
| Purification Method | Affinity purification |
| RRID | AB_2769476 |
| Buffer Information | Store at -20℃. Avoid freeze / thaw cycles. Buffer: PBS with 0.025% Sodium Azide,0.75% BSA,50% glycerol,pH7.3. |
 | Immunofluorescence analysis of Hep G2 cells using ACLY Rabbit pAb (CAB15251' target='_blank' >A15251) at a dilution of 1:100 (40x lens). Secondary antibody: FITC Goat Anti-Rabbit IgG (H+L) (CAB15251' target='_blank' >A15251)/594 Goat Anti-Rabbit IgG(H+L) (CABS039) at 1:100 dilution. Blue: DAPI for nuclear staining. |
 | Flow cytometry: 1X10^6 K-562 cells (negative control,left) and A-431 cells (right) were surface-stained with Purified Rabbit anti-Human E-Cadherin mAb(5 μl/Test,orange line) or secondary antibody only (blue line). Non-fluorescently stained K-562 and A-431 cells were used as blank control (red line). FITC Goat Anti-Rabbit IgG (H+L)(CABS011, 1:200) was used as a secondary antibody. |
