Goat anti-rat IgG H&L (HRP) is a secondary antibody for chemiluminescent detection. Ideal for western blot. Suitable for ICC, IHC, western blot and ELISA.
- Cited in over 140 publications
Application | Reactivity | Dilution info | Notes |
---|---|---|---|
Application ICC | Reactivity Reacts | Dilution info - | Notes - |
Application IHC-P | Reactivity Reacts | Dilution info 1/200.00000 - 1/5000.00000 | Notes - |
Application ELISA | Reactivity Reacts | Dilution info 1/10000.00000 - 1/100000.00000 | Notes (as primary) |
Application WB | Reactivity Reacts | Dilution info 1/2000.00000 - 1/20000.00000 | Notes Colorimetric: Use 1/5000-1/30000, Chemiluminescent: use 1/10000-1/50000 |
Ig gamma-1 chain C region
Goat anti-rat IgG H&L (HRP) is a secondary antibody for chemiluminescent detection. Ideal for western blot. Suitable for ICC, IHC, western blot and ELISA.
- Cited in over 140 publications
By immunoelectrophoresis and ELISA this antibody reacts specifically with Rat IgG and with light chains common to other Rat immunoglobulins. No antibody was detected against non-immunoglobulin serum proteins.
pH: 6.8 - 7.4
Preservative: 0.05% CMIT/MIT based preservative
Constituents: 0.2% BSA
This antibody was isolated by affinity chromatography using antigen coupled to agarose beads and conjugated to Horse Radish Peroxidase (HRP).
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IHC image of alpha tubulin staining in human colon formalin fixed paraffin embedded tissue section*. The section was pre-treated using pressure cooker heat mediated antigen retrieval with sodium citrate buffer (pH6) for 30mins. The section was incubated with ab64332, 5μg/ml overnight at +4°C. An HRP-conjugated secondary (ab97057, 1/200 dilution) was used for 1hr at room temperature. The section was counterstained with haematoxylin and mounted with DPX.
The inset negative control image is taken from an identical assay without primary antibody.
*Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre
SDS Page 10-20% gradient gel.
All lanes: Western blot - Anti-IZUMO1 antibody [125] - BSA and Azide free (Anti-IZUMO1 antibody [125] - BSA and Azide free ab211626) at 1/1000 dilution
Lane 1: mouse testis lysate
Lane 2: mouse sperm lysate
All lanes: Western blot - Goat Anti-Rat IgG H&L (HRP) (ab97057) at 1/10000 dilution
Predicted band size: 39 kDa
All lanes: Western blot - Anti-IZUMO1 antibody [125] - BSA and Azide free (Anti-IZUMO1 antibody [125] - BSA and Azide free ab211626) at 1/100 dilution
Lane 1: human testis lysate
Lane 2: human sperm lysate
All lanes: Western blot - Goat Anti-Rat IgG H&L (HRP) (ab97057) at 1/10000 dilution
Predicted band size: 39 kDa
The main band is as expected at 80 kDa since the target is heavily glycosylated and phosphorylated.
All lanes: Western blot - Anti-CD34 antibody [MEC 14.7] (Anti-CD34 antibody [MEC 14.7] ab8158) at 1 µg/mL
All lanes: Mouse Lung Membrane Tissue Lysate (ab171830) at 50 µg
All lanes: Western blot - Goat Anti-Rat IgG H&L (HRP) (ab97057) at 1/20000 dilution
Performed under reducing conditions.
Predicted band size: 40 kDa
Observed band size: 80 kDa
Exposure time: 2min
Additional bands at : 85 kDa. We are unsure as to the identity of these extra bands.
All lanes: Western blot - Anti-Tubulin antibody [YL1/2] - Loading Control (Anti-Tubulin antibody [YL1/2] - Loading Control ab6160) at 1 µg/mL
All lanes: HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 20 µg
Lanes 1 - 2: Western blot - Goat Anti-Rat IgG H&L (HRP) (ab97057) at 1/2000 dilution
Lanes 3 - 4: Western blot - Goat Anti-Rat IgG H&L (HRP) (ab97057) at 1/10000 dilution
Lanes 5 - 6: Western blot - Goat Anti-Rat IgG H&L (HRP) (ab97057) at 1/20000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 36 kDa
Observed band size: 52 kDa
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