Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790)
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(24 Publications)
Suitable for WB. Cited in 24 publications.
View Alternative Names
Ig gamma 1 chain C region, Ig gamma 3 chain C region, Ig gamma 4 chain C region, Ig gamma chain C region, Ig gamma-2 chain C region, Ig kappa-b4 chain C region, Ig kappa-b5 chain C region, Ig kappa-b9 chain C region, Ig lambda chain C region, Immunoglobin heavy constant gamma 1, Immunoglobulin G, K-BAS
- WB
Lab
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using Licor blocking buffer before being incubated with ab32537 overnight at 4°C. Antibody binding was detected using a goat anti-rabbit Alexa Fluor® 790) ab175781 at a 1 : 10,000 dilution for 1hr at room temperature and then imaged using the Licor Odyssey CLx.
All lanes:
Western blot - Anti-ERK1 antibody [Y72] (<a href='/en-us/products/primary-antibodies/erk1-antibody-y72-ab32537'>ab32537</a>) at 1/1000 dilution
Lane 1:
HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 20 µg
Lane 2:
HEK293 (Human embryonic kidney cell line) Whole Cell Lysate at 20 µg
Lane 3:
Recombinant Human ERK1 protein (<a href='/en-us/products/unavailable/recombinant-human-erk1-protein-ab43623-ab43623'>ab43623</a>) (<a href='/en-us/products/unavailable/recombinant-human-erk1-protein-ab43623-ab43623'>ab43623</a>) at 20 µg
Lane 4:
Western blot - Recombinant Human ERK2 protein (<a href='/en-us/products/proteins-peptides/recombinant-human-erk2-protein-ab43625'>ab43625</a>) at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (ab175781) at 1/10000 dilution
Predicted band size: 43 kDa
Observed band size: 44 kDa
false
- WB
Lab
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using Licor blocking buffer before being incubated with ab52971 overnight at 4°C. Antibody binding was detected using ab175781 at a 1 : 10,000 dilution for 1hr at room temperature and then imaged using the Licor Odyssey CLx.
Secondary antibody - anti-rabbit Alexa Fluor 790, ab175781.
All lanes:
Western blot - Anti-Integrin beta 1 antibody [EP1041Y] (<a href='/en-us/products/primary-antibodies/integrin-beta-1-antibody-ep1041y-ab52971'>ab52971</a>) at 20 µg
Lane 1:
HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 20 µg
Lane 2:
HT 1080 (Human fibrosarcoma) Whole Cell Lysate at 20 µg
Lane 3:
U2OS (Human osteosarcoma cell line) Whole Cell Lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (ab175781) at 1/10000 dilution
Predicted band size: 88 kDa
Observed band size: 120 kDa,140 kDa
false
- WB
Lab
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 5% Milk before being incubated with ab18251 overnight at 4°C. Antibody binding was detected using ab175781 at a 1 : 10,000 dilution for 1hr at room temperature and then imaged using the Licor Odyssey CLx.
All lanes:
Western blot - Anti-alpha Tubulin antibody - Loading Control (<a href='/en-us/products/primary-antibodies/alpha-tubulin-antibody-loading-control-ab18251'>ab18251</a>) at 1 µg/mL
All lanes:
HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate (ab27252) at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (ab175781) at 1/10000 dilution
Predicted band size: 36 kDa
Observed band size: 50 kDa
false
- WB
Lab
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using Licor blocking buffer before being incubated with ab52866 overnight at 4°C. Antibody binding was detected using Anti-Rabbit Alexa Fluor® 790 (ab175781) at a 1 : 10,000 dilution for 1hr at room temperature and then imaged using the Licor Odyssey CLx.
All lanes:
Western blot - Anti-alpha Tubulin antibody [EP1332Y] - Loading Control (<a href='/en-us/products/primary-antibodies/alpha-tubulin-antibody-ep1332y-loading-control-ab52866'>ab52866</a>) at 1/1000 dilution
Lane 1:
HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 20 µg
Lane 2:
HEK293 (Human embryonic kidney cell line) Whole Cell Lysate at 20 µg
Lane 3:
HepG2 (Human hepatocellular liver carcinoma cell line) Whole Cell Lysate at 20 µg
Lane 4:
Caco 2 (Human colonic carcinoma cell line) Whole Cell Lysate at 20 µg
Lane 5:
NIH/3T3 (Mouse embryonic fibroblast cell line) Whole Cell Lysate at 20 µg
Lane 6:
PC-12 (Rat adrenal pheochromocytoma cell line) Whole Cell Lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (ab175781) at 1/10000 dilution
Predicted band size: 50 kDa
Observed band size: 52 kDa
false
- WB
Lab
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 5% Milk before being incubated with ab8227 overnight at 4°C. Antibody binding was detected using Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (ab175781) secondary antibody at a 1 : 10,000 dilution for 1hr at room temperature and then imaged using the Licor Odyssey CLx.
All lanes:
Western blot - Anti-beta Actin antibody - Loading Control (<a href='/en-us/products/primary-antibodies/beta-actin-antibody-loading-control-ab8227'>ab8227</a>) at 1/1000 dilution
Lane 1:
A431 (human epidermoid carcinoma cell line) Whole Cell Lysate at 20 µg
Lane 2:
HEK-293 (human epithelial cell line from embryonic kidney) Whole Cell Lysate at 20 µg
Lane 3:
NIH/3T3 (mouse embryo fibroblast cell line) Whole Cell Lysate at 20 µg
Lane 4:
PC-12 (rat adrenal gland pheochromocytoma cell line) Whole Cell Lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (ab175781) at 1/10000 dilution
Predicted band size: 41 kDa
Observed band size: 42 kDa
false
- WB
Lab
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using Licor blocking buffer before being incubated with ab18251 overnight at 4°C. Antibody binding was detected using Anti-Rabbit Alexa Fluor® 790 (ab175781) at a 1 : 10,000 dilution for 1hr at room temperature and then imaged using the Licor Odyssey CLx.
All lanes:
Western blot - Anti-alpha Tubulin antibody - Loading Control (<a href='/en-us/products/primary-antibodies/alpha-tubulin-antibody-loading-control-ab18251'>ab18251</a>) at 0.5 µg/mL
Lane 1:
HeLa (Human epithelial carcinoma cell line) whole cell lysate at 20 µg
Lane 2:
HEK-293 (Human embryonic kidney cell line) whole cell lysate at 20 µg
Lane 3:
HepG2 (Human hepatocellular liver carcinoma cell line) whole cell lysate at 20 µg
Lane 4:
Caco-2 (Human colonic carcinoma cell line) whole cell lysate at 20 µg
Lane 5:
NIH/3T3 (Mouse embryonic fibroblast cell line) whole cell lysate at 20 µg
Lane 6:
PC-12 (Rat adrenal pheochromocytoma cell line) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (ab175781) at 1/10000 dilution
Predicted band size: 27 kDa,50 kDa
Observed band size: 44 kDa,52 kDa
false
- WB
Lab
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using Licor blocking buffer before being incubated with ab52623 overnight at 4°C.
Antibody binding was detected using ab175781 at a 1 : 10,000 dilution for 1hr at room temperature and then imaged using the Licor Odyssey CLx.
All lanes:
Western blot - Anti-beta III Tubulin antibody [EP1569Y] - Neuronal Marker (<a href='/en-us/products/primary-antibodies/beta-iii-tubulin-antibody-ep1569y-neuronal-marker-ab52623'>ab52623</a>) at 1/1000 dilution
Lane 1:
Brain (Mouse) Tissue Lysate at 20 µg
Lane 2:
Brain (Rat) Tissue Lysate at 20 µg
Lane 3:
Spinal Cord (Mouse) Tissue Lysate at 20 µg
Lane 4:
Spinal Cord (Rat) Tissue Lysate at 20 µg
Lane 5:
PC-12 (Rat adrenal pheochromocytoma cell line) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (ab175781) at 1/10000 dilution
Predicted band size: 50 kDa
Observed band size: 52 kDa
false
- ELISA
Lab
ELISA - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
Cross-reactivity of the polyclonal secondary antibody ab182016 was tested using a sandwich ELISA approach. The wells were coated with the indicated IgG standards at 1 μg/ml (50 μl/well) and incubated overnight at 4°C, followed by a 5% BSA blocking step for 2h at RT. ab182016 was then added starting at 1 μg/ml and gradually diluted 1/4 (50 μl/well), followed by incubation for 2h. For the detection Donkey anti-Goat IgG H&L (HRP) (ab6885) was used at 1/10,000 dilution (50 μl/well), followed by incubation for 1h at RT.
For the batch tested, ab182016 showed a cross-reactivity of 5-7% towards Human IgG and below 2% towards Mouse IgG, Rat IgG and Chicken IgY.
This data was developed using the unconjugated antibody (ab182016).
- ELISA
Lab
ELISA - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
Cross-reactivity of Goat anti-Rabbit IgG H&L (ab182016) and Goat anti-Rabbit IgG H&L obtained from two different vendors was tested using a sandwich ELISA approach. The wells were coated with the indicated IgG standards (Rabbit, Human, Mouse and Rat) at 1 μg/ml (50 μl/well) and incubated overnight at 4°C, followed by a 5% BSA blocking step for 2h at RT. Secondary antibodies were then added starting at 1 μg/ml and gradually diluted 1/4 (50 μl/well), followed by incubation for 2h. For the detection Donkey anti-Goat IgG H&L (HRP) (ab6885) was used at 1/10,000 dilution (50 μl/well), followed by incubation for 1h at RT. This data is from a representative dilution.
This data was developed using the unconjugated antibody (ab182016).
- WB
Lab
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using Licor blocking buffer before being incubated with ab32081 overnight at 4°C. Antibody binding was detected using ab175781 (goat anti-rabbit Alexa Fluor 790) at a 1 : 10,000 dilution for 1hr at room temperature and then imaged using the Licor Odyssey CLx.
All lanes:
Western blot - Anti-ERK2 antibody [E460] (<a href='/en-us/products/primary-antibodies/erk2-antibody-e460-ab32081'>ab32081</a>) at 1/1000 dilution
Lane 1:
HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 20 µg
Lane 2:
HEK293 (Human embryonic kidney cell line) Whole Cell Lysate at 20 µg
Lane 3:
46C (Mouse neural progenitor, selected for Sox1 expression cell line) Whole Cell Lysate at 20 µg
Lane 4:
PC12 (Rat adrenal pheochromocytoma cell line) Whole Cell Lysate at 20 µg
Lane 5:
Recombinant Human ERK1 protein (<a href='/en-us/products/unavailable/recombinant-human-erk1-protein-ab43623-ab43623'>ab43623</a>) (<a href='/en-us/products/unavailable/recombinant-human-erk1-protein-ab43623-ab43623'>ab43623</a>) at 20 µg
Lane 6:
Western blot - Recombinant Human ERK2 protein (<a href='/en-us/products/proteins-peptides/recombinant-human-erk2-protein-ab43625'>ab43625</a>) at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (ab175781) at 1/10000 dilution
Predicted band size: 41 kDa
Observed band size: 41 kDa
false
- WB
Lab
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using Licor blocking buffer before being incubated with ab156302 overnight at 4°C. Antibody binding was detected using ab175781 at a 1/10,000 dilution for 1hr at room temperature and then imaged using the Licor Odyssey CLx.
Secondary antibody - goat anti-rabbit Alexa Fluor® 790 (ab175781).
All lanes:
Western blot - Anti-muscle Actin antibody [EPR8484] - Loading Control (<a href='/en-us/products/primary-antibodies/muscle-actin-antibody-epr8484-loading-control-ab156302'>ab156302</a>) at 1/1000 dilution
Lane 1:
A431 (Human epithelial carcinoma cell line) Whole Cell Lysate at 20 µg
Lane 2:
HEK293 (Human embryonic kidney cell line) Whole Cell Lysate at 20 µg
Lane 3:
MCF7 (Human breast adenocarcinoma cell line) Whole Cell Lysate at 20 µg
Lane 4:
HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 20 µg
Lane 5:
Skeletal Muscle (Human) Tissue Lysate - adult normal tissue at 20 µg
Lane 6:
NIH 3T3 (Mouse embryonic fibroblast cell line) Whole Cell Lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (ab175781) at 1/10000 dilution
Predicted band size: 42 kDa
Observed band size: 42 kDa
false
- WB
Lab
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using Licor blocking buffer before being incubated with ab52901 overnight at 4°C. Antibody binding was detected using ab175781 at a 1 : 10,000 dilution for 1hr at room temperature and then imaged using the Licor Odyssey CLx.
All lanes:
Western blot - Anti-beta Tubulin antibody [EP1331Y] - Loading Control (<a href='/en-us/products/primary-antibodies/beta-tubulin-antibody-ep1331y-loading-control-ab52901'>ab52901</a>) at 1/20000 dilution
Lane 1:
Brain (Mouse) Tissue Lysate at 20 µg
Lane 2:
Brain (Rat) Tissue Lysate at 20 µg
Lane 3:
Spinal Cord (Mouse) Tissue Lysate at 20 µg
Lane 4:
Spinal Cord (Rat) Tissue Lysate at 20 µg
Lane 5:
PC12 (Rat adrenal pheochromocytoma cell line) Whole Cell Lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (ab175781) at 1/10000 dilution
Predicted band size: 49 kDa
Observed band size: 52 kDa
false
- WB
Lab
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
This blot was produced using a 4-12% Bis-tris gel under the MES buffer system. The gel was run at 200V for 35 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using Licor blocking buffer before being incubated with ab175007 overnight at 4°C. Antibody binding was detected using ab175781 (goat anti-rabbit Alexa Fluor 790) at a 1 : 10,000 dilution for 1hr at room temperature and then imaged using the Licor Odyssey CLx.
All lanes:
Western blot - Anti-Histone H3 (asymmetric di methyl R2) antibody - ChIP Grade (<a href='/en-us/products/primary-antibodies/histone-h3-asymmetric-di-methyl-r2-antibody-chip-grade-ab175007'>ab175007</a>) at 1 µg/mL
Lane 1:
HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 10 µg
Lane 2:
HeLa Nuclear Prep (0.5% Triton X-100 insoluble fraction) at 10 µg
Lane 3:
NIH 3T3 (Mouse embryonic fibroblast cell line) Whole Cell Lysate at 10 µg
Lane 4:
Calf Thymus Histone Preparation Nuclear Lysate at 0.5 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (ab175781) at 1/10000 dilution
Predicted band size: 14 kDa,15 kDa,36 kDa,41 kDa,49 kDa
Observed band size: 17 kDa,18 kDa,37 kDa,42 kDa
false
- WB
Lab
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
This blot was produced using a 4-12% Bis-tris gel under the MES buffer system. The gel was run at 200V for 35 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using Licor blocking buffer before being incubated with ab177138 overnight at 4°C. Antibody binding was detected using ab175781 at a 1 : 10,000 dilution for 1hr at room temperature and then imaged using the Licor Odyssey CLx.
All lanes:
Western blot - Anti-Histone H2B (formyl K5) antibody (<a href='/en-us/products/primary-antibodies/histone-h2b-formyl-k5-antibody-ab177138'>ab177138</a>) at 1 µg/mL
Lane 1:
HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 10 µg
Lane 2:
HeLa Nuclear Prep (0.5% Triton X-100 insoluble fraction) at 10 µg
Lane 3:
NIH 3T3 (Mouse) Whole Cell Lysate at 10 µg
Lane 4:
Calf Thymus Histone Preparation Nuclear Lysate at 0.5 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (ab175781) at 1/10000 dilution
Predicted band size: 14 kDa
Observed band size: 18 kDa
false
- WB
Lab
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
This blot was produced using a 4-12% Bis-tris gel under the MES buffer system. The gel was run at 200V for 35 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using Licor blocking buffer before being incubated with ab177168 overnight at 4°C. Antibody binding was detected using ab175781 at a 1 : 10,000 dilution for 1hr at room temperature and then imaged using the Licor Odyssey CLx.
All lanes:
Western blot - Anti-Histone H2B (formyl K108) antibody (<a href='/en-us/products/primary-antibodies/histone-h2b-formyl-k108-antibody-ab177168'>ab177168</a>) at 1 µg/mL
Lane 1:
HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 10 µg
Lane 2:
HeLa Nuclear Prep (0.5% Triton X-100 insoluble fraction) at 10 µg
Lane 3:
NIH 3T3 (Mouse embryonic fibroblast cell line) Whole Cell Lysate at 10 µg
Lane 4:
Calf Thymus Histone Preparation Nuclear Lysate at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (ab175781) at 1/10000 dilution
Predicted band size: 14 kDa
Observed band size: 18 kDa,37 kDa
false
- WB
Unknown
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using Licor blocking buffer before being incubated with ab13585 overnight at 4°C. Antibody binding was detected using ab175781 at a 1 : 10,000 dilution for 1hr at room temperature and then imaged using the Licor Odyssey CLx.
All lanes:
Anti-MDC1 antibody (<a href='/en-us/products/unavailable/mdc1-antibody-ab13858'>ab13858</a>) at 1 µg/mL
Lane 1:
Hela whole cell lysate (Staurosporine treated, 2uM/4hr) at 20 µg
Lane 2:
Hela whole cell lysate (untreated control) at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (ab175781) at 1/10000 dilution
Predicted band size: 22 kDa,28 kDa,29 kDa,31 kDa,50 kDa
Observed band size: 17 kDa,19 kDa,32 kDa,36 kDa,43 kDa
false
- WB
Unknown
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (AB175781)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab52971).
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using Licor blocking buffer before being incubated with ab52971 overnight at 4°C. Antibody binding was detected using ab175781 at a 1 : 10,000 dilution for 1hr at room temperature and then imaged using the Licor Odyssey CLx.
Secondary antibody -anti-rabbit Alexa Fluor 790, ab175781
All lanes:
Western blot - Anti-Integrin beta 1 antibody [EP1041Y] - BSA and Azide free (<a href='/en-us/products/primary-antibodies/integrin-beta-1-antibody-ep1041y-bsa-and-azide-free-ab192456'>ab192456</a>) at 20 µg
Lane 1:
HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 20 µg
Lane 2:
HT 1080 (Human fibrosarcoma) Whole Cell Lysate at 20 µg
Lane 3:
U2OS (Human osteosarcoma cell line) Whole Cell Lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790) (ab175781) at 1/10000 dilution
Predicted band size: 88 kDa
Observed band size: 120 kDa,140 kDa
false
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667 Cy5®
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505 Cy2®
Goat Anti-Rabbit IgG H&L (Cy2 ®) preadsorbed
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519 FITC
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572 TRITC
Goat Anti-Rabbit IgG H&L (TRITC)
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Goat Anti-Rabbit IgG H&L (6nm Gold)
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618 DyLight® 594
Goat Anti-Rabbit IgG H&L (DyLight® 594)
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576 DyLight® 550
Goat Anti-Rabbit IgG H&L (DyLight® 550)
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673 DyLight® 650
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702 Alexa Fluor® 680
Goat Anti-Rabbit IgG H&L (Alexa Fluor® 680)
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603 Alexa Fluor® 568
Goat Anti-Rabbit IgG H&L (Alexa Fluor® 568)
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519 Alexa Fluor® 488
Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488)
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565 Alexa Fluor® 555
Goat Anti-Rabbit IgG H&L (Alexa Fluor® 555)
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665 Alexa Fluor® 647
Goat Anti-Rabbit IgG H&L (Alexa Fluor® 647)
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617 Alexa Fluor® 594
Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594)
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702 Alexa Fluor® 680
Goat Anti-Rabbit IgG H&L (Alexa Fluor® 680) preadsorbed
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Goat Anti-Rabbit IgG H&L (Biotin)
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Goat Anti-Rabbit IgG H&L (HRP)
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775 Alexa Fluor® 750
Goat Anti-Rabbit IgG H&L (Alexa Fluor® 750) preadsorbed
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421 Alexa Fluor® 405
Goat Anti-Rabbit IgG H&L (Alexa Fluor® 405)
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578 PE
Goat Anti-Rabbit IgG H&L (PE) preadsorbed
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615 Texas Red®
Goat Anti-Rabbit IgG H&L (Texas Red ®)
-
660 APC
Goat Anti-Rabbit IgG H&L (APC) preadsorbed
-
518 DyLight® 488
Goat Anti-Rabbit IgG H&L (DyLight® 488) preadsorbed
-
703 Cy5.5®
Goat Anti-Rabbit IgG H&L (Cy5.5 ®) preadsorbed
-
565 Cy3®
Goat Anti-Rabbit IgG H&L (Cy3 ®) preadsorbed
-
596 Cy3.5®
Goat Anti-Rabbit IgG H&L (Cy3.5 ®) preadsorbed
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Why is this recommended?
We recommend this product because it’s often used in the same experiment or related research.
We advise that you always check the datasheet to ensure it fits your experiments, or contact ourtechnical teamfor help.
Product details
We batch test Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790), ab175781 in fluorescent WB. Although we don't batch test for ICC, ELISA, IHC-Fr or Flow cytometry customers have had success using Goat Anti-Rabbit IgG H&L (Alexa Fluor® 790), ab175781 in these applications.
Alexa Fluor® is a registered trademark of Molecular Probes, Inc, a Thermo Fisher Scientific Company. The Alexa Fluor® dye included in this product is provided under an intellectual property license from Life Technologies Corporation. As this product contains the Alexa Fluor® dye, the purchase of this product conveys to the buyer the non-transferable right to use the purchased product and components of the product only in research conducted by the buyer (whether the buyer is an academic or for-profit entity). As this product contains the Alexa Fluor® dye the sale of this product is expressly conditioned on the buyer not using the product or its components, or any materials made using the product or its components, in any activity to generate revenue, which may include, but is not limited to use of the product or its components: in manufacturing; (ii) to provide a service, information, or data in return for payment (iii) for therapeutic, diagnostic or prophylactic purposes; or (iv) for resale, regardless of whether they are sold for use in research. For information on purchasing a license to this product for purposes other than research, contact Life Technologies Corporation, 5781 Van Allen Way, Carlsbad, CA 92008 USA or outlicensing@thermofisher.com.
Properties and storage information
Form
Purification technique
Purification notes
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
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Publications (24)
Recent publications for all applications. Explore the full list and refine your search
Animal nutrition (Zhongguo xu mu shou yi xue hui) 16:34-44 PubMed38131029
2023
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Science advances 9:eadi4148 PubMed37624885
2023
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Neuroreport 34:348-356 PubMed36966805
2023
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Food science & nutrition 11:493-503 PubMed36655066
2023
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Microbiology spectrum 10:e0294922 PubMed36377917
2022
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Journal of neuroinflammation 19:253 PubMed36217178
2022
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Frontiers in cellular and infection microbiology 12:967149 PubMed36176578
2022
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Cell death discovery 8:228 PubMed35468892
2022
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Open medicine (Warsaw, Poland) 17:566-576 PubMed35415247
2022
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Bioengineered 13:6942-6954 PubMed35249453
2022
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