Rabbit Recombinant Monoclonal Dihydrofolate reductase (DHFR) antibody. Suitable for IP, WB, IHC-P and reacts with Human, Mouse, Rat samples.
Preservative: 0.02% Sodium azide
Constituents: 50% Glycerol (glycerin, glycerine), 48% PBS, 0.87% Sodium chloride
IP | WB | IHC-P | |
---|---|---|---|
Human | Tested | Tested | Tested |
Mouse | Expected | Tested | Expected |
Rat | Expected | Tested | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/2000 | Notes - |
Species Rat | Dilution info 1/2000 | Notes - |
Species Human | Dilution info 1/2000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/100 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Key enzyme in folate metabolism. Contributes to the de novo mitochondrial thymidylate biosynthesis pathway. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis. Binds its own mRNA and that of DHFR2.
Dihydrofolate reductase, DHFR
Rabbit Recombinant Monoclonal Dihydrofolate reductase (DHFR) antibody. Suitable for IP, WB, IHC-P and reacts with Human, Mouse, Rat samples.
Preservative: 0.02% Sodium azide
Constituents: 50% Glycerol (glycerin, glycerine), 48% PBS, 0.87% Sodium chloride
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
Immunoprecipitating DHFR in HeLa whole cell lysate.
Lane 1: Rabbit control IgG instead of ab288373 in HeLa whole cell lysate. For western blotting,a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000)
Lane 2: ab288373 (2 μg)+ HeLa whole cell lysate (500 μg)
Lane 3: HeLa whole cell lysate (10 μg)
All lanes: Immunoprecipitation - Anti-Dihydrofolate reductase (DHFR) antibody [9B2] (ab288373)
Predicted band size: 21 kDa
All lanes: Western blot - Anti-Dihydrofolate reductase (DHFR) antibody [9B2] (ab288373) at 1/2000 dilution
Lane 1: HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate
Lane 2: Jurkat (Human T cell leukemia cell line from peripheral blood) whole cell lysate
Lane 3: K-562 (Human chronic myelogenous leukemia lymphoblast cell line ) whole cell lysate
Lane 4: Raji (Human Burkitt's lymphoma cell line) whole cell lysate
Lane 5: HEK-293T (Human epithelial cell line from embryonic kidney transformed with large T antigen) whole cell lysate
Lane 6: Rat heart tissue
Lane 7: Mouse kidney tissue
Lane 8: Mouse liver tissue
All lanes: Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 21 kDa
Observed band size: 22 kDa
IHC image of ab288373 diluted at 1:100 and staining in paraffin-embedded human breast cancer performed on a Leica Bond™ system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30 min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.
IHC image of ab288373 diluted at 1:100 and staining in paraffin-embedded human liver cancer performed on a Leica Bond™ system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30 min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.
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