Mouse Monoclonal MAK antibody. Suitable for WB, IHC-P and reacts with Recombinant fragment - Human, Human, Rat samples. Immunogen corresponding to Recombinant Fragment Protein within Human MAK aa 250 to C-terminus.
pH: 7.3
Preservative: 0.02% Sodium azide
Constituents: 50% Glycerol (glycerin, glycerine), 1% BSA
WB | IHC-P | |
---|---|---|
Human | Tested | Tested |
Rat | Expected | Expected |
Recombinant fragment - Human | Tested | Not recommended |
Species | Dilution info | Notes |
---|---|---|
Species Recombinant fragment - Human | Dilution info 1/500.00000 - 1/2000.00000 | Notes - |
Species Human | Dilution info 1/500.00000 - 1/2000.00000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info 1/500.00000 - 1/2000.00000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/150 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info 1/150 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Recombinant fragment - Human | Dilution info - | Notes - |
Essential for the regulation of ciliary length and required for the long-term survival of photoreceptors (By similarity). Phosphorylates FZR1 in a cell cycle-dependent manner. Plays a role in the transcriptional coactivation of AR. Could play an important function in spermatogenesis. May play a role in chromosomal stability in prostate cancer cells.
Serine/threonine-protein kinase MAK, Male germ cell-associated kinase, MAK
Mouse Monoclonal MAK antibody. Suitable for WB, IHC-P and reacts with Recombinant fragment - Human, Human, Rat samples. Immunogen corresponding to Recombinant Fragment Protein within Human MAK aa 250 to C-terminus.
pH: 7.3
Preservative: 0.02% Sodium azide
Constituents: 50% Glycerol (glycerin, glycerine), 1% BSA
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.
Paraffin embedded carcinoma of human prostate tissue stained for MAK using ab279383 at 1/150 dilution in immunohistochemical analysis. Heat-induced epitope retrieval by 1mM EDTA in 10mM Tris buffer pH8.5 at 120°C for 3minutes.
Paraffin embedded carcinoma of human thyroid tissue stained for MAK using ab279383 at 1/150 dilution in immunohistochemical analysis. Heat-induced epitope retrieval by 1mM EDTA in 10mM Tris buffer pH8.5 at 120°C for 3minutes.
Paraffin embedded human pancreas tissue stained for MAK using ab279383 at 1/150 dilution in immunohistochemical analysis. Heat-induced epitope retrieval by 1mM EDTA in 10mM Tris buffer pH8.5 at 120°C for 3minutes.
Paraffin embedded human liver tissue stained for MAK using ab279383 at 1/150 dilution in immunohistochemical analysis. Heat-induced epitope retrieval by 1mM EDTA in 10mM Tris buffer pH8.5 at 120°C for 3minutes.
All lanes: Western blot - Anti-MAK antibody [OTI1G2] (ab279383) at 1/500 dilution
Lane 1: HEK-293T cell extract at 35 µg
Lane 2: HeLa cell extract at 35 µg
Lane 3: HepG2 cell extract at 35 µg
Predicted band size: 71 kDa
All lanes: Western blot - Anti-MAK antibody [OTI1G2] (ab279383) at 1/2000 dilution
Lane 1: HEK-293T cells transfected with the pCMV6-ENTRY control at 5 µg
Lane 2: HEK-293T cells transfected with pCMV6-ENTRY MAK at 5 µg
Predicted band size: 71 kDa
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