Anti-Tyrosine Hydroxylase (phospho S40) antibody [EPR26191-5] - BSA and Azide free
- BOND RX™ Validated
- Recombinant
- RabMAb
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Rabbit Recombinant Monoclonal Tyrosine Hydroxylase phospho S40 antibody. Carrier free. Suitable for Dot, WB, IHC-P, IP and reacts with Synthetic peptide - Mouse, Mouse, Rat samples.
View Alternative Names
Tyrosine 3-monooxygenase, Tyrosine 3-hydroxylase, TH, Th
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Tyrosine Hydroxylase (phospho S40) antibody [EPR26191-5] - BSA and Azide free (AB316311)
This data was developed using ab316310, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse striatum tissue labeling Tyrosine Hydroxylase (phospho S40) with ab316310 at 1/2000 (0.252 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse striatum without alkaline phosphatase treatment (image A), no signal was detected when tissues were treated with alkaline phosphatase (image B). The section was incubated with ab316310 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Tyrosine Hydroxylase (phospho S40) antibody [EPR26191-5] - BSA and Azide free (AB316311)
This data was developed using ab316310, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse adrenal gland tissue labeling Tyrosine Hydroxylase (phospho S40) with ab316310 at 1/2000 (0.252 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse adrenal gland without alkaline phosphatase treatment (image A), no signal was detected when tissues were treated with alkaline phosphatase (image B). The section was incubated with ab316310 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Tyrosine Hydroxylase (phospho S40) antibody [EPR26191-5] - BSA and Azide free (AB316311)
This data was developed using ab316310, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat adrenal gland tissue labeling Tyrosine Hydroxylase (phospho S40) with ab316310 at 1/5000 (0.101 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat adrenal gland without alkaline phosphatase treatment (image A), no signal was detected when tissues were treated with alkaline phosphatase (image B). The section was incubated with ab316310 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IP
Supplier Data
Immunoprecipitation - Anti-Tyrosine Hydroxylase (phospho S40) antibody [EPR26191-5] - BSA and Azide free (AB316311)
This data was developed using ab316310, the same antibody clone in a different buffer formulation.
Tyrosine Hydroxylase (phospho S40) was immunoprecipitated from 0.35 mg Mouse striatum treated with 10μM forskolin for 10 minutes whole cell lysate with ab316310 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab316310 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Mouse striatum treated with 10μM forskolin for 10 minutes whole cell lysate
Lane 2 : ab316310 IP in Mouse striatum treated with 10μM forskolin for 10 minutes whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab316310 in Mouse striatum treated with 10μM forskolin for 10 minutes whole cell lysate
All lanes:
Immunoprecipitation - Anti-Tyrosine Hydroxylase (phospho S40) antibody [EPR26191-5] (<a href='/en-us/products/primary-antibodies/tyrosine-hydroxylase-phospho-s40-antibody-epr26191-5-ab316310'>ab316310</a>) at 1/30 dilution
All lanes:
Mouse striatum treated with 10µM forskolin for 10 minutes whole cell lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 48s
- IP
Supplier Data
Immunoprecipitation - Anti-Tyrosine Hydroxylase (phospho S40) antibody [EPR26191-5] - BSA and Azide free (AB316311)
This data was developed using ab316310, the same antibody clone in a different buffer formulation.
Tyrosine Hydroxylase (phospho S40) was immunoprecipitated from 0.35 mg PC-12 (rat adrenal gland pheochromocytoma cell) treated with 30μM forskolin for 60 minutes whole cell lysate with ab316310 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab316310 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : PC-12 (rat adrenal gland pheochromocytoma cell) treated with 30μM forskolin for 60 minutes whole cell lysate
Lane 2 : ab316310 IP in PC-12 (rat adrenal gland pheochromocytoma cell) treated with 30μM forskolin for 60 minutes whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab316310 in PC-12 treated with 30μM forskolin for 60 minutes whole cell lysate
All lanes:
Immunoprecipitation - Anti-Tyrosine Hydroxylase (phospho S40) antibody [EPR26191-5] (<a href='/en-us/products/primary-antibodies/tyrosine-hydroxylase-phospho-s40-antibody-epr26191-5-ab316310'>ab316310</a>) at 1/30 dilution
All lanes:
PC-12 (rat adrenal gland pheochromocytoma cell) treated with 30µM forskolin for 60 minutes whole cell lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 3s
- WB
Supplier Data
Western blot - Anti-Tyrosine Hydroxylase (phospho S40) antibody [EPR26191-5] - BSA and Azide free (AB316311)
This data was developed using ab316310, the same antibody clone in a different buffer formulation.
Tyrosine Hydroxylase (phospho S40) expression can be induced by forskolin treatment (PMID : 17157277).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
In Western blot, Anti-Tyrosine Hydroxylase antibody - Total protein control (ab137869) staining at 1/1000 dilution.
All lanes:
Western blot - Anti-Tyrosine Hydroxylase (phospho S40) antibody [EPR26191-5] (<a href='/en-us/products/primary-antibodies/tyrosine-hydroxylase-phospho-s40-antibody-epr26191-5-ab316310'>ab316310</a>) at 1/1000 dilution
Lane 1:
Untreated Mouse striatum tissue lysate (untreated membrane) at 20 µg
Lane 2:
Mouse striatum treated with 10uM forskolin for 10 minutes whole cell lysate (untreated membrane) at 20 µg
Lane 3:
Untreated Mouse striatum tissue lysate (alkaline phosphatase treated membrane) at 20 µg
Lane 4:
Mouse striatum treated with 10uM forskolin for 10 minutes whole cell lysate (alkaline phosphatase treated membrane) at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Observed band size: 58 kDa,36 kDa
false
Exposure time: 136s
- WB
Supplier Data
Western blot - Anti-Tyrosine Hydroxylase (phospho S40) antibody [EPR26191-5] - BSA and Azide free (AB316311)
This data was developed using ab316310, the same antibody clone in a different buffer formulation.
Tyrosine Hydroxylase (phospho S40) expression can be induced by forskolin treatment (PMID : 17157277).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
In Western blot, Anti-Tyrosine Hydroxylase antibody - Total protein control (ab137869) staining at 1/1000 dilution.
All lanes:
Western blot - Anti-Tyrosine Hydroxylase (phospho S40) antibody [EPR26191-5] (<a href='/en-us/products/primary-antibodies/tyrosine-hydroxylase-phospho-s40-antibody-epr26191-5-ab316310'>ab316310</a>) at 1/1000 dilution
Lane 1:
Untreated PC-12 (rat adrenal gland pheochromocytoma cell) whole cell lysate (untreated membrane) at 20 µg
Lane 2:
PC-12 treated with 30uM forskolin for 60 minutes whole cell lysate (untreated membrane) at 20 µg
Lane 3:
PC-12 treated with 30uM forskolin for 60 minutes whole cell lysate (alkaline phosphatase treated membrane) at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Observed band size: 58 kDa,36 kDa
false
Exposure time: 3s
- Dot
Supplier Data
Dot Blot - Anti-Tyrosine Hydroxylase (phospho S40) antibody [EPR26191-5] - BSA and Azide free (AB316311)
This data was developed using ab316310, the same antibody clone in a different buffer formulation.
Dot blot analysis of Tyrosine Hydroxylase (phospho S40) using ab316310 at 1 : 1000 (0.504 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Dot Blot - Anti-Tyrosine Hydroxylase (phospho S40) antibody [EPR26191-5] (<a href='/en-us/products/primary-antibodies/tyrosine-hydroxylase-phospho-s40-antibody-epr26191-5-ab316310'>ab316310</a>) at 1/1000 dilution
Lane 1:
Tyrosine Hydroxylase (phospho S40) peptide a
Lane 2:
Tyrosine Hydroxylase (phospho S40) peptide b
Lane 3:
Tyrosine Hydroxylase non-phospho peptide c
Secondary
All lanes:
Dot Blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
false
Exposure time: 180s
Related conjugates and formulations (1)
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Anti-Tyrosine Hydroxylase (phospho S40) antibody [EPR26191-5]
Reactivity data
Product details
ab316311 is the carrirer-free version of ab316310.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Tyrosine hydroxylase is essential for synthesizing catecholamines including dopamine norepinephrine and epinephrine. This enzyme associates with other components in the catecholamine biosynthetic pathway. It functions as part of a larger complex within certain cells where its action determines levels of important neurotransmitters. These neurotransmitters help regulate numerous central and peripheral nervous system activities.
Pathways
Tyrosine hydroxylase acts as a critical component in both the dopaminergic and adrenergic pathways. In the dopaminergic pathway tyrosine hydroxylase facilitates dopamine production influencing various physiological processes. The enzyme also correlates with ardrd protein in these pathways allowing fine-tuned control of neurotransmitter synthesis. Proteins related to tyrosine hydroxylase in these pathways include aromatic L-amino acid decarboxylase which further processes L-DOPA into dopamine.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com