bsm-52574R
[Primary Antibody]
Tyrosine Hydroxylase (8B6) Monoclonal Antibody
DATASHEET
Host: Rabbit
Target Protein: Tyrosine Hydroxylase
Clonality: Monoclonal
Isotype: IgG
Entrez Gene: 7054
Swiss Prot: P07101
Source: Human Tyrosine Hydroxylase between 500 amino acid to C-terminus
Purification: Purified by Protein A.
Storage Buffer: 0.01M TBS(pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Storage: Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.
Background:
Neuronal Marker Tyrosine hydroxylase is involved in the conversion of tyrosine to dopamine. As the rate-limiting enzyme in the synthesis of catecholamines, tyrosine hydroxylase has a key role in the physiology of adrenergic neurons. Tyrosine hydroxylase is regularly used as a marker for dopaminergic neurons, which is particularly relevant for research into Parkinson's disease.
Size: 100ul
Concentration: 1ug/ul
Cross Reactive Species:
Human
Mouse
Rat
For research use only. Not intended for diagnostic or therapeutic use.
PRODUCT SPECIFIC PUBLICATIONS
- Zeng Hong. et al. Unbiased multitissue transcriptomic analysis reveals complex neuroendocrine regulatory networks mediated by spinal cord injury-induced immunodeficiency. J NEUROINFLAMM. 2023 Dec;20(1):1-24Read more>>
- Natlia Perin Schmidt. et al. Effect of Probiotic Lacticaseibacillus rhamnosus LB1.5 on Anxiety-like Behavior, Neuroprotection and Neuroinflammation Markers of Male Mice Fed a High-Fat Diet. NUTRIENTS. 2024 Jan;16(6):879Read more>>
VALIDATION IMAGES
Flow cytometric analysis of N2A cells with Tyrosine Hydroxylase (8B6) Monoclonal Antibody (bsm-52574R) at 1:50 dilution (red) compared with an unlabeled control (cells without incubation with primary antibody; black).
PC-12 cell lysate probed with Tyrosine Hydroxylase (8B6) Monoclonal Antibody (bsm-52574R) at 1:1000 overnight at 4°C followed by a conjugated secondary antibody for 60 minutes at 37°C.
IF(ICC) staining with Tyrosine Hydroxylase (8B6) Monoclonal Antibody (bsm-52574R) at 1:100 in N2A cells (green). The nuclear counterstain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilized with 0.25% Triton X100/PBS.
IF(ICC) staining with Tyrosine Hydroxylase (8B6) Monoclonal Antibody (bsm-52574R) at 1:100 in NIH/3T3 cells (green). The nuclear counterstain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilized with 0.25% Triton X100/PBS.
IF(ICC) staining with Tyrosine Hydroxylase (8B6) Monoclonal Antibody (bsm-52574R) at 1:100 in SH-SY5Y cells (green). The nuclear counterstain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilized with 0.25% Triton X100/PBS.
Paraformaldehyde-fixed and paraffin-embedded Mouse brain tissue incubated with Tyrosine Hydroxylase (8B6) Monoclonal Antibody (bsm-52574R) at 1:100, overnight at 4°C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.
Lane 1: Mouse Adrenal gland tissue lysates; Lane 2: Mouse Cerebrum tissue lysates; Lane 3: Rat Adrenal gland tissue lysates; Lane 4: Rat Cerebrum tissue lysates probed with Tyrosine Hydroxylase Monoclonal Antibody, Unconjugated (bsm-52574R) at 1:1000 dilution and 4°C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37˚C.
Paraformaldehyde-fixed, paraffin embedded (rat adrenal gland); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Incubation with (Tyrosine Hydroxylase (8B6)) Monoclonal Antibody, Unconjugated (bsm-52574R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
Paraformaldehyde-fixed, paraffin embedded (mouse brain); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Incubation with (Tyrosine Hydroxylase (8B6)) Monoclonal Antibody, Unconjugated (bsm-52574R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
Paraformaldehyde-fixed, paraffin embedded (human kidney); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Incubation with (Tyrosine Hydroxylase (8B6)) Monoclonal Antibody, Unconjugated (bsm-52574R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
Paraformaldehyde-fixed, paraffin embedded (human kidney); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Incubation with (Tyrosine Hydroxylase (8B6)) Monoclonal Antibody, Unconjugated (bsm-52574R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.