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Work with LifeSpan to design a custom immunohistochemistry to address your specific biological question. Outsource the entire localization process without having to worry about finding and characterizing target specific antibodies, sourcing and validating difficult-to-find tissues, and having the ability to interpret the resulting immunostaining in relation to complex human pathologies.

Test your therapeutic antibodies in immunohistochemistry against a broad panel of normal frozen human tissue types in order to determine potential unintended binding. Our non-GLP TCR services are designed on the FDA recommendation outlined in their "Points to Consider in the Manufacture and Testing of Monoclonal Antibody Products for Human Use".

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TAOK2 / TAO2 Antibody (phospho‑Ser181) LS‑C24
Note: This antibody replaces LS-C89981, LS-C54381, LS-C49253
TAO2 antibody LS-C24 is an unconjugated rabbit polyclonal antibody to TAO2 (TAOK2) from human, mouse, rat and other species. Validated for IHC and WB.
Catalog
Size
Price
LS-C24-100
100 µl
$375

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Product Description

TAOK2 / TAO2 Antibody (phospho-Ser181) for IHC, WB/Western LS-C24

Specifications

Target
Rat TAOK2 / TAO2
Synonyms
TAOK2, Kinase from chicken homolog C, HKFC-C, PSK, PSK-1, PSK1-BETA, TAO1, TAO kinase 2, TAO2, PSK1, KIAA0881, MAP3K17
Host
Rabbit
Reactivity
Rat, Human, Mouse, Dog, Xenopus (tested or 100% immunogen sequence identity)
Clonality
Polyclonal
Conjugations
Unconjugated
Purification
Immunoaffinity purified
Modifications
Unmodified
Applications
  • IHC (1:25)
  • Western blot (1:1000)
Performing IHC? See our complete line of Immunohistochemistry Reagents including antigen retrieval solutions, blocking agents ABC Detection Kits and polymers, biotinylated secondary antibodies, substrates and more.
Immunogen
TAOK2 / TAO2 antibody was raised against phosphopeptide corresponding to amino acid residues surrounding the phosphoSer181 of TAO2.
Epitope
pSer181
Specificity
Specific for the ~120k TAO2 phosphorylated at Ser181 in Western blots. Immunolabeling is completely eliminated by treatment with X phosphatase
Presentation
10 mM HEPES, pH 7.5, 150 mM NaCl, 0.1 mg/mL BSA, 50% Glycerol
Storage
Short term: -20°C; Long term: -20°C.
Restrictions
For research use only.
About TAOK2 / TAO2
Serine/threonine-protein kinase involved in different processes such as membrane blebbing and apoptotic bodies formation DNA damage response and MAPK14/p38 MAPK stress-activated MAPK cascade. Phosphorylates itself, MBP, activated MAPK8, MAP2K3, MAP2K6 and tubulins. Activates the MAPK14/p38 MAPK signaling pathway through the specific activation and phosphorylation of the upstream MAP2K3 and MAP2K6 kinases. Q9UL54 NM_004783 NP_004774.1


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Images

Western blot

Western blot of rat cortex lysate showing specific immunolabeling of the ~120k TAO2 phosphorylated at Ser181 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: l-Ptase). The blot is identical to the control except that it was incubated in l-Ptase (1200 units for 30 min) before being exposed to the Anti-Ser181 TAO2. The immunolabeling is completely eliminated by treatment with l-Ptase.
Western blot of rat cortex lysate showing specific immunolabeling of the ~120k TAO2 phosphorylated at Ser181 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: l-Ptase). The blot is identical to the control except that it was incubated in l-Ptase (1200 units for 30 min) before being exposed to the Anti-Ser181 TAO2. The immunolabeling is completely eliminated by treatment with l-Ptase.

Western blot

Western blot of rat cortex lysate showing specific immunolabeling of the ~120k TAO2 phosphorylated at Ser181 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: l-Ptase). The blot is identical to the control except that it was incubated in l-Ptase (1200 units for 30 min) before being exposed to the Anti-Ser181 TAO2. The immunolabeling is completely eliminated by treatment with l-Ptase.
Western blot of rat cortex lysate showing specific immunolabeling of the ~120k TAO2 phosphorylated at Ser181 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: l-Ptase). The blot is identical to the control except that it was incubated in l-Ptase (1200 units for 30 min) before being exposed to the Anti-Ser181 TAO2. The immunolabeling is completely eliminated by treatment with l-Ptase.

Western blot

Western blot of rat cortex lysate showing specific immunolabeling of the ~120k TAO2 phosphorylated at Ser181 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: l-Ptase). The blot is identical to the control except that it was incubated in l-Ptase (1200 units for 30 min) before being exposed to the Anti-Ser181 TAO2. The immunolabeling is completely eliminated by treatment with l-Ptase.
Western blot of rat cortex lysate showing specific immunolabeling of the ~120k TAO2 phosphorylated at Ser181 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: l-Ptase). The blot is identical to the control except that it was incubated in l-Ptase (1200 units for 30 min) before being exposed to the Anti-Ser181 TAO2. The immunolabeling is completely eliminated by treatment with l-Ptase.

Western blot

Western blot of rat cortex lysate showing specific immunolabeling of the ~120k TAO2 phosphorylated at Ser181 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: l-Ptase). The blot is identical to the control except that it was incubated in l-Ptase (1200 units for 30 min) before being exposed to the Anti-Ser181 TAO2. The immunolabeling is completely eliminated by treatment with l-Ptase.
Western blot of rat cortex lysate showing specific immunolabeling of the ~120k TAO2 phosphorylated at Ser181 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: l-Ptase). The blot is identical to the control except that it was incubated in l-Ptase (1200 units for 30 min) before being exposed to the Anti-Ser181 TAO2. The immunolabeling is completely eliminated by treatment with l-Ptase.

Requested From: United States
Date Requested: 10/15/2018

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