Anti-STAT5a + STAT5b antibody [EPR16668]
- RabMAb
- Recombinant
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(3 Publications)
Rabbit Recombinant Monoclonal STAT5a antibody. Suitable for WB, ICC/IF, Flow Cyt (Intra), IHC-P and reacts with Rat, Mouse, Recombinant full length protein - Human, Recombinant full length protein - Mouse, Human samples. Cited in 3 publications.
View Alternative Names
STAT5, STAT5A, Signal transducer and activator of transcription 5A
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-STAT5a + STAT5b antibody [EPR16668] (AB200341)
Immunohistochemical analysis of paraffin-embedded Human tonsil tissue labeling STAT5b with ab200341 at 1/100 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution.
Cytoplasm and nuclear staining on Human tonsil tissue is observed.
Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-STAT5a + STAT5b antibody [EPR16668] (AB200341)
Intracellular flow cytometric analysis of 2% paraformaldehyde-fixed NIH/3T3 (Mouse embyro fibroblast cells) cells labeling STAT5b with ab200341 at 1/80 dilution (red) compared with a rabbit monoclonal IgG isotype control (ab172730;black) and an unlabelled control (cells without incubation with primary antibody and secondary antibody; blue). Goat anti rabbit IgG (FITC) at 1/150 dilution was used as the secondary antibody.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-STAT5a + STAT5b antibody [EPR16668] (AB200341)
Immunohistochemical analysis of paraffin-embedded Rat cardiac muscle tissue labeling STAT5b with ab200341 at 1/100 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution.
Cytoplasm and nuclear staining on rat cardiac muscle tissue is observed.
Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-STAT5a + STAT5b antibody [EPR16668] (AB200341)
Immunofluorescent analysis of 4% paraformaldehyde-fixed 0.1% Triton X-100 permeabilized C6 (Rat glial tumor cells) cells labeling STAT5b with ab200341 at 1/500 dilution followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green).
Nuclear and cytoplasm staining on C6 cell line is observed.
The nuclear counter stain is DAPI (blue).
Tubulin is detected with ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution and ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution (red).
The negative controls are as follows :
-ve control 1 : ab200341 at 1/500 dilution followed by ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution.
-ve control 2 : ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution followed by ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/500 dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-STAT5a + STAT5b antibody [EPR16668] (AB200341)
Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling STAT5b with ab200341 at 1/100 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution.
Cytoplasm and nuclear staining on mouse liver tissue is observed.
Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-STAT5a + STAT5b antibody [EPR16668] (AB200341)
Immunofluorescent analysis of 4% paraformaldehyde-fixed 0.1% Triton X-100 permeabilized RAW 264.7 (Mouse macrophage cells transformed with Abelson murine leukemia virus) cells labeling STAT5b with ab200341 at 1/500 dilution followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green).
Nuclear and cytoplasm staining on RAW 264.7 cell line is observed.
The nuclear counter stain is DAPI (blue). Tubulin is detected with ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution and ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution (red).
The negative controls are as follows :
-ve control 1 : ab200341 at 1/500 dilution followed by ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution.
-ve control 2 : ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution followed by ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/500 dilution.
- WB
Supplier Data
Western blot - Anti-STAT5a + STAT5b antibody [EPR16668] (AB200341)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-STAT5a + STAT5b antibody [EPR16668] (ab200341) at 1/1000 dilution
Lane 1:
K562 (Human chronic myelogenous leukemia cells from bone marrow) whole cell lysate at 10 µg
Lane 2:
Jurkat (Human T cell leukemia cells from peripheral blood) whole cell lysate at 10 µg
Lane 3:
Daudi (Human Burkitt's lymphoma cell line) whole cell lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 90 kDa
Observed band size: 90 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-STAT5a + STAT5b antibody [EPR16668] (AB200341)
Blocking/Dilution buffer : 5% NFDM/TBST.
ab200341 show cross reactivity with STAT5a. Full length human Stat5a recombinant protein contains aa1-794 with MYC/DDDDK tag.
All lanes:
Western blot - Anti-STAT5a + STAT5b antibody [EPR16668] (ab200341) at 1/200 dilution
All lanes:
Full length human Stat5a recombinant protein at 0.01 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 90 kDa
Observed band size: 90 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-STAT5a + STAT5b antibody [EPR16668] (AB200341)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-STAT5a + STAT5b antibody [EPR16668] (ab200341) at 1/1000 dilution
Lane 1:
C6 (Rat glial tumor cells) whole cell lysate at 10 µg
Lane 2:
PC-12 (Rat adrenal gland pheochromocytoma) whole cell lysate at 10 µg
Lane 3:
NIH/3T3 (Mouse embyro fibroblast cells) whole cell lysate at 10 µg
Lane 4:
Mouse heart lysate at 10 µg
Lane 5:
Rat heart lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 90 kDa
Observed band size: 90 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-STAT5a + STAT5b antibody [EPR16668] (AB200341)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-STAT5a + STAT5b antibody [EPR16668] (ab200341) at 1/10000 dilution
All lanes:
Recombinant protein fragment mouse Stat5b at 0.01 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 90 kDa
false
Exposure time: 3min
Related conjugates and formulations (1)
-
Anti-STAT5a+STAT5b antibody [EPR16668] - BSA and Azide free
Reactivity data
Product details
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
They are involved in mediating cytokine signaling by forming homo- or heterodimers upon phosphorylation by Janus kinases (JAKs). In the cytoplasm the formation of these dimers allows STAT5 to interact with DNA in the nucleus leading to the transcription of various genes important for cell proliferation differentiation and apoptosis. STAT5 has a significant role in cell cycle control and immune responses. The dimerization process involves complex formation and is an important part of its intracellular signaling cascade.
Pathways
STAT5a and STAT5b operate prominently within the JAK-STAT pathway. They are activated by proteins such as IL-2 IL-3 and Growth Hormone leading to transcriptional activity that affects growth and survival across various cell types. Besides the JAK-STAT pathway STAT5 interacts closely with the PI3K/AKT pathway thereby linking to cell survival signals. The cross-talk between these pathways enables fine-tuning of cellular responses to external stimuli and integrates signals from diverse receptors and ligands.
Product protocols
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Target data
Additional targets
Publications (3)
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American journal of respiratory cell and molecular biology 71:169-181 PubMed38593442
2024
Applications
Unspecified application
Species
Unspecified reactive species
Scientific reports 11:21608 PubMed34732817
2021
Applications
Unspecified application
Species
Unspecified reactive species
Biochemistry and biophysics reports 27:101052 PubMed34179518
2021
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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