重组Anti-STAT5a+STAT5b抗体[EPR16668] - BSA and Azide free
Anti-STAT5a+STAT5b antibody [EPR16668] - BSA and Azide free
- RabMAb
- Recombinant
- 了解详情
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(1 Publication)
Rabbit Recombinant Monoclonal STAT5b antibody. Carrier free. Suitable for ICC/IF, WB, Flow Cyt (Intra), IHC-P and reacts with Mouse, Rat, Human, Recombinant full length protein - Human samples. Cited in 1 publication.
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Signal transducer and activator of transcription 5B, STAT5B
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-STAT5a+STAT5b antibody [EPR16668] - BSA and Azide free (AB251306)
This data was developed using ab200341, the same antibody clone in a different buffer formulation.
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] - BSA and Azide free (AB251306)
This data was developed using ab200341, the same antibody clone in a different buffer formulation.
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] - BSA and Azide free (AB251306)
This data was developed using ab200341, the same antibody clone in a different buffer formulation.
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] - BSA and Azide free (AB251306)
This data was developed using ab200341, the same antibody clone in a different buffer formulation.
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] - BSA and Azide free (AB251306)
This data was developed using ab200341, the same antibody clone in a different buffer formulation.
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] - BSA and Azide free (AB251306)
This data was developed using ab200341, the same antibody clone in a different buffer formulation.
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] - BSA and Azide free (AB251306)
This data was developed using ab200341, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-STAT5a + STAT5b antibody [EPR16668] (<a href='/products/primary-antibodies/stat5a-stat5b-antibody-epr16668-ab200341'>ab200341</a>) 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] - BSA and Azide free (AB251306)
This data was developed using ab200341, the same antibody clone in a different buffer formulation.
Blocking and 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] (<a href='/products/primary-antibodies/stat5a-stat5b-antibody-epr16668-ab200341'>ab200341</a>) 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] - BSA and Azide free (AB251306)
This data was developed using ab200341, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-STAT5a + STAT5b antibody [EPR16668] (<a href='/products/primary-antibodies/stat5a-stat5b-antibody-epr16668-ab200341'>ab200341</a>) 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] - BSA and Azide free (AB251306)
This data was developed using ab200341, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-STAT5a + STAT5b antibody [EPR16668] (<a href='/products/primary-antibodies/stat5a-stat5b-antibody-epr16668-ab200341'>ab200341</a>) 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
不同偶联物与剂型 (1)
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Anti-STAT5a + STAT5b antibody [EPR16668]
反应性数据
产品详情
ab251306 is the carrier-free version of ab200341.
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.
性能和储存信息
形式
纯化工艺
存储溶液
运输条件
推荐的短期储存条件
推荐的长期储存条件
储存信息
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
These targets influence many cellular functions and contribute to cell proliferation differentiation and apoptosis. STAT5a and STAT5b often act as part of a larger transcriptional complex that binds to DNA and activates gene expression. In the immune system these proteins help modulate responses by regulating cytokine production. Their activity also extends to mammary gland development where they regulate milk production genes and they have roles in hematopoiesis affecting the development of blood cell types.
Pathways
The functions of STAT5a and STAT5b integrate mainly within the JAK-STAT signaling pathway which is pivotal for relaying cytokine signals from the cell membrane to the nucleus. This pathway links directly to proteins such as Janus kinases (JAKs) that phosphorylate STAT5 initiating its activation. Another key pathway is the PI3K-Akt signaling pathway where STAT5 can interact with components like mTOR to regulate cell growth and survival. These pathways are central to maintaining cellular homeostasis and immune function.
产品实验方案
- Visit the General protocols
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靶点信息
其他靶点
文献 (1)
Recent publications for all applications. Explore the full list and refine your search
Nutrients 16: PubMed38732558
2024
Applications
Unspecified application
Species
Unspecified reactive species
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