Anti-Pit1 antibody [EPR28191-52] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal PIT1 antibody. Carrier free. Suitable for IHC-P, WB and reacts with Human, Mouse, Rat, Transfected cell lysate - Human samples.
View Alternative Names
GHF1, PIT1, POU1F1, Pituitary-specific positive transcription factor 1, PIT-1, Growth hormone factor 1, GHF-1
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pit1 antibody [EPR28191-52] - BSA and Azide free (AB313643)
This data was developed using ab313642, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded human liver tissue labeling Pit1 with ab313642 at 1/100 (5.25 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : no staining on human liver.The section was incubated with ab313642 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrumentIncubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background 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-Pit1 antibody [EPR28191-52] - BSA and Azide free (AB313643)
This data was developed using ab313642, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human pituitary tissue labeling Pit1 with ab313642 at 1/100 (5.25 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on human pituitary (PMID : 2902927, 27351100).The section was incubated with ab313642 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrumentIncubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background 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-Pit1 antibody [EPR28191-52] - BSA and Azide free (AB313643)
This data was developed using ab313642, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded mouse liver tissue labeling Pit1 with ab313642 at 1/500 (1.05 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : no staining on mouse liver.The section was incubated with ab313642 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrumentIncubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background 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-Pit1 antibody [EPR28191-52] - BSA and Azide free (AB313643)
This data was developed using ab313642, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded rat liver tissue labeling Pit1 with ab313642 at 1/500 (1.05 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : no staining on rat liver.The section was incubated with ab313642 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrumentIncubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background 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-Pit1 antibody [EPR28191-52] - BSA and Azide free (AB313643)
This data was developed using ab313642, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse pituitary tissue labeling Pit1 with ab313642 at 1/500 (1.05 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on mouse pituitary.The section was incubated with ab313642 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrumentIncubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background 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-Pit1 antibody [EPR28191-52] - BSA and Azide free (AB313643)
This data was developed using ab313642, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Rat pituitary tissue labeling Pit1 with ab313642 at 1/500 (1.05 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on rat pituitary.The section was incubated with ab313642 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrumentIncubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background 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
- WB
Supplier Data
Western blot - Anti-Pit1 antibody [EPR28191-52] - BSA and Azide free (AB313643)
This data was developed using ab313642, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST Negative control : cerebellum (PMID : 2902927), liver (PMID : 2902927), kidney (PMID : 2902927), spleen. The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 33927188, 16968807). The identity of the higher MW band at approximately 70 kDa is unknown. In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds.
All lanes:
Western blot - Anti-Pit1 antibody [EPR28191-52] (<a href='/en-us/products/primary-antibodies/pit1-antibody-epr28191-52-ab313642'>ab313642</a>) at 1/1000 dilution
Lane 1:
Human pituitary tissue lysate at 20 µg
Lane 2:
Human cerebellum tissue lysate at 20 µg
Lane 3:
Human liver tissue lysate at 20 µg
Lane 4:
Human kidney tissue lysate at 20 µg
Lane 5:
Human spleen tissue lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 33 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-Pit1 antibody [EPR28191-52] - BSA and Azide free (AB313643)
This data was developed using ab313642, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST Negative control : liver, skeletal muscle (PMID : 2902927). The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 33927188, 16968807). In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds
All lanes:
Western blot - Anti-Pit1 antibody [EPR28191-52] (<a href='/en-us/products/primary-antibodies/pit1-antibody-epr28191-52-ab313642'>ab313642</a>) at 1/1000 dilution
Lane 1:
Rat pituitary tissue lysate at 20 µg
Lane 2:
Rat liver tissue lysate at 20 µg
Lane 3:
Rat skeletal muscle tissue lysate 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: 33 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-Pit1 antibody [EPR28191-52] - BSA and Azide free (AB313643)
This data was developed using ab313642, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST Negative control : brain (PMID : 2902927), kidney (PMID : 2902927), heart, spleen. The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 33927188, 16968807). In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds
All lanes:
Western blot - Anti-Pit1 antibody [EPR28191-52] (<a href='/en-us/products/primary-antibodies/pit1-antibody-epr28191-52-ab313642'>ab313642</a>) at 1/1000 dilution
Lane 1:
Mouse pituitary tissue lysate at 20 µg
Lane 2:
Mouse brain tissue lysate at 20 µg
Lane 3:
Mouse heart tissue lysate at 20 µg
Lane 4:
Mouse kidney tissue lysate at 20 µg
Lane 5:
Mouse spleen tissue lysate 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: 33 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-Pit1 antibody [EPR28191-52] - BSA and Azide free (AB313643)
This data was developed using ab313642, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST In Western blot, anti-His antibody (ab213204) staining at 1/5000 dilution. Anti-H3 antibody (ab176842) loading control staining at 1/100000 dilution. Exposure time : 6 seconds
All lanes:
Western blot - Anti-Pit1 antibody [EPR28191-52] (<a href='/en-us/products/primary-antibodies/pit1-antibody-epr28191-52-ab313642'>ab313642</a>) at 1/1000 dilution
Lane 1:
293T cells transfected with an empty vector containi a His-tag whole cell lysate at 20 µg
Lane 2:
293T cells transfected with a human Pit1 expression vector containi a His-tag whole cell lysate 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 1/100000 dilution
Observed band size: 33 kDa
false
Exposure time: 6s
Related conjugates and formulations (1)
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Anti-Pit1 antibody [EPR28191-52]
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.
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
The Pit1 protein regulates the transcription of genes related to hormonal production in the anterior pituitary gland. It interacts with other transcription factors to form a complex that ensures the precise regulation of target genes. This regulation is essential for normal growth metabolism and reproductive functions. By controlling the expression of growth hormone thyroid-stimulating hormone and prolactin Pit1 directly affects various physiological processes in the body.
Pathways
Pit1 plays a vital role in the growth hormone (GH) and prolactin signaling pathways. It interacts with various regulatory proteins that modulate gene expression within these pathways. In the GH pathway Pit1 collaborates with proteins like GH-releasing hormone receptor to ensure adequate hormone levels in circulation. Additionally within the prolactin pathway Pit1 ensures the proper function of Jak-STAT signaling important for reproductive and metabolic functions. Its activity impacts important pathway components and further affects energy balance and cell proliferation.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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