Anti-PAX8 抗体 [SP348] - N-terminal
Anti-PAX8 antibody [SP348] - N-terminal
- BOND RX™ Validated
- RabMAb
- Advanced Validation
- Recombinant
- 20ul selling size
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(1 Review)
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(7 Publications)
Anti-PAX8 antibody [SP348] - N-terminal (ab227707) is a rabbit monoclonal antibody detecting PAX8 in Western Blot, Flow Cytometry, IHC-P, ICC/IF, mIHC. Suitable for Human.
- Multiplex IHC validated on the Leica BOND® MAX using Opal reagents
- Biophysical QC for unrivalled batch-batch consistency
別名を表示する
Paired box protein Pax-8, PAX8
- mIHC
Lab
Multiplex immunohistochemistry - Anti-PAX8 antibody [SP348] - N-terminal (AB227707)
Fluorescence multiplex immunohistochemical analysis of Human thyroid gland tissue (Formalin/PFA-fixed paraffin-embedded sections). Panel A : merged staining of anti-Thyroglobulin (ab151539, magenta; Opal™690), anti-Thyroid Peroxidase/TPO (ab109383, green; Opal™520) and anti-PAX8 (ab227707, red; Opal™570) on human thyroid gland. Panel B : anti-Thyroid Peroxidase/TPO stained on cytoplasm of follicular epithelial cells. Panel C : anti-PAX8 stained on nucleus of follicular epithelial cells. Panel D : anti-Thyroglobulin stained on colloid. Opal Polymer HRP Ms + Rb was used as a secondary antibody. The section was incubated in three rounds of staining : in the order of ab151539 at 1/5000 dilution (0.167 μg/ml), ab109383 at 1/1500 dilution (0.072 μg/ml) , and ab227707 at 1/200 dilution (5.22 μg/ml) for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system. The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope. DAPI (blue) was used as a nuclear counter stain. Heat mediated antigen retrieval 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-PAX8 antibody [SP348] - N-terminal (AB227707)
Formalin-fixed, paraffin-embedded human uterus tissue stained for PAX8 using ab227707 at 1/100 dilution in immunohistochemical analysis.
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-PAX8 antibody [SP348] - N-terminal (AB227707)
Flow Cytometry analysis of HL-60 (human promyelocytic leukemia cell line) cells, labeling PAX8 with ab227707 at 1/100 dilution (green) compared to a Rabbit IgG negative control (blue).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PAX8 antibody [SP348] - N-terminal (AB227707)
Formalin-fixed, paraffin-embedded human thyroid tissue stained for PAX8 using ab227707 at 1/100 dilution in immunohistochemical analysis.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PAX8 antibody [SP348] - N-terminal (AB227707)
Formalin-fixed, paraffin-embedded human endometrial adenocarcinoma tissue stained for PAX8 using ab227707 at 1/100 dilution in immunohistochemical analysis.
- Flow Cyt
Unknown
Flow Cytometry - Anti-PAX8 antibody [SP348] - N-terminal (AB227707)
Flow Cytometry analysis of SK-OV-3 (human ovarian cancer epithelial cell) cells labeling PAX8 with purified ab227707 at 1 : 400 dilution (1.015 µg/ml) - Red. Cells were fixed with 4% paraformaldehyde . A Goat anti rabbit IgG (Alexa Fluor® 488, ab150081) secondary antibody was used at 1 : 2000 dilution. Isotype control - Rabbit monoclonal IgG (ab172730) - Black. Unlabeled control - Blue.
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-PAX8 antibody [SP348] - N-terminal (AB227707)
Immunocytochemistry/ Immunofluorescence analysis of SK-OV-3 (human ovarian cancer epithelial cell) cells labeling PAX8 with purified ab227707 at 1 : 50 (8.1 µg/ml). Cells were fixed in 4% paraformaldehyde and permeabilized with 0.1% Triton X-100. Cells were counterstained with ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) 1 : 200 (2.5 µg/ml). Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) was used as the secondary antibody at 1 : 1000 (2 µg/ml) dilution. DAPI nuclear counterstain. PBS instead of the primary antibody was used as the secondary antibody only control.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PAX8 antibody [SP348] - N-terminal (AB227707)
Formalin-fixed, paraffin-embedded human kidney tissue stained for PAX8 using ab227707 at 1/100 dilution in immunohistochemical analysis.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PAX8 antibody [SP348] - N-terminal (AB227707)
Formalin-fixed, paraffin-embedded human tonsil tissue stained for PAX8 using ab227707 at 1/100 dilution in immunohistochemical analysis.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PAX8 antibody [SP348] - N-terminal (AB227707)
Formalin-fixed, paraffin-embedded human ovarian adenocarcinoma tissue stained for PAX8 using ab227707 at 1/100 dilution in immunohistochemical analysis.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PAX8 antibody [SP348] - N-terminal (AB227707)
Formalin-fixed, paraffin-embedded human fallopian tube tissue stained for PAX8 using ab227707 at 1/100 dilution in immunohistochemical analysis.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PAX8 antibody [SP348] - N-terminal (AB227707)
Formalin-fixed, paraffin-embedded human renal cell carcinoma tissue stained for PAX8 using ab227707 at 1/100 dilution in immunohistochemical analysis.
- ChIC/CUT&RUN-seq
Lab
ChIC/CUT&RUN sequencing - Anti-PAX8 antibody [SP348] - N-terminal (AB227707)
ChIC/CUT&RUN was performed using a pAG-MNase at a final concentration of 700 ng/mL, 2.5 x 10^5 NIH : OVCAR-3 (Human ovary adenocarcinoma epithelial cell) cells and 5 µg of ab227707 [SP348]. The resulting DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 10 million reads. The negative IgG control ab172730 is also shown. The University of Geneva owns patents relevant to ChIC (Chromatin Immuno-Cleavage) methods."
- ChIC/CUT&RUN-seq
Lab
ChIC/CUT&RUN sequencing - Anti-PAX8 antibody [SP348] - N-terminal (AB227707)
ChIC/CUT&RUN was performed using a pAG-MNase at a final concentration of 700 ng/mL, 2.5 x 10^5 NIH : OVCAR-3 (Human ovary adenocarcinoma epithelial cell) cells and 5 µg of ab227707 [SP348]. The resulting DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 10 million reads. The negative IgG control ab172730 is also shown. The University of Geneva owns patents relevant to ChIC (Chromatin Immuno-Cleavage) methods."
- ChIC/CUT&RUN-seq
Lab
ChIC/CUT&RUN sequencing - Anti-PAX8 antibody [SP348] - N-terminal (AB227707)
ChIC/CUT&RUN was performed using a pAG-MNase at a final concentration of 700 ng/mL, 2.5 x 10^5 NIH : OVCAR-3 (Human ovary adenocarcinoma epithelial cell) cells and 5 µg of ab227707 [SP348]. The resulting DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 10 million reads. The negative IgG control ab172730 is also shown. The University of Geneva owns patents relevant to ChIC (Chromatin Immuno-Cleavage) methods."
- WB
Lab
Western blot - Anti-PAX8 antibody [SP348] - N-terminal (AB227707)
All lanes:
Western blot - Anti-PAX8 antibody [SP348] - N-terminal (ab227707) at 0.398 µg/mL
Lane 1:
SK-OV-3 (human ovarian cancer epithelial cell) cell lysate at 20 µg
Lane 2:
human kidney tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 0.05 µg/mL
Predicted band size: 48 kDa
false
- WB
Supplier Data
Western blot - Anti-PAX8 antibody [SP348] - N-terminal (AB227707)
All lanes:
Western blot - Anti-PAX8 antibody [SP348] - N-terminal (ab227707) at 1/100 dilution
Lane 1:
PAX1 transfected HEK-293 (human epithelial cel line from embryonic kidney) cell lysate
Lane 2:
PAX2 transfected HEK-293 (human epithelial cel line from embryonic kidney) cell lysate
Lane 3:
PAX3 transfected HEK-293 (human epithelial cel line from embryonic kidney) cell lysate
Lane 4:
PAX4 transfected HEK-293 (human epithelial cel line from embryonic kidney) cell lysate
Lane 5:
PAX5 transfected HEK-293 (human epithelial cel line from embryonic kidney) cell lysate
Lane 6:
PAX6 transfected HEK-293 (human epithelial cel line from embryonic kidney) cell lysate
Lane 7:
PAX7 transfected HEK-293 (human epithelial cel line from embryonic kidney) cell lysate
Lane 8:
PAX8 transfected HEK-293 (human epithelial cel line from embryonic kidney) cell lysate
Lane 9:
PAX9 transfected HEK-293 (human epithelial cel line from embryonic kidney) cell lysate
Lane 10:
Mock transfected HEK-293 (human epithelial cel line from embryonic kidney) cell lysate
Predicted band size: 48 kDa
false
関連する標識済み抗体及び組成の異なる製品 (2)
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Anti-PAX8 antibody [SP348] - BSA and Azide free
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-PAX8 - N-terminal antibody [SP348]
Reactivity data
製品の詳細
Abcam's high quality manufacturing and validation processes ensure Anti-PAX8 antibody [SP348] - N-terminal (ab227707) has high sensitivity and specificity alongside high lot-to-lot consistency and reproducibility.
Anti-PAX8 antibody [SP348] - N-terminal (ab227707) specifically detects PAX8 (UniProt ID: Q06710; Molecular weight: 49kDa) and is sold in 100 µL, 500 µL and 1 mL selling sizes.
Conjugation-ready, carrier free format available for antibody clone SP348 - ab242429.
Antibody clone SP348 is also available pre-conjugated to a variety of labels for your convenience - Alexa Fluor® 647 (ab313345).
Anti-PAX8 antibody [SP348] - N-terminal (ab227707) is a clone from the portfolio of Spring Bioscience (Roche) SP clones which have been optimised for immunohistochemistry (IHC).
Highly-specific to PAX8. Western blotting data to guarantee specificity to PAX8 with no cross-reactivity with other PAX family members. Validated for CUT&RUN-seq, a key application to map protein-DNA interactions on a genome-wide scale using NGS. A highly-validated antibody for studying PAX8 as a transcription factor, its role in thyroid and renal cancers and epigenetic regulation. This antibody is crucial in cancer research, particularly in understanding PAX8's involvement in tumorigenesis and gene expression and is widely used in studies of embryogenesis and cancers of the Mьllerian duct.
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補足情報
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The PAX8 protein regulates the expression of genes related to organogenesis and cell fate determination. It forms part of transcriptional regulatory complexes partnering with other proteins to modulate gene activity. PAX8 supports embryonic development especially in the thyroid and urogenital tract. Its presence ensures the proper function and formation of these organs highlighting its significance in developmental biology.
Pathways
PAX8 interacts with several key biological processes. It notably participates in the thyroid hormone synthesis pathway where it regulates the expression of thyroglobulin and thyroperoxidase. PAX8 also affects the renal system through its interaction with WT1 a protein involved in kidney development. These pathways illustrate PAX8's role in maintaining endocrine and renal functions by influencing important protein interactions.
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文献 (7)
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