Anti-PAX7 antibody [EPR30466-531]
- BOND RX™ Validated
- RabMAb
- Recombinant
- 20ul selling size
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Rabbit Recombinant Monoclonal PAX7 antibody. Suitable for IHC-P, WB, ICC/IF and reacts with Transfected cell line - Mouse, Mouse, Human samples.
View Alternative Names
Pax-7, Paired box protein Pax-7
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-PAX7 antibody [EPR30466-531] (AB324017)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized TT (human thyroid carcinoma epithelial cell) cells labelling PAX7 with ab324017 at 1/500 (0.994 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2ug/ml) dilution (Green).
Confocal image showing nuclear staining in TT cell line (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue).
Low expression : HeLa.
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 (2.5ug/ml) dilution (Magenta).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2ug/ml) dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PAX7 antibody [EPR30466-531] (AB324017)
Immunohistochemical analysis of paraffin-embedded (A) HEK-293T (human embryonic kidney epithelial cell) transfected with a Mouse Pax7 expression vector containing a Myc-His tag and (B) HEK-293T transfected with empty vector containing a Myc-His tag labeling PAX7 with ab324017 at 1/2000 (0.249 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining in (A) HEK-293T (human embryonic kidney epithelial cell) transfected with a Mouse Pax7 expression vector containing a Myc-His tag, no signal in (B) HEK-293T transfected with empty vector containing a Myc-His tag.
The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
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-PAX7 antibody [EPR30466-531] (AB324017)
Immunohistochemical analysis of paraffin-embedded Mouse E12.5 brain tissue labeling PAX7 with ab324017 at 1/2000 (0.249 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse E12.5 brain.
The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
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-PAX7 antibody [EPR30466-531] (AB324017)
Immunohistochemical analysis of paraffin-embedded (A) C2C12 (mouse myoblast) cell pellets; (B) NIH/3T3 (mouse embryonic fibroblast) cell pellets labeling PAX7 with ab324017 at 1/2000 (0.249 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining in (A) C2C12 (mouse myoblast) cell pellets, no signal in (B) NIH/3T3 (mouse embryonic fibroblast) cell pellets.
The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
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-PAX7 antibody [EPR30466-531] (AB324017)
Immunohistochemical analysis of paraffin-embedded Mouse testis tissue labeling PAX7 with ab324017 at 1/2000 (0.249 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : No staining in mouse testis (PMID : 25133429).
The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
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-PAX7 antibody [EPR30466-531] (AB324017)
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling PAX7 with ab324017 at 1/2000 (0.249 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining in mouse cerebrum.
The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
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-PAX7 antibody [EPR30466-531] (AB324017)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Negative control : HeLa (PMID : 11030621).
To minimize protein degradation, cells were lysed immediately after harvest and then applied to a gel and transfer membrane for Western blotting as soon as possible.
In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution.
All lanes:
Western blot - Anti-PAX7 antibody [EPR30466-531] (ab324017) at 1/1000 dilution
Lane 1:
TT (human thyroid carcinoma epithelial cell) whole cell lysate at 60 µg
Lane 2:
HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate at 60 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: 54 kDa,124 kDa
false
Exposure time: 6s
- WB
Supplier Data
Western blot - Anti-PAX7 antibody [EPR30466-531] (AB324017)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Negative control : mouse kidney (PMID : 11030621).
To minimize protein degradation, tissues were lysed immediately after harvest and then applied to a gel and transfer membrane for Western blotting as soon as possible.
In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution.
All lanes:
Western blot - Anti-PAX7 antibody [EPR30466-531] (ab324017) at 1/1000 dilution
Lane 1:
Mouse E12-E14.5 brain tissue lysate at 20 µg
Lane 2:
Mouse kidney 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: 54 kDa,124 kDa
false
Exposure time: 48s
- WB
Supplier Data
Western blot - Anti-PAX7 antibody [EPR30466-531] (AB324017)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Negative control : mouse testis (PMID : 25133429)
To minimize protein degradation, tissues were lysed immediately after harvest and then applied to a gel and transfer membrane for Western blotting as soon as possible.
In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution.
All lanes:
Western blot - Anti-PAX7 antibody [EPR30466-531] (ab324017) at 1/1000 dilution
Lane 1:
Mouse E12 embryo tissue lysate at 60 µg
Lane 2:
Mouse E15 brain tissue lysate at 60 µg
Lane 3:
Mouse testis tissue lysate at 60 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: 54 kDa,124 kDa
false
Exposure time: 26s
- WB
Supplier Data
Western blot - Anti-PAX7 antibody [EPR30466-531] (AB324017)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Negative control : NIH/3T3 (PMID : 11030621).
To minimize protein degradation, cells were lysed immediately after harvest and then applied to a gel and transfer membrane for Western blotting as soon as possible.
In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution.
All lanes:
Western blot - Anti-PAX7 antibody [EPR30466-531] (ab324017) at 1/1000 dilution
Lane 1:
C2C12 (mouse myoblast) whole cell lysate at 20 µg
Lane 2:
NIH/3T3 (mouse embryonic fibroblast) 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 1/20000 dilution
Observed band size: 54 kDa,124 kDa
false
Exposure time: 81s
- WB
Supplier Data
Western blot - Anti-PAX7 antibody [EPR30466-531] (AB324017)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
To minimize protein degradation, cells were lysed immediately after harvest and then applied to a gel and transfer membrane for Western blotting as soon as possible.
In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution.
All lanes:
Western blot - Anti-PAX7 antibody [EPR30466-531] (ab324017) at 1/1000 dilution
Lane 1:
C2C12 (mouse myoblast) transfected with scrambled siRNA control whole cell lysate at 20 µg
Lane 2:
C2C12 transfected with siRNA specifically targeting PAX7 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 1/20000 dilution
Observed band size: 54 kDa,124 kDa
false
Exposure time: 95s
Related conjugates and formulations (1)
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Anti-PAX7 antibody [EPR30466-531] - 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
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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
Product protocols
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Target data
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Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com