product summary
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company name :
HUABIO
product type :
antibody
product name :
Anti-PAX5 Antibody [JJ08-87]
catalog :
ET1701-49TR
quantity :
20 uL
price :
99 USD
clonality :
monoclonal
host :
domestic rabbit
conjugate :
nonconjugated
clone name :
JJ08-87
reactivity :
human, mouse
application :
western blot, flow cytometry, immunohistochemistry - paraffin section
more info or order :
product information
SKU :
ET1701-49TR
Target name :
Anti-PAX5 Antibody [JJ08-87]
Species reactivity :
Human,Mouse
Applications :
WB,IF-Cell,IF-Tissue,IHC-P,FC
Conjugate :
Non-conjugated
Immunogen :
Synthetic peptide within human PAX5 aa 240-280.
Uniprot id :
SwissProt: Q02548 Human;SwissProt: Q02650 Mouse
Host :
Rabbit
Clone number :
JJ08-87
Isotype :
IgG
Size :
20 uL
List Price :
99 USD
Storage Buffer :
1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Form :
Liquid
Storage Instruction :
Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles.
Purity :
Protein A affinity purified.
Product type :
Recombinant Rabbit monoclonal Antibody
Positive control :
Ramos cell lysate, Raji cell lysate, Daudi cell lysates, Hela, MCF-7, HepG2, human lymph nodes tissue, human tonsil tissue, human spleen tissue, Raji.
Molecular wt :
Predicted band size: 42 kDa
Subcellular location :
Nucleus.
Concentration :
1 mg/mL.
Recommended dilutions :
WB: 1:5,000
;IF-Cell: 1:50-1:200
;IF-Tissue: 1:50-1:200
;IHC-P: 1:400-1:1,000
;FC: 1:50-1:100
Pic img4 :
ET1701-49_2.jpg
Pic img5 :
ICC staining of PAX5 in Hela cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1701-49, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
Pic legend5 :
ET1701-49_3.jpg
Pic legend6 :
ICC staining of PAX5 in MCF-7 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1701-49, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
Pic img7 :
ET1701-49_4.jpg
Pic img8 :
ICC staining of PAX5 in HepG2 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1701-49, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
Pic legend8 :
ET1701-49_5.jpg
Pic legend9 :
Immunohistochemical analysis of paraffin-embedded human lymph nodes tissue with Rabbit anti-PAX5 antibody (ET1701-49) at 1/1,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1701-49) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Pic img10 :
ET1701-49_6.jpg
Pic img11 :
Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Rabbit anti-PAX5 antibody (ET1701-49) at 1/1,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1701-49) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Pic legend11 :
ET1701-49_7.jpg
Pic legend12 :
Immunohistochemical analysis of paraffin-embedded human spleen tissue with Rabbit anti-PAX5 antibody (ET1701-49) at 1/400 dilution.
The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1701-49) at 1/400 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Pic img13 :
ET1701-49_8.jpg
Pic img14 :
Flow cytometric analysis of PAX5 was done on Raji cells. The cells were fixed, permeabilized and stained with the primary antibody (ET1701-49, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
more info or order :
company information

HUABIO
Founded in 2007, HUABIO is dedicated to developing high-quality antibodies that advance innovation. We are passionate about the accuracy, efficiency, and consistency of our products. That is why we have invested in new production platforms, like recombinant rabbit monoclonals, alpaca nanobodies, and adopted aggressive QA standards to deliver cutting-edge antibodies with uncompromised quality.
We hope to see you at your next discovery!
We hope to see you at your next discovery!
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