Anti-PAX7 antibody ab187339 is a rabbit polyclonal antibody that is used in PAX7 western blotting and immunofluorescence. Suitable for human and mouse samples.
IgG
Rabbit
Preservative: 0.05% Sodium azide
Constituents: 69% PBS, 30% Glycerol (glycerin, glycerine), 0.1% BSA
Liquid
Polyclonal
ICC/IF | IP | WB | |
---|---|---|---|
Human | Tested | Tested | Tested |
Mouse | Tested | Expected | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/20.00000 - 1/200.00000 | Notes - |
Species Human | Dilution info 1/20.00000 - 1/200.00000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 3 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/1000.00000 - 1/2000.00000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info Use at an assay dependent concentration. | Notes - |
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Transcription factor that is involved in the regulation of muscle stem cells proliferation, playing a role in myogenesis and muscle regeneration.
HUP1, HUP1, PAX7, Paired box protein Pax-7, HuP1
Anti-PAX7 antibody ab187339 is a rabbit polyclonal antibody that is used in PAX7 western blotting and immunofluorescence. Suitable for human and mouse samples.
IgG
Rabbit
Preservative: 0.05% Sodium azide
Constituents: 69% PBS, 30% Glycerol (glycerin, glycerine), 0.1% BSA
Liquid
Polyclonal
Affinity purification Immunogen
Western blot analysis of ab187339 detects a prominent ~54 kDa protein in human HeLa, MCF7, rhabdomyosarcoma and skeletal muscle satellite cells and a weaker ~57 kDa protein in HeLa, rhabdomyosarcoma and skeletal muscle satellite cells. The ~57 kDa band seems to be enriched in immunoprecipitations from HeLa lysate, suggesting a bias for the larger isoform in ths application.
Blue Ice
1-2 weeks
+4°C
-20°C
Upon delivery aliquot
Avoid freeze / thaw cycle
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This supplementary information is collated from multiple sources and compiled automatically.
PAX7 or paired box 7 is a member of the paired box (PAX) family of transcription factors. Alternative names for PAX7 include PAX7 protein and PAX7 FACS. This protein has a molecular weight of approximately 57 kDa. PAX7 is mainly expressed in muscle precursor cells where it plays an important role in regulating muscle development. Researchers commonly detect it through PAX7 staining techniques in laboratory settings.
PAX7 functions are important for muscle cell proliferation and differentiation. It works within a transcriptional complex where it partners with other proteins to promote satellite cell maintenance. Satellite cells are essential for muscle regeneration and PAX7 regulates their self-renewal and differentiation. The protein also modulates various genetic targets that affect the muscle cellular environment ensuring proper muscle function and repair.
PAX7 is involved in the myogenic regulatory pathways that guide muscle development and regeneration. It interacts with important proteins like MyoD and Myf5 to influence these processes. These pathways facilitate the conversion of satellite cells into mature muscle fibers important during muscle growth and healing. PAX7’s function in these pathways ensures satellite cells remain active and capable of muscle repair throughout an organism's life.
PAX7’s dysfunction can lead to muscle-related conditions such as rhabdomyosarcoma and certain muscle dystrophies. In rhabdomyosarcoma improper regulation of PAX7 leads to unchecked cellular proliferation contributing to tumor growth. This disorder links PAX7 to other proteins in the tumorigenic pathway such as PAX3 which similarly influences muscle cell behavior in pathological states. Identifying PAX7 alterations can guide diagnosis and therapeutic strategies in muscle-associated disorders.
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Immunocytochemistry analysis of formalin-fixed HeLa cells permeabilized with 0.1% Triton X-100 staining PAX-7 in the nucleus with ab187339 in a 1/100 dilution (green). Secondary was DyLight-conjugated secondary antibody. Negative control (left), had no primary antibody. F-actin was stianed with fluorescent red phalloidin, and nuclei were stained with DAPI or Hoechst.
Immunocytochemistry analysis of formalin-fixed MCF-7 cells (human breast adenocarcinoma cell line) permeabilized with 0.1% Triton X-100 staining PAX-7 in the nucleus with ab187339 in a 1/100 dilution (green). Secondary was DyLight-conjugated secondary antibody. Negative control (left), had no primary antibody. F-actin was stianed with fluorescent red phalloidin, and nuclei were stained with DAPI or Hoechst.
Immunocytochemistry analysis of formalin-fixed C2C12 cells (mouse myoblast cell line) permeabilized with 0.1% Triton X-100 staining PAX-7 in the nucleus with ab187339 in a 1/100 dilution (green). Secondary was DyLight-conjugated secondary antibody. Negative control (left), had no primary antibody. F-actin was stianed with fluorescent red phalloidin, and nuclei were stained with DAPI or Hoechst.
All lanes: Western blot - Anti-PAX7 antibody (ab187339) at 1/1000 dilution
Lane 1: HeLa lysate transfected with empty vector control at 50 µg
Lane 2: HeLa lysate overexpressing PAX7 at 50 µg
All lanes: Goat anti-rabbit HRP at 1/20000 dilution
Developed using the ECL technique.
Predicted band size: 56 kDa
All lanes: Western blot - Anti-PAX7 antibody (ab187339) at 1/1000 dilution
Lane 1: HeLa whole cell lysate at 50 µg
Lane 2: MCF7 whole cell lysate at 50 µg
Lane 3: HSkMSC whole cell lysate at 50 µg
Lane 4: SJCRH30 whole cell lysate at 50 µg
All lanes: Goat anti-rabbit HRP at 1/20000 dilution
Developed using the ECL technique.
Predicted band size: 56 kDa
Immunoprecipitation of PAX7 was performed using HeLa whole cell lysate. Antigen-antibody complexes were formed by incubating 500μg of lysate with 3μg of ab187339 overnight on a rocking platform at 4°C. The immune complexes were captured on 50ul Protein A/G Agarose, washed extensively, and eluted. Samples was resolved on a 4-20% Tris-HCl polyacrylamide gel, transferred to a PVDF membrane, and blocked with 5% BSA/TBS-0.1%Tween-20 for 1 hour. The membrane was probed with ab187339 at 1/1000 dilution overnight rotating at 4°C.
All lanes: Immunoprecipitation - Anti-PAX7 antibody (ab187339)
Developed using the ECL technique.
Predicted band size: 56 kDa
Immunofluorescent analysis of PAX7 in MCF7 (left panel) and HeLa (right panel) cells. Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature. Cells were probed with a ab187339 at 1/100 dilution for at least 1 hour at room temperature, washed with PBS, and incubated with a DyLight 488-conjugated goat anti-rabbit IgG secondary antibody at 1/400 dilution for 30 minutes at room temperature. F-Actin (red) was stained with DyLight-554 Phalloidin and nuclei (blue) were stained with Hoechst 33342 dye.
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