ARHGAP29 Antibody is a premium polyclonal that offers outstanding performance and reliability for demanding research applications. Rigorously validated for ELISA, this antibody ensures consistent, reproducible results across multiple experimental platforms. Demonstrates excellent reactivity with Human samples, providing researchers with confidence in cross-species compatibility. Conveniently packaged in 50ug format to meet your experimental needs. For optimal performance, store at -20°C or -80°C and maintains stability for 12 months. Backed by rigorous quality control testing to ensure superior performance in your critical research applications.
Product Name:
ARHGAP29 Antibody (PACO36082)
SKU:
PACO36082
Size:
50μg
Isotype:
IgG
Host Species:
Rabbit
Reactivity:
Human
Immunogen:
Recombinant Human Rho GTPase-activating protein 29 protein (161-392AA)
Immunogen Species:
Homo sapiens (Human)
Uniprot No:
Q52LW3
Form:
Liquid
Tested Applications:
ELISAIHCIF
Recommended Dilution:
IHC 1:100-1:200, IF 1:50-1:150
Synonyms:
ARHGAP 29 antibody, Arhgap29 antibody, ARHGAP29 protein antibody, MGC166097 antibody, PARG 1 antibody, PARG1 antibody, PTPL1 associated RhoGAP 1 antibody, PTPL1-associated RhoGAP protein 1 antibody, RHG29_HUMAN antibody, Rho GTPase activating protein 29 antibody, Rho GTPase activating protein 29 isoform CRA_a antibody, Rho GTPase activating protein 29 isoform CRA_b antibody, Rho GTPase-activating protein 29 antibody, Rho-type GTPase-activating protein 29 antibody
IHC image of PACO36082 diluted at 1:200 and staining in paraffin-embedded mouse kidney tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB. Secondary antibody only control: uses 1% BSA instead of primary antibody
Immunofluorescence staining of U251 cell with PACO36082 at 1:130, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).
Immunofluorescence staining of U251 cell with 5% goat serum, counter-stained with DAPI. TheCcells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).
Immunofluorescence staining of A431 cell with PACO36082 at 1:130, counter-stained with DAPI. TheCcells wereCfixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).
Immunofluorescence staining of U251 cell with PACO36082 at 1:130, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).
