LMO7 Antibody is a premium polyclonal that offers outstanding performance and reliability for demanding research applications. Rigorously validated for ELISA, IHC, IF, 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:
LMO7 Antibody
SKU:
PACO60236
Size:
50μg
Isotype:
IgG
Host Species:
Rabbit
Reactivity:
Human
Immunogen:
Recombinant Human LIM domain only protein 7 protein (1301-1465AA)
Immunogen Species:
Homo sapiens (Human)
Uniprot No:
Q8WWI1
Form:
Liquid
Tested Applications:
ELISAIHCIF
Recommended Dilution:
Application
Recommended Dilution
IHC
1:200-1:500
IF
1:50-1:200
Synonyms:
F box only protein 20 antibody, F box protein Fbx20 antibody, F-box only protein 20 antibody, FBX20 antibody, FBXO20 antibody, HGNC13591 antibody, KIAA0858 antibody, LIM domain only 7 antibody, LIM domain only protein 7 antibody, LMO 7 antibody, LMO-7 antibody, LMO7 antibody, LMO7_HUMAN antibody, LOMP antibody, LOMP protein antibody, Zinc finger domain containing protein antibody
IHC image of PACO60236 diluted at 1:200 and staining in paraffin-embedded human appendix 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 biotinylated secondary antibody and visualized using an HRP conjugated SP system.
IHC image of PACO60236 diluted at 1:200 and staining in paraffin-embedded human colon cancer 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 biotinylated secondary antibody and visualized using an HRP conjugated SP system.
Immunofluorescence staining of Hela cells with PACO60236 at 1:66, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).
