LGI4 Antibody is a premium polyclonal that offers outstanding performance and reliability for demanding research applications. Rigorously validated for ELISA, IHC, 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:
LGI4 Antibody (PACO58288)
SKU:
PACO58288
Size:
50μg
Isotype:
IgG
Host Species:
Rabbit
Reactivity:
Human
Immunogen:
Recombinant Human Leucine-rich repeat LGI family member 4 protein (292-412AA)
Immunogen Species:
Homo sapiens (Human)
Uniprot No:
Q8N135
Form:
Liquid
Tested Applications:
ELISAIHC
Recommended Dilution:
IHC 1:200-1:500
Synonyms:
Leucine rich glioma inactivated gene 4 antibody, Leucine rich glioma inactivated protein 4 antibody, Leucine rich repeat LGI family member 4 antibody, Leucine-rich glioma-inactivated protein 4 antibody, Leucine-rich repeat LGI family member 4 antibody, LGI1 like protein 3 antibody, LGI1-like protein 3 antibody, LGI4 antibody, Lgi4 protein antibody, LGI4_HUMAN antibody, Lgil3 antibody
IHC image of PACO58288 diluted at 1:200 and staining in paraffin-embedded human lung 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.
IHC image of PACO58288 diluted at 1:200 and staining in paraffin-embedded human liver 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.
