ENOSF1 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:
ENOSF1 Antibody (PACO58204)
SKU:
PACO58204
Size:
50μg
Isotype:
IgG
Host Species:
Rabbit
Reactivity:
Human
Immunogen:
Recombinant Human Mitochondrial enolase superfamily member 1 protein (171-286AA)
Immunogen Species:
Homo sapiens (Human)
Uniprot No:
Q7L5Y1
Form:
Liquid
Tested Applications:
ELISAIHC
Recommended Dilution:
IHC 1:200-1:500
Synonyms:
Antisense RNA to thymidylate synthase antibody, ENOF1_HUMAN antibody, Enolase superfamily member 1 antibody, ENOSF 1 antibody, enosf1 antibody, HSRTSBETA antibody, Mitochondrial enolase superfamily member 1 antibody, RTS alpha antibody, RTS antibody, RTS beta antibody, RTS beta protein antibody, TYMSAS antibody
IHC image of PACO58204 diluted at 1:200 and staining in paraffin-embedded human endometrial 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 PACO58204 diluted at 1:200 and staining in paraffin-embedded human 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 biotinylated secondary antibody and visualized using an HRP conjugated SP system.
