SLC30A10 Antibody is a premium polyclonal that offers outstanding performance and reliability for demanding research applications. Rigorously validated for ELISA, WB, IHC, IF, this antibody ensures consistent, reproducible results across multiple experimental platforms. Demonstrates excellent reactivity with Human, Mouse 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:
SLC30A10 Antibody
SKU:
PACO46666
Size:
50μg
Isotype:
IgG
Host Species:
Rabbit
Reactivity:
Human, Mouse
Immunogen:
Recombinant Human Zinc transporter 10 protein (58-278AA)
Immunogen Species:
Homo sapiens (Human)
Uniprot No:
Q6XR72
Form:
Liquid
Tested Applications:
ELISAWBIHC
Recommended Dilution:
Application
Recommended Dilution
WB
1:500-1:2000
IHC
1:50-1:200
Synonyms:
SLC30A10, ZNT10, ZNT8, Zinc transporter 10, ZnT-10, Manganese transporter SLC30A10, Solute carrier family 30 member 10
Western Blot Positive WB detected in: SY5Y whole cell lysate(20µg), COLO205 whole cell lysate(20µg), Mouse Brain tissue lysate(20µg) All lanes: SLC30A10 antibody at 1:1000 Secondary Goat polyclonal to rabbit IgG at 1/20000 dilution Predicted band size: 53,27,25 kDa Observed band size: 53 kDa Exposure time: 120s
IHC image of PACO46666 diluted at 1:50 and staining in paraffin-embedded human liver 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
IHC image of PACO46666 diluted at 1:50 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 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
