This antibody recognizes an extracellular epitope of human SIGLEC10, a sialic acid-binding lectin expressed on subsets of human leucocytes.
Applications
Flow Cytometry
Dilutions
Flow Cytometry: The reagent is designed for analysis of human blood cells using 10 µl reagent / 100 µl of whole blood or 106 cells in a suspension. The content of a vial (1 ml) is sufficient for 100 tests.
Reactivity
Human
Immunogen
SIGLEC10 extracellular domain fused with human IgG1 Fc fragment.
Host
Mouse
Clonality
Monoclonal
Clone ID
5G6
Isotype
IgG1
Conjugate
PE
Excitation: 565nm, Emission: 578nm
Purification
This antibody is conjugated with R-phycoerythrin (PE) under optimum conditions. The conjugate is purified by size-exclusion chromatography; removing unconjugated antibody and free fluorochrome.
Product Form
Liquid
Formulation
Supplied in Phosphate Buffered Saline, pH 7.4, with 15 mM Sodium Azide.
Storage
Shipped at 4°C. Store in the dark at 2-8°C. Do not freeze!
Synonyms
Sialic acid-binding Ig-like lectin 10, Siglec-10, Siglec-like protein 2, SLG2
Anti-SIGLEC10 Antibody [5G6] (PE) (A320788) works in flow cytometry application. Analysis of the antibody staining profile was performed on blood leukocytes isolated from buffy coats. HCDM CDMaps standardized procedures were used for cell isolation and surface staining of blood leukocytes, with the modification of staining protocol using cytometry test tubes. Mouse monoclonal anti-human SIGLEC10 PE antibody (clone 5G6) was used in amount of 10 µl in 100 µl of blood sample (2 x 106 cells).
Expression profiling on peripheral blood subsets using Anti-SIGLEC10 Antibody [5G6] (PE) (A320788). HCDM CDMaps standardized procedures were used for cell isolation and surface staining of blood leukocytes, with the modification of staining protocol using cytometry test tubes. Suspension of blood leukocytes isolated from buffy coats (2 x 106 cells) was added to the mixture of anti-human SIGLEC10 PE antibody (clone 5G6, 10 µl reagent / 100 µl of stained blood sample) and Monocyte Blocking Buffer (#ED7747), vortexed and incubated for 20 min. Next, optimized backbone antibody panels (HLDA Innate and HLDA Adaptive) were added to test tubes, vortexed and incubated for 20 min. The residual erythrocytes were lysed with 2 ml of 10× diluted EXCELLYSE Easy solution (#ED7066) and incubated for 10 min. Finally, samples were centrifuged (670 g, 5 min.), supernatant removed and the cell pellet was resuspended in 200 µl of PBS for acquisition.
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Proteins predicted to interact with SIGLEC10
Predicted protein interactions based upon String database. Revelancy score correlates with probability of interaction.