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Read our guarantee »Products:Cell Biology >> Apoptosis >> Receptors >> Associated Proteins
Anti-galectin 9 antibody
See all galectin 9 products (3) ...
Rabbit polyclonal to galectin 9
IHC-P, WB, ELISA, ICC/IFmore details
Reacts with
Mouse, Rat, Human
Synthetic peptide derived from the internal region of human galectin 9.
NIH/3T3 cells. Extracts from HepG2 cells.
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.02% Sodium Azide
Constituents: 50% Glycerol, PBS, 150mM Sodium chloride, pH 7.4
Concentration information loading...
Immunogen affinity purified
Polyclonal
IgG
Cell Biology >> Cell Cycle >> Cell differentiation
Neuroscience >> Cell Adhesion Proteins >> Nuclear Proteins
Cell Biology >> Apoptosis >> Receptors >> Associated Proteins
Our Abpromise guarantee covers the use of ab69630 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-P: Use a concentration of 4 µg/mlPerform heat mediated antigen retrieval before commencing with IHC staining protocol.
WB: 1/500 - 1/1000.Detects a band of approximately 40 kDa (predicted molecular weight: 40 kDa).
ELISA: 1/5000
ICC/IF: 1/500 - 1/1000.
Binds galactosides. Has high affinity for the Forssman pentasaccharide. May play a role in thymocyte-epithelial interactions relevant to the biology of the thymus. Inhibits cell proliferation. It is a ligand for HAVCR2/TIM3. Induces T-helper type 1 lymphocyte (Th1) death. Isoform Short acts as an eosinophil chemoattractant.
Peripheral blood leukocytes and lymphatic tissues. Overexpressed in Hodgkin disease tissue.
Contains 2 galectin domains.
Contains two homologous but distinct carbohydrate-binding domains.
Cytoplasm. Secreted. May also be secreted by a non-classical secretory pathway.
Target information above from: UniProt accessionO00182
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - galectin 9 antibody (ab69630)

All lanes : Anti-galectin 9 antibody (ab69630) at 1/500 dilution
Lane 1 : Extracts from HepG2 cells
Lane 2 : Extracts from HepG2 cells with immunising peptide at 5 µg
Lysates/proteins at 5 µg per lane.
Predicted band size : 40 kDa
Observed band size : 40 kDa
Immunocytochemistry/ Immunofluorescence - galectin 9 antibody (ab69630)

Immunofluorescence analysis of NIH/3T3 cells using ab69630 at 1/500 dilution, with (right panel) or without (left panel) the immunising peptide.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)-galectin 9 antibody(ab69630)

ab69360 (4µg/ml) staining Galectin 9 in human lymphoma using an automated system (DAKO Autostainer Plus). Using this protocol there is cytoplasmic and secreted staining throughout the tumour.
Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer EDTA pH 9.0 in a DAKO PT link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako envision flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
This product has been referenced in:
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All lanes : Anti-galectin 9 antibody (ab69630) at 1/500 dilution
Lane 1 : Extracts from HepG2 cells
Lane 2 : Extracts from HepG2 cells with immunising peptide at 5 µg
Lysates/proteins at 5 µg per lane.
Predicted band size : 40 kDa
Observed band size : 40 kDa

Immunofluorescence analysis of NIH/3T3 cells using ab69630 at 1/500 dilution, with (right panel) or without (left panel) the immunising peptide.

ab69360 (4µg/ml) staining Galectin 9 in human lymphoma using an automated system (DAKO Autostainer Plus). Using this protocol there is cytoplasmic and secreted staining throughout the tumour.
Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer EDTA pH 9.0 in a DAKO PT link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako envision flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
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