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Anti-IL-26 Antibody CQA8193
  • Western blot analysis of IL-26 expression in Hela (A), A549 (B), HL60 (C), U251 (D) whole cell lysates.
  • Immunohistochemical analysis of IL-26 staining in human tonsil formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
Product NameAnti-IL-26 Antibody
Cat No: CQA8193
Source: Rabbit
Reactivity: H
Applications: WB, IH, IP
*Application Key:
E- ELISA, WB - Western blot, IH - Immunohistochemistry, IF - Immunofluorescence, FC - Flow cytometry, IC - Immunocytochemistry, IP - Immunoprecipitation, ChIP - Chromatin Immunoprecipitation, EMSA - Electrophoretic Mobility Shift Assay, BL - Blocking, SE - Sandwich ELISA, CBE - Cell-based ELISA, RNAi - RNA interference
*Species Reactivity Key:
H - Human, M - Mouse, R - Rat, B - Bovine, C - Chicken, D - Dog, G - Goat, Mk - Monkey, P - Pig, Rb - Rabbit, S - Sheep, Z - Zebrafish
Size
Price
200 μl
$350
100 μl
$220
30 μl
$110
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Description: Rabbit monoclonal antibody to IL-26
Immunogen: A synthetic peptide of human IL-26
Purification: The antibody was purified by immunogen affinity chromatography.
Clonality: Monoclonal
Form: Liquid in 50mM Tris-Glycine (pH 7.4), 0.15M NaCl, 50% Glycerol, 0.01% Sodium azide and 0.05% BSA.
Dilution: WB (1/500 - 1/1000), IH (1/50 - 1/100), IP (1/10 - 1/50)
Gene Symbol: IL26
Alternative Names: AK155; Interleukin-26; IL-26; Protein AK155
Entrez Gene (Human): 55801
SwissProt (Human): Q9NPH9
Storage/Stability : Shipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.
  • Western blot analysis of IL-26 expression in Hela (A), A549 (B), HL60 (C), U251 (D) whole cell lysates.
  • Immunohistochemical analysis of IL-26 staining in human tonsil formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
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