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Anti-NANOG Antibody CQA9507
  • Western blot analysis of NANOG expression in Caco2 (A), MCF7 (B) whole cell lysates.
  • Immunohistochemical analysis of NANOG staining in human testis 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-NANOG Antibody
Cat No: CQA9507
Source: Mouse
Reactivity: H
Applications: WB, IH
*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
50 μl
$150
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Description: Mouse monoclonal antibody to NANOG
Immunogen: Recombinant fusion protein of human NANOG. The exact sequence is proprietary.
Purification: This antibody is purified through a protein G column.
Clonality: Monoclonal
Form: Mouse IgG1 kappa. Liquid in PBS, pH 7.3, 30% glycerol, and 0.01% sodium azide.
Dilution: WB (1/1000 - 1/2000), IH (1/50 - 1/200)
Gene Symbol: NANOG
Alternative Names: Homeobox protein NANOG; Homeobox transcription factor Nanog; hNanog
Entrez Gene (Human): 79923
SwissProt (Human): Q9H9S0
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 NANOG expression in Caco2 (A), MCF7 (B) whole cell lysates.
  • Immunohistochemical analysis of NANOG staining in human testis 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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