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Anti-Ki67 Antibody CQA9285
  • Western blot analysis of Ki67 expression in whole cell lysates.
  • Immunohistochemical analysis of Ki67 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-Ki67 Antibody
Cat No: CQA9285
Source: Mouse
Reactivity: H
Applications: 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 Ki67
Immunogen: KLH-conjugated synthetic peptide encompassing a sequence within the center region of human Ki67. The exact sequence is proprietary.
Purification: This antibody is purified through a protein G column.
Clonality: Monoclonal
Form: Mouse IgG1. Liquid in PBS, pH 7.3, 30% glycerol, and 0.01% sodium azide.
Dilution: IH (1/50 - 1/200)
Gene Symbol: MKI67
Alternative Names: Antigen KI-67
Entrez Gene (Human): 4288
SwissProt (Human): P46013
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 Ki67 expression in whole cell lysates.
  • Immunohistochemical analysis of Ki67 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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