Description: Rabbit polyclonal antibody to Collagen 11 alpha 1 Immunogen: KLH-conjugated synthetic peptide encompassing a sequence within the center region of human Collagen 11 alpha 1. The exact sequence is proprietary. Purification: The antibody was purified by immunogen affinity chromatography. Clonality: Polyclonal Form: Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide. Dilution: WB (1/500 - 1/1000), IH (1/100 - 1/200), IF/IC (1/100 - 1/500) Gene Symbol: COL11A1 Alternative Names: COLL6; Collagen alpha-1(XI) chainEntrez Gene (Human): 1301Entrez Gene (Mouse) : 12814Entrez Gene (Rat) : 25654SwissProt (Human): P12107SwissProt (Mouse) : Q61245SwissProt (Rat) : P20909Storage/Stability : Shipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.
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Western blot analysis of Collagen 11 alpha 1 expression in CT26 (A) whole cell lysates.
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Immunohistochemical analysis of Collagen 11 alpha 1 staining in human breast cancer 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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Immunofluorescent analysis of Collagen 11 alpha 1 staining in K562 cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a humidified chamber. Cells were washed with PBST and incubated with a DyLight 594-conjugated secondary antibody (red) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).
COL11A1 promotes tumor progression and predicts poor clinical outcome in ovarian cancer
A response to Dr. Alzahrani's letter to the editor regarding the mechanism underlying fibrochondrogenesis
Expression of extracellular matrix components is disrupted in the immature and adult estrogen receptor ß-null mouse ovary