Mouse Mapk11 Antibody (N-term)

• Catalog Number: orb1788135
• Category: Antibodies
• Description: Affinity Purified Rabbit Polyclonal Antibody (Pab)
• Species/Host: Rabbit
• Clonality: Polyclonal
• Tested applications: FC, IHC-P, WB
• Predicted Reactivity: Human
• Reactivity: Mouse
• Isotype: Rabbit IgG
• Immunogen: 1-30 aa
• Antibody Type: Primary Antibody
• Dilution range: WB: 1:1000, IHC-P: 1:10~50, FC: 1:25
• Form/Appearance: Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
• Conjugation: Unconjugated
• MW: 41397 Da
• Target: This Mouse Mapk11 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of mouse Mapk11.
• UniProt ID: Q9WUI1
• NCBI: NP_035291.4
• Storage: Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles
• Alternative names: Mapk11; Prkm11; Mitogen-activated protein kinase 1
• Note: For research use only
• Expiration Date: 12 months from date of receipt.

Flow cytometric analysis of SH-SY5Y cells using Mouse Mapk11 Antibody (N-term) (green) compared to an isotype control of rabbit IgG (blue). Diluted at 1:25 dilution. An Alexa Fluor 488 goat anti-rabbit lgG at 1:400 dilution was used as the secondary antibody.

All lanes: Anti-Mapk11 Antibody (N-term) at 1/1000 dilution. Lane 1: mouse heart lysates. Lane 2: mouse spleen lysates. Lysates/proteins at 20 µg per lane. Secondary Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/10000 dilution. Predicted band size: 40 kDa. Blocking/Dilution buffer: 5% NFDM/TBST.

Mouse Mapk11 Antibody (N-term) immunohistochemistry analysis in formalin fixed and paraffin embedded mouse live tissue followed by peroxidase conjugation of the secondary antibody and DAB staining. This data demonstrates the use of Mouse Mapk11 Antibody (N-term) for immunohistochemistry. Clinical relevance has not been evaluated.