Antibody data
- Antibody Data
- Antigen structure
- References [0]
- Comments [0]
- Validations
- Immunocytochemistry [5]
- Flow cytometry [1]
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- Product number
- MA5-41253 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- CRM1 Recombinant Rabbit Monoclonal Antibody (JB35-22)
- Antibody type
- Monoclonal
- Antigen
- Recombinant full-length protein
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Isotype
- IgG
- Antibody clone number
- JB35-22
- Vial size
- 100 µL
- Concentration
- 1 mg/mL
- Storage
- Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
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- Experimental details
- Immunocytochemistry/Immunofluorescence analysis of CRM1 in LOVO cells (green) using CRM1 Recombinant Monoclonal Antibody (Product # MA5-41253). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. The nuclear counter stain is DAPI (blue).
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunocytochemistry/Immunofluorescence analysis of CRM1 in SiHa cells (green) using CRM1 Recombinant Monoclonal Antibody (Product # MA5-41253). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. The nuclear counter stain is DAPI (blue).
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunocytochemistry/Immunofluorescence analysis of CRM1 in A431 cells (green) using CRM1 Recombinant Monoclonal Antibody (Product # MA5-41253). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. The nuclear counter stain is DAPI (blue).
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunofluorescence analysis of XPO1 was performed using 70% confluent log phase HeLa cells. The cells were fixed with 4% paraformaldehyde for 15 minutes, permeabilized with 0.1% Triton™ X-100 for 15 minutes, and blocked with 2% BSA for 45 minutes at room temperature. The cells were labeled with CRM1 Recombinant Rabbit Monoclonal Antibody (JB35-22) (Product # MA5-41253) at 1:100 dilution in 0.1% BSA, incubated at 4 degree celsius overnight and then labeled with Donkey anti-Rabbit IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor Plus 488 (Product # A32790), (1:2000 dilution), for 45 minutes at room temperature (Panel a: Green). Nuclei (Panel b:Blue) were stained with ProLong™ Diamond Antifade Mountant with DAPI (Product # P36962). F-actin (Panel c: Red) was stained with Rhodamine Phalloidin (Product # R415, 1:300 dilution). Panel d represents the merged image showing nuclear localization. Panel e represents control cells with no primary antibody to assess background. The images were captured at 40X magnification in CellInsight CX7 LZR High-Content Screening (HCS) Platform (Product # CX7A1110LZR) and externally deconvoluted (D.Sage et al. / Methods 115 (2017) 28–41).
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Knockdown of XPO1 was achieved by transfecting HeLa cells with XPO1 specific siRNA (Silencer® select Product # s14937, S1439). Immunofluorescence analysis was performed on untransfected HeLa cells (panel a,d), transfected with non-specific scrambled siRNA (panels b,e) and transfected with XPO1 specific siRNA (panel c,f). Cells were fixed, permeabilized, and labelled with CRM1 Recombinant Rabbit Monoclonal Antibody (JB35-22) (Product # MA5-41253, 1:100 dilution) followed by Goat anti-Rabbit IgG (H+L) Superclonal™ Recombinant Secondary Antibody, Alexa Fluor® 488 conjugate (Product # A27034), (1:2000 dilution). Nuclei (blue) were stained using ProLong™ Diamond Antifade Mountant with DAPI (Product # P36962), and Rhodamine Phalloidin (Product # R415, 1:300 dilution) was used for cytoskeletal F-actin (Red) staining. Knockdown of specific signal was observed upon siRNA mediated knockdown (panel c,f) confirming specificity of the antibody to XPO1 (Green). The Images were captured at 60X magnification.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Flow Cytometry analysis of CRM1 in K562 cells. The cells were fixed, permeabilized and stained with CRM1 Recombinant Monoclonal Antibody (Product # MA5-41253) at a dilution of 1:100 (red). Alexa Fluor 488-conjugated goat anti rabbit IgG was used as the secondary antibody. Unlabelled control (cells without incubation with primary antibody; black).