MNX1/HLXB9 Antibodies
We offer MNX1/HLXB9 Antibodies for use in common research applications: ELISA, Immunohistochemistry, Immunohistochemistry-Paraffin, Immunoprecipitation, Simple Western, Western Blot. Each MNX1/HLXB9 Antibody is fully covered by our Guarantee+, to give you complete peace of mind and the support when you need it. Our MNX1/HLXB9 Antibodies can be used in a variety of model species: Human, Mouse. Use the list below to choose the MNX1/HLXB9 Antibody which is most appropriate for your research; you can click on each one to view full technical details, images, references, reviews and related products. Choose from our MNX1/HLXB9 polyclonal antibodies.
Alternate Names for MNX1/HLXB9 Antibodies
anti-MNX1/HLXB9 antibody, anti-MNX1 antibody, anti-HB9 antibody, anti-HLXB9motor neuron and pancreas homeobox protein 1 antibody, anti-homeobox HB9 antibody, anti-HOXHB9Homeobox protein HB9 antibody, anti-motor neuron and pancreas homeobox 1 antibody, anti-SCRA1homeo box HB9 antibody
11 Results for "mnx1-hlxb9" in Primary Antibodies
![Immunocytochemistry/Immunofluorescence: MNX1/HLXB9 Antibody [NBP2-24691] - MCF7 cells were fixed in 4% paraformaldehyde for 10 minutes and permeabilized in 0.05% Triton X-100 in PBS for 5 minutes. The cells were incubated with anti-MNX1/HLXB9 NBP2-24691 at 1 ug/ml for 60 minutes at room temperature and detected with an anti-rabbit Dylight 488 (Green) at a 1:1000 dilution for 60 minutes. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 100X objective and digitally deconvolved.](http://images.novusbio.com/fullsize/MNX1-HLXB9-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-24691-img0003.jpg "Immunocytochemistry/Immunofluorescence: MNX1/HLXB9 Antibody [NBP2-24691] - MCF7 cells were fixed in 4% paraformaldehyde for 10 minutes and permeabilized in 0.05% Triton X-100 in PBS for 5 minutes. The cells were incubated with anti-MNX1/HLXB9 NBP2-24691 at 1 ug/ml for 60 minutes at room temperature and detected with an anti-rabbit Dylight 488 (Green) at a 1:1000 dilution for 60 minutes. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 100X objective and digitally deconvolved.")
![Immunocytochemistry/Immunofluorescence: MNX1/HLXB9 Antibody [NBP2-24691] - Neuro2a cells were fixed in 4% paraformaldehyde for 10 minutes and permeabilized in 0.05% Triton X-100 in PBS for 5 minutes. The cells were incubated with anti-MNX1/HLXB9 NBP2-24691 at 1 ug/ml for 60 minutes at room temperature and detected with an anti-rabbit Dylight 488 (Green) at a 1:1000 dilution for 60 minutes. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 100X objective and digitally deconvolved.](http://images.novusbio.com/fullsize/MNX1-HLXB9-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-24691-img0004.jpg)
![Western Blot: MNX1/HLXB9 Antibody [NBP2-24691] - Analysis of MNX1/HLXB9 in MOLT-4 cell lysates in the 1) absence and 2) presence of immunizing peptide using this antibody at 5 ug/ml. Goat anti-rabbit Ig HRP secondary antibody and PicoTect ECL substrate solution were used for this test.](http://images.novusbio.com/fullsize/MNX1-HLXB9-Antibody-Western-Blot-NBP2-24691-img0002.jpg)
![Immunohistochemistry-Paraffin: MNX1/HLXB9 Antibody [NBP2-24691] - Analysis of MNX1/HLXB9 in FFPE mouse pancreas tissue using an isotype control (top left) and this antibody (bottom left, right) at 5 ug/ml.](http://images.novusbio.com/fullsize/MNX1-HLXB9-Antibody-Immunohistochemistry-Paraffin-NBP2-24691-img0001.jpg)
![Western Blot: MNX1/HLXB9 Antibody [NBP3-13412] - Rat tissue extract (50 ug) was separated by 10% SDS-PAGE, and the membrane was blotted with MNX1/HLXB9 antibody (NBP3-13412) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/MNX1-HLXB9-Antibody-Western-Blot-NBP3-13412-img0003.jpg "Western Blot: MNX1/HLXB9 Antibody [NBP3-13412] - Rat tissue extract (50 ug) was separated by 10% SDS-PAGE, and the membrane was blotted with MNX1/HLXB9 antibody (NBP3-13412) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Immunohistochemistry-Frozen: MNX1/HLXB9 Antibody [NBP3-13412] - MNX1/HLXB9 antibody detects MNX1/HLXB9 protein by immunohistochemical analysis. Sample: Frozen-sectioned mouse spinal cord. Green: MNX1/HLXB9 stained by MNX1/HLXB9 antibody (NBP3-13412) diluted at 1:300. Blue: Hoechst 33342 staining.](http://images.novusbio.com/fullsize/MNX1-HLXB9-Antibody-Immunohistochemistry-Frozen-NBP3-13412-img0004.jpg)
![Western Blot: MNX1/HLXB9 Antibody [NBP3-13412] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with MNX1/HLXB9 antibody (NBP3-13412) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/MNX1-HLXB9-Antibody-Western-Blot-NBP3-13412-img0001.jpg)
![Western Blot: MNX1/HLXB9 Antibody [NBP3-13412] - Mouse tissue extract (50 ug) was separated by 10% SDS-PAGE, and the membrane was blotted with MNX1/HLXB9 antibody (NBP3-13412) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/MNX1-HLXB9-Antibody-Western-Blot-NBP3-13412-img0002.jpg)
![Western Blot: MNX1/HLXB9 Antibody [NBP3-16042] - Western blot analysis of extracts of Rat liver, using MNX1/HLXB9 antibody (NBP3-16042) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Enhanced Kit. Exposure time: 180s.](http://images.novusbio.com/fullsize/MNX1-HLXB9-Antibody-Western-Blot-NBP3-16042-img0001.jpg "Western Blot: MNX1/HLXB9 Antibody [NBP3-16042] - Western blot analysis of extracts of Rat liver, using MNX1/HLXB9 antibody (NBP3-16042) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Enhanced Kit. Exposure time: 180s.")
![Western Blot: MNX1/HLXB9 Antibody [NBP3-16042] - Western blot analysis of extracts of various cell lines, using MNX1/HLXB9 antibody (NBP3-16042) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 180s.](http://images.novusbio.com/fullsize/MNX1-HLXB9-Antibody-Western-Blot-NBP3-16042-img0002.jpg)
![Western Blot: MNX1/HLXB9 Antibody (JE32-08) [NBP3-32417] - Western blot analysis of MNX1/HLXB9 on different lysates with Rabbit anti-MNX1/HLXB9 antibody (NBP3-32417) at 1/1,000 dilution. Lane 1: HeLa cell lysate (15 ug/Lane) Lane 2: Raji cell lysate (15 ug/Lane) Lane 3: MCF7 cell lysate (15 ug/Lane) Lane 4: HepG2 cell lysate (15 ug/Lane) Lane 5: Huh7 cell lysate (15 ug/Lane) Lane 6: PANC-1 cell lysate (15 ug/Lane) Lane 7: SW1990 cell lysate (15 ug/Lane) Lane 8: Mouse pancreas tissue lysate (30 ug/Lane) Predicted band size: 41 kDa Observed band size: 41 kDa Exposure time: 5 seconds; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32417) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32417_rabbit-mnx1-hlxb9-mab-je32-08-278202415212475.jpg "Western Blot: MNX1/HLXB9 Antibody (JE32-08) [NBP3-32417] - Western blot analysis of MNX1/HLXB9 on different lysates with Rabbit anti-MNX1/HLXB9 antibody (NBP3-32417) at 1/1,000 dilution. Lane 1: HeLa cell lysate (15 ug/Lane) Lane 2: Raji cell lysate (15 ug/Lane) Lane 3: MCF7 cell lysate (15 ug/Lane) Lane 4: HepG2 cell lysate (15 ug/Lane) Lane 5: Huh7 cell lysate (15 ug/Lane) Lane 6: PANC-1 cell lysate (15 ug/Lane) Lane 7: SW1990 cell lysate (15 ug/Lane) Lane 8: Mouse pancreas tissue lysate (30 ug/Lane) Predicted band size: 41 kDa Observed band size: 41 kDa Exposure time: 5 seconds; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32417) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.")
![Western Blot: MNX1/HLXB9 Antibody (9P1B7) [NBP3-15861] - Western blot analysis of extracts of various cell lines, using MNX1/MNX1/HLXB9 Rabbit mAb (NBP3-15861) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 1s.](http://images.novusbio.com/fullsize/MNX1-HLXB9-Antibody-9P1B7-Western-Blot-NBP3-15861-img0001.jpg "Western Blot: MNX1/HLXB9 Antibody (9P1B7) [NBP3-15861] - Western blot analysis of extracts of various cell lines, using MNX1/MNX1/HLXB9 Rabbit mAb (NBP3-15861) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 1s.")
![Western Blot: MNX1/HLXB9 Antibody (SR1689) [NBP3-21816] - Western blot analysis using NBP3-21816 in Molt-4 cell lysate.](http://images.novusbio.com/fullsize/nbp3-21816_rabbit-mnx1-hlxb9-mab-sr1689-57202317161887.jpg "Western Blot: MNX1/HLXB9 Antibody (SR1689) [NBP3-21816] - Western blot analysis using NBP3-21816 in Molt-4 cell lysate.")
![Immunocytochemistry/Immunofluorescence: MNX1/HLXB9 Antibody [NBP2-57703] - Staining of human cell line MCF7 shows localization to nucleus. Antibody staining is shown in green.](http://images.novusbio.com/fullsize/MNX1-HLXB9-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-57703-img0001.jpg "Immunocytochemistry/Immunofluorescence: MNX1/HLXB9 Antibody [NBP2-57703] - Staining of human cell line MCF7 shows localization to nucleus. Antibody staining is shown in green.")
![Western Blot: MNX1/HLXB9 Antibody [NBP2-85301] - WB Suggested Anti-MNX1 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:62500. Positive Control: HepG2 cell lysate](http://images.novusbio.com/fullsize/MNX1-HLXB9-Antibody-Western-Blot-NBP2-85301-img0001.jpg "Western Blot: MNX1/HLXB9 Antibody [NBP2-85301] - WB Suggested Anti-MNX1 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:62500. Positive Control: HepG2 cell lysate")
![Western Blot: MNX1/HLXB9 Antibody [NBP2-99434] - Anti-MNX1/HLXB9 rabbit polyclonal antibody at 1:500 dilution. Lane A: Mouse spleen tissue lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 41 kDa. Observed band size: 41 kDa](http://images.novusbio.com/fullsize/MNX1-HLXB9-Antibody-Western-Blot-NBP2-99434-img0002.jpg "Western Blot: MNX1/HLXB9 Antibody [NBP2-99434] - Anti-MNX1/HLXB9 rabbit polyclonal antibody at 1:500 dilution. Lane A: Mouse spleen tissue lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 41 kDa. Observed band size: 41 kDa")