UBE2I/Ubc9 Antibodies
We offer UBE2I/Ubc9 Antibodies for use in common research applications: ELISA, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Immunohistochemistry-Paraffin, Peptide ELISA, Western Blot. Each UBE2I/Ubc9 Antibody is fully covered by our Guarantee+, to give you complete peace of mind and the support when you need it. Our UBE2I/Ubc9 Antibodies can be used in a variety of model species: Human, Mouse, Primate, Rat. Use the list below to choose the UBE2I/Ubc9 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 UBE2I/Ubc9 polyclonal antibodies and browse our UBE2I/Ubc9 monoclonal antibody catalog.
Alternate Names for UBE2I/Ubc9 Antibodies
anti-UBE2I/Ubc9 antibody, anti-UBE2I antibody, anti-C358B7.1 antibody, anti-EC 6.3.2 antibody, anti-EC 6.3.2.- antibody, anti-p18 antibody, anti-SUMO-1-protein ligase antibody, anti-SUMO-protein ligase antibody, anti-UBC9SUMO-conjugating enzyme UBC9 antibody, anti-UBCE9 antibody, anti-Ubiquitin carrier protein 9 antibody, anti-Ubiquitin carrier protein I antibody, anti-ubiquitin conjugating enzyme 9 antibody, anti-Ubiquitin-conjugating enzyme E2 I antibody, anti-ubiquitin-conjugating enzyme E2I (homologous to yeast UBC9) antibody, anti-ubiquitin-conjugating enzyme E2I (UBC9 homolog, yeast) antibody, anti-ubiquitin-conjugating enzyme UbcE2A antibody, anti-ubiquitin-like protein SUMO-1 conjugating enzyme antibody, anti-ubiquitin-protein ligase E2I antibody, anti-Ubiquitin-protein ligase I antibody
13 Results for "ube2i-ubc9" in Primary Antibodies
![Western Blot: UBE2I/Ubc9 Antibody [NBP1-86887] - Lane 1: NIH-3T3 cell lysate (Mouse embryonic fibroblast cells); Lane 2: NBT-II cell lysate (Rat Wistar bladder tumour cells).](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-Western-Blot-NBP1-86887-img0003.jpg "Western Blot: UBE2I/Ubc9 Antibody [NBP1-86887] - Lane 1: NIH-3T3 cell lysate (Mouse embryonic fibroblast cells); Lane 2: NBT-II cell lysate (Rat Wistar bladder tumour cells).")
![Immunocytochemistry/Immunofluorescence: UBE2I/Ubc9 Antibody [NBP1-86887] - Staining of human cell line U-2 OS shows localization to cytosol. Antibody staining is shown in green.](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-86887-img0006.jpg)
![Immunohistochemistry-Paraffin: UBE2I/Ubc9 Antibody [NBP1-86887] - Staining of human testis shows moderate to strong nuclear positivity in cells in seminiferous ducts.](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-Immunohistochemistry-Paraffin-NBP1-86887-img0010.jpg)
![Western Blot: UBE2I/Ubc9 Antibody [NBP1-86887] - Lane 1: Marker [kDa] 230, 130, 95, 72, 56, 36, 28, 17, 11Lane 2: Human cell line RT-4Lane 3: Human cell line U-251MG sp](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-Western-Blot-NBP1-86887-img0004.jpg)
![Immunohistochemistry-Paraffin: UBE2I/Ubc9 Antibody [NBP1-86887] - Staining of human placenta shows moderate to strong nuclear positivity in trophoblastic cells.](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-Immunohistochemistry-Paraffin-NBP1-86887-img0007.jpg)
![Immunohistochemistry-Paraffin: UBE2I/Ubc9 Antibody [NBP1-86887] - Staining of human tonsil shows moderate to strong nuclear positivity in non - germinal center cells.](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-Immunohistochemistry-Paraffin-NBP1-86887-img0008.jpg)
![Immunohistochemistry-Paraffin: UBE2I/Ubc9 Antibody [NBP1-86887] - Staining of human fallopian tube shows moderate to strong nuclear positivity in glandular cells.](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-Immunohistochemistry-Paraffin-NBP1-86887-img0009.jpg)
![Western Blot: UBE2I/Ubc9 Antibody [NB300-812] - Staining of Rat Ovary lysate (35 ug protein in RIPA buffer). Detected by chemiluminescence.](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-Western-Blot-NB300-812-img0007.jpg "Western Blot: UBE2I/Ubc9 Antibody [NB300-812] - Staining of Rat Ovary lysate (35 ug protein in RIPA buffer). Detected by chemiluminescence.")
![Immunohistochemistry-Paraffin: UBE2I/Ubc9 Antibody [NB300-812] - Human breast cancer tissue. IHC-P image submitted by a verified customer review.](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-Immunohistochemistry-Paraffin-NB300-812-img0008.jpg)
![Western Blot: UBE2I/Ubc9 Antibody [NB300-812] - Staining of Human Kidney lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-Western-Blot-NB300-812-img0004.jpg)
![Immunohistochemistry-Paraffin: UBE2I/Ubc9 Antibody [NB300-812] - Staining of Human Kidney. Antibody at 0.3 ug/mL. Microwaved antigen retrieval with Tris/EDTA buffer pH9, HRP-staining.](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-Immunohistochemistry-Paraffin-NB300-812-img0006.jpg)
![Western Blot: UBE2I/Ubc9 Antibody (6Z9V6) [NBP3-16400] - Western blot analysis of extracts of various cell lines, using UBE2I/Ubc9 Rabbit mAb (NBP3-16400) 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/UBE2I-Ubc9-Antibody-6Z9V6-Western-Blot-NBP3-16400-img0004.jpg "Western Blot: UBE2I/Ubc9 Antibody (6Z9V6) [NBP3-16400] - Western blot analysis of extracts of various cell lines, using UBE2I/Ubc9 Rabbit mAb (NBP3-16400) 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.")
![Immunohistochemistry-Paraffin: UBE2I/Ubc9 Antibody (6Z9V6) [NBP3-16400] - Immunohistochemistry of paraffin-embedded mouse spinal cord using UBE2I/Ubc9 Rabbit mAb (NBP3-16400) at dilution of 1:100 (40x lens).Perform microwave antigen retrieval with 10 mM PBS buffer pH 7.2 before commencing with IHC staining protocol.](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-6Z9V6-Immunohistochemistry-Paraffin-NBP3-16400-img0003.jpg)
![Western Blot: UBE2I/Ubc9 Antibody (6Z9V6) [NBP3-16400] - Western blot analysis of extracts of HeLa cells, using UBE2I/Ubc9 Rabbit mAb (NBP3-16400) 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: 30s.](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-6Z9V6-Western-Blot-NBP3-16400-img0005.jpg)
![Immunohistochemistry-Paraffin: UBE2I/Ubc9 Antibody (6Z9V6) [NBP3-16400] - Immunohistochemistry of paraffin-embedded rat brain using UBE2I/Ubc9 Rabbit mAb (NBP3-16400) at dilution of 1:100 (40x lens).Perform microwave antigen retrieval with 10 mM PBS buffer pH 7.2 before commencing with IHC staining protocol.](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-6Z9V6-Immunohistochemistry-Paraffin-NBP3-16400-img0001.jpg)
![Immunohistochemistry-Paraffin: UBE2I/Ubc9 Antibody (6Z9V6) [NBP3-16400] - Immunohistochemistry of paraffin-embedded human colon carcinoma using UBE2I/Ubc9 Rabbit mAb (NBP3-16400) at dilution of 1:100 (40x lens).Perform microwave antigen retrieval with 10 mM PBS buffer pH 7.2 before commencing with IHC staining protocol.](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-6Z9V6-Immunohistochemistry-Paraffin-NBP3-16400-img0002.jpg)
![Western Blot: UBE2I/Ubc9 Antibody [NBP2-93799] - Western blot analysis of extracts of various cell lines, using (NBP2-93799) 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: 30s.](http://images.novusbio.com/fullsize/UBE2I-Ubc9 Antibody-Western Blot-NBP2-93799-img0002.jpg "Western Blot: UBE2I/Ubc9 Antibody [NBP2-93799] - Western blot analysis of extracts of various cell lines, using (NBP2-93799) 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: 30s.")
![Immunohistochemistry-Paraffin: UBE2I/Ubc9 Antibody [NBP2-93799] - Immunohistochemistry of paraffin-embedded rat lung using UBE2I/Ubc9 Rabbit pAb (NBP2-93799) at dilution of 1:100 (40x lens). Perform high pressure antigen retrieval with 10 mM citrate buffer pH 6.0 before commencing with IHC staining protocol.](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-Immunohistochemistry-Paraffin-NBP2-93799-img0001.jpg)
![Western Blot: UBE2I/Ubc9 Antibody [NBP3-00096] - Anti-UBE2I/Ubc9 rabbit polyclonal antibody at 1:500 dilution. Lane A: Jurkat Whole Cell Lysate Lane B: A431 Whole Cell Lysate Lane C: NIH-3T3 Whole Cell Lysate Lane D: PC12 Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H&L) /Dylight 800 at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 18 kDa. Observed band size: 18 kDa](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-Western-Blot-NBP3-00096-img0003.jpg "Western Blot: UBE2I/Ubc9 Antibody [NBP3-00096] - Anti-UBE2I/Ubc9 rabbit polyclonal antibody at 1:500 dilution. Lane A: Jurkat Whole Cell Lysate Lane B: A431 Whole Cell Lysate Lane C: NIH-3T3 Whole Cell Lysate Lane D: PC12 Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H&L) /Dylight 800 at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 18 kDa. Observed band size: 18 kDa")
![Immunocytochemistry/Immunofluorescence: UBE2I/Ubc9 Antibody [NBP3-00096] - Immunofluorescence staining of UBE2I/Ubc9 in HeLa cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS, blocked with 10% serum, and incubated with rabbit anti-human UBE2I/Ubc9 polyclonal antibody (dilution ratio 1:1000) at 4C overnight. Then cells were stained with the Alexa Fluor(R)488-conjugated Goat Anti-rabbit IgG secondary antibody (green).Positive staining was localized to cytoplasm and nucleus.](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-00096-img0002.jpg)
![Immunoprecipitation: UBE2I/Ubc9 Antibody [NBP3-00096] - UBE2I/Ubc9 was immunoprecipitated using: Lane A: 0.5 mg Jurkat Whole Cell Lysate Lane B: 0.5 mg Hela Whole Cell Lysate Lane C: 0.5 mg A431 Whole Cell Lysate 2 ul anti-UBE2I/Ubc9 rabbit polyclonal antibody and 15 ul of 50 % Protein G agarose. Primary antibody: Anti-UBE2I/Ubc9 rabbit polyclonal antibody, at 1:100 dilution. Secondary antibody: Dylight 800-labeled antibody to rabbit IgG (H+L), at 1:5000 dilution Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 18 kDa. Observed band size: 18 kDa](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-Immunoprecipitation-NBP3-00096-img0001.jpg)
![Flow Cytometry: UBE2I/Ubc9 Antibody (SAIC-36A-9) - Azide and BSA Free [NBP3-20104] - Paraformaldehyde fixed Jurkat cells permeabilized with 0.5% Triton were stained with anti-unknown specificity antibody (isotype control, black line) or the rabbit IgG version of SAIC-36A-9 (NBP3-20104, blue line) at a dilution of 1:100 for 1h at RT. After washing, the bound antibody was detected using a goat anti-rabbit IgG AlexaFluor(R) 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/nbp3-20104_rabbit-ube2i-ubc9-mab-saic-36a-9-azide-and-bsa-free-2742023924280.png "Flow Cytometry: UBE2I/Ubc9 Antibody (SAIC-36A-9) - Azide and BSA Free [NBP3-20104] - Paraformaldehyde fixed Jurkat cells permeabilized with 0.5% Triton were stained with anti-unknown specificity antibody (isotype control, black line) or the rabbit IgG version of SAIC-36A-9 (NBP3-20104, blue line) at a dilution of 1:100 for 1h at RT. After washing, the bound antibody was detected using a goat anti-rabbit IgG AlexaFluor(R) 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.")
![Immunocytochemistry/Immunofluorescence: UBE2I/Ubc9 Antibody (SAIC-36A-9) - Azide and BSA Free [NBP3-20104] - Immunofluorescence analysis of paraformaldehyde fixed Jurak cells on Shi-fix(TM) cover-slips stained with the chimeric rabbit IgG version of SAIC-36A-9 (NBP3-20104) (1:100 dilution) for 1h followed by Alexa Fluor(R) 488 secondary antibody (1:1000 dilution), showing nuclear staining. Actin filaments were stained with phalloidin (red) and the nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-20104, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor(R) 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp3-20104_rabbit-ube2i-ubc9-mab-saic-36a-9-azide-and-bsa-free-2742023924286.png)
![Western Blot: UBE2I/Ubc9 Antibody [NBP2-95142] - Western blot analysis of extracts of SW620 cells, using UBE2I/Ubc9 Rabbit pAb (NBP2-95142) 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.](http://images.novusbio.com/fullsize/UBE2I-Ubc9 Antibody-Western Blot-NBP2-95142-img0002.jpg "Western Blot: UBE2I/Ubc9 Antibody [NBP2-95142] - Western blot analysis of extracts of SW620 cells, using UBE2I/Ubc9 Rabbit pAb (NBP2-95142) 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.")
![Immunocytochemistry/Immunofluorescence: UBE2I/Ubc9 Antibody [NBP2-95142] - Analysis of U2OS cells using UBE2I/Ubc9 . Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/UBE2I-Ubc9-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-95142-img0001.jpg)
![UBE2I/Ubc9 Antibody (SAIC-36A-9) [mFluor Violet 450 SE] [NBP3-20104MFV450] - Vial of mFluor Violet 450 conjugated antibody. mFluor Violet 450 is optimally excited at 406 nm by the Violet laser (405 nm) and has an emission maximum of 445 nm.](http://images.novusbio.com/fullsize/nbp3-20104mfv450_rabbit-ube2i-ubc9-mab-saic-36a-9-mfluor-violet-450-se-226202313291044.png "UBE2I/Ubc9 Antibody (SAIC-36A-9) [mFluor Violet 450 SE] [NBP3-20104MFV450] - Vial of mFluor Violet 450 conjugated antibody. mFluor Violet 450 is optimally excited at 406 nm by the Violet laser (405 nm) and has an emission maximum of 445 nm.")