Note: Mouseover a species abbreviation on the product page to display the fullname.
How can we help you?
![Western Blot: WDR5 Antibody (2C2) [H00011091-M01] - WDR5 monoclonal antibody (M01), clone 2C2. Analysis of WDR5 expression in A-549.](http://images.novusbio.com/fullsize/WDR5-Antibody-2C2-Western-Blot-H00011091-M01-img0008.jpg "Western Blot: WDR5 Antibody (2C2) [H00011091-M01] - WDR5 monoclonal antibody (M01), clone 2C2. Analysis of WDR5 expression in A-549.")
![Immunocytochemistry/Immunofluorescence: WDR5 Antibody (2C2) [H00011091-M01] - Analysis of monoclonal antibody to WDR5 on HeLa cell. Antibody concentration 10 ug/ml.](http://images.novusbio.com/fullsize/WDR5-Antibody-2C2-Immunocytochemistry-Immunofluorescence-H00011091-M01-img0006.jpg)
![Western Blot: WDR5 Antibody (2C2) [H00011091-M01] - WDR5 monoclonal antibody (M01), clone 2C2. Analysis of WDR5 expression in Hs 181.Tes.](http://images.novusbio.com/fullsize/WDR5-Antibody-2C2-Western-Blot-H00011091-M01-img0009.jpg)
![Sandwich ELISA: WDR5 Antibody (2C2) [H00011091-M01] - Detection limit for recombinant GST tagged WDR5 is approximately 0.3ng/ml as a capture antibody.](http://images.novusbio.com/fullsize/WDR5-Antibody-2C2-Sandwich-ELISA-H00011091-M01-img0007.jpg)
![Western Blot: WDR5 Antibody [NBP3-18669] - Figure 3. Western blot analysis using the antibody directed against WDR5 Nclear extracts from HeLa cells (20 ug) were analysed by Western blot using the antibody against WDR5 diluted 1:1,000 in TBS-Tween containing 5% skimmed milk. The position of the protein of interest is indicated on the right; the marker (in kDa) is shown on the left.](http://images.novusbio.com/fullsize/WDR5-Antibody-Western-Blot-NBP3-18669-img0001.jpg "Western Blot: WDR5 Antibody [NBP3-18669] - Figure 3. Western blot analysis using the antibody directed against WDR5 Nclear extracts from HeLa cells (20 ug) were analysed by Western blot using the antibody against WDR5 diluted 1:1,000 in TBS-Tween containing 5% skimmed milk. The position of the protein of interest is indicated on the right; the marker (in kDa) is shown on the left.")
![Immunocytochemistry/Immunofluorescence: WDR5 Antibody [NBP3-18669] - Figure 4. Immunofluorescence using the antibody directed against WDR HeLa cells were stained with the antibody against WDR5 and with DAPI. Cells were fixed with 4% formaldehyde for 10 and blocked with PBS/TX-100 containing 5% normal goat serum and 1% BSA. The cells were immunofluorescently labeled with the WDR5 antibody (left) diluted 1:1,000 in blocking solution followed by an anti-rabbit antibody conjugated to Alexa488. The middle panel shows staining of the nuclei with DAPI. A merge of the two stainings is shown on the right.](http://images.novusbio.com/fullsize/WDR5 Antibody-Immunocytochemistry-Immunofluorescence-NBP3-18669-img0003.jpg)
![Chromatin Immunoprecipitation (ChIP): WDR5 Antibody [NBP3-18669] - Figure 1. ChIP results obtained with antibody directed against WDR5. ChIP assays performed using HeLa cells, antibody against WDR5 and optimized PCR primer sets for qPCR. ChIP performed with the](http://images.novusbio.com/fullsize/WDR5-Antibody-Chromatin-Immunoprecipitation-ChIP-NBP3-18669-img0004.jpg)
![Chromatin Immunoprecipitation Sequencing: WDR5 Antibody [NBP3-18669] - Figure 2. ChIP-seq results obtained with the antibody directed against WDR5 ChIP was performed on sheared chromatin from 4 million HeLa cells using 2 ug of the antibody against WDR5 as described above. The IPd DNA was subsequently analysed on an Illumina HiSeq. Library preparation, cluster generation and sequencing were performed according to the manufacturers instructions. The 50 bp tags were aligned to the human genome using the BWA algorithm. Figure 2 shows the enrichment along the complete sequence and a 2 Mb region of human chromosome 1 (fig 2A and B), and in two genomic regions surrounding the RPL41 and RPS4X positive control genes (fig 2C and D).](http://images.novusbio.com/fullsize/WDR5-Antibody-Chromatin-Immunoprecipitation-Sequencing-NBP3-18669-img0002.jpg)
![Western Blot: WDR5 Antibody [NBP1-30070] - Detection of mouse and rat WDR5 by western blot. Samples: Whole cell lysate (50 ug) from NIH 3T3, TCMK-1, 4T1, CT26.WT, and rat C6 cells. Antibodies: Affinity purified rabbit anti-WDR5 antibody NBP1-30070 used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.](http://images.novusbio.com/fullsize/WDR5-Antibody-Western-Blot-NBP1-30070-img0003.jpg "Western Blot: WDR5 Antibody [NBP1-30070] - Detection of mouse and rat WDR5 by western blot. Samples: Whole cell lysate (50 ug) from NIH 3T3, TCMK-1, 4T1, CT26.WT, and rat C6 cells. Antibodies: Affinity purified rabbit anti-WDR5 antibody NBP1-30070 used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.")
![Immunohistochemistry-Paraffin: WDR5 Antibody [NBP1-30070] - Sample: FFPE section of human breast carcinoma. Antibody: Affinity purified rabbit anti- WDR5 used at a dilution of 1:200 (1ug/ml). Detection: DAB](http://images.novusbio.com/fullsize/WDR5-Antibody-Immunohistochemistry-NBP1-30070-img0002.jpg)
![Western Blot: WDR5 Antibody [NBP1-30070] - Whole cell lysate from HeLa, 293T, and mouse NIH3T3 cells. WDR5 was successfully IPed by NBP1-30063.](http://images.novusbio.com/fullsize/WDR5-Antibody-Western-Blot-NBP1-30070-img0001.jpg)
![Flow Cytometry: WDR5 Antibody (RAB-C223) - Chimeric - Azide and BSA Free [NBP3-20133] - Paraformaldehyde fixed HeLa cells permeabilized with 0.5% Triton were stained with anti-unknown specificity antibody (isotype control, black line) or the rabbit IgG version of RAB-C223 (NBP3-20133, 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/nbp3-20133_rabbit-wdr5-mab-rab-c223-chimeric-azide-and-bsa-free-2742023924296.png "Flow Cytometry: WDR5 Antibody (RAB-C223) - Chimeric - Azide and BSA Free [NBP3-20133] - Paraformaldehyde fixed HeLa cells permeabilized with 0.5% Triton were stained with anti-unknown specificity antibody (isotype control, black line) or the rabbit IgG version of RAB-C223 (NBP3-20133, 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.")
![Western Blot: WDR5 Antibody (RAB-C223) - Chimeric - Azide and BSA Free [NBP3-20133] - Nuclear lysate of MCF7 cells (35ug protein in RIPA buffer) were resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of RAB-C223 (NBP3-20133) at 1 ug/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.](http://images.novusbio.com/fullsize/nbp3-20133_rabbit-wdr5-mab-rab-c223-chimeric-azide-and-bsa-free-2742023924242.png)
![Immunocytochemistry/Immunofluorescence: WDR5 Antibody (RAB-C223) - Chimeric - Azide and BSA Free [NBP3-20133] - Immunofluorescence analysis of paraformaldehyde fixed HeLa cells permeabilized with 0.15% Triton stained with the chimeric rabbit IgG version of RAB-C223 (NBP3-20133) (1:100 dilution) for 1h followed by Alexa Fluor(R) 488 secondary antibody (1:1500 dilution), showing nuclear and cytoplasmic staining. Actin filaments were stained with phalloidin (red) and the nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-20133, 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/nbp3-20133_rabbit-wdr5-mab-rab-c223-chimeric-azide-and-bsa-free-2742023964611.png)
![Immunohistochemistry-Paraffin: WDR5 Antibody [NBP1-30063] - Sample: FFPE section of human ovarian carcinoma. Antibody: Affinity purified rabbit anti-fs18 WDR5 fs20 used at a dilution of 1:1,000 (1ug/ml). Detection: DAB](http://images.novusbio.com/fullsize/WDR5-Antibody-Immunohistochemistry-NBP1-30063-img0004.jpg "Immunohistochemistry-Paraffin: WDR5 Antibody [NBP1-30063] - Sample: FFPE section of human ovarian carcinoma. Antibody: Affinity purified rabbit anti-fs18 WDR5 fs20 used at a dilution of 1:1,000 (1ug/ml). Detection: DAB")
![<b>Independent Antibodies Validation. </b>Immunoprecipitation: WDR5 Antibody [NBP1-30063] - Detection of human WDR5 by western blot of immunoprecipitates. Samples: Whole cell lysate (0.5 or 1.0 mg per IP reaction; 20% of IP loaded) from HeLa cells. Antibodies: Affinity purified rabbit anti-WDR5 antibody A302-429A (lot A302-429A-2) used for IP at 6 ug per reaction. WDR5 was also immunoprecipitated by rabbit anti-WDR5 antibody A302-430A. For blotting immunoprecipitated WDR5, A302-430A was used at 1 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.](http://images.novusbio.com/fullsize/WDR5-Antibody-Immunoprecipitation-NBP1-30063-img0006.jpg)
![Western Blot: WDR5 Antibody [NBP3-18672] - Figure 2. Western blot analysis using the antibody directed against Wdr5 (1) Western blot was performed on whole cell lysates from mouse fibroblasts (NIH3T3) and embryonic stem cells (E14Tg2a) with the antibody against mouse Wdr5 , diluted 1:1,000 in BSA/PBS- Tween. The molecular weight marker (M, in kDa) is shown on the left; the location of the protein of interest (36 kDa) is indicated on the right.](http://images.novusbio.com/fullsize/WDR5-Antibody-Western-Blot-NBP3-18672-img0001.jpg "Western Blot: WDR5 Antibody [NBP3-18672] - Figure 2. Western blot analysis using the antibody directed against Wdr5 (1) Western blot was performed on whole cell lysates from mouse fibroblasts (NIH3T3) and embryonic stem cells (E14Tg2a) with the antibody against mouse Wdr5 , diluted 1:1,000 in BSA/PBS- Tween. The molecular weight marker (M, in kDa) is shown on the left; the location of the protein of interest (36 kDa) is indicated on the right.")
![ELISA: WDR5 Antibody [NBP3-18672] - Figure 1. Determination of the titer To determine the titer, an ELISA was performed using a serial dilution of the antibody directed against mouse Wdr5 . By plotting the absorbance against the antibody dilution (Figure 1), the titer of the antibody was estimated to be 1:12,300.](http://images.novusbio.com/fullsize/WDR5 Antibody-ELISA-NBP3-18672-img0002.jpg)
![Immunohistochemistry: WDR5 Antibody (18D11) [NBP3-26253] - Image of WDR5 Antibody (18D11) diluted at 1:50 and staining in paraffin-embedded human testis tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.79% DAB.](http://images.novusbio.com/fullsize/nbp3-26253_rabbit-wdr5-mab-18d11-262202415355722.jpg "Immunohistochemistry: WDR5 Antibody (18D11) [NBP3-26253] - Image of WDR5 Antibody (18D11) diluted at 1:50 and staining in paraffin-embedded human testis tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.79% DAB.")
![Flow Cytometry: WDR5 Antibody (18D11) [NBP3-26253] - Overlay Peak curve showing Hela cells stained with WDR5 Antibody (18D11) (red line) at 1:50. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26253_rabbit-wdr5-mab-18d11-282202414312739.jpg)
![Western Blot: WDR5 Antibody (S05-4D3) [NBP3-14984] - Western blot detection of WDR5 in K562, C6, 3T3, Hela cell lysates using WDR5 Rabbit mAb (1:1000 diluted). Predicted band size: 37kDa. Observed band size: 37kDa.](http://images.novusbio.com/fullsize/WDR5-Antibody-S05-4D3-Western-Blot-NBP3-14984-img0001.jpg "Western Blot: WDR5 Antibody (S05-4D3) [NBP3-14984] - Western blot detection of WDR5 in K562, C6, 3T3, Hela cell lysates using WDR5 Rabbit mAb (1:1000 diluted). Predicted band size: 37kDa. Observed band size: 37kDa.")
![Western Blot: WDR5 Antibody (3S6R9) [NBP3-16162] - Western blot analysis of extracts of various cell lines, using WDR5 Rabbit mAb (NBP3-16162) 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: 10s.](http://images.novusbio.com/fullsize/WDR5-Antibody-3S6R9-Western-Blot-NBP3-16162-img0001.jpg "Western Blot: WDR5 Antibody (3S6R9) [NBP3-16162] - Western blot analysis of extracts of various cell lines, using WDR5 Rabbit mAb (NBP3-16162) 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: 10s.")
![Immunocytochemistry/Immunofluorescence: WDR5 Antibody [NBP2-55518] - Staining of human cell line U-2 OS shows localization to nucleoplasm.](http://images.novusbio.com/fullsize/WDR5-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-55518-img0001.jpg "Immunocytochemistry/Immunofluorescence: WDR5 Antibody [NBP2-55518] - Staining of human cell line U-2 OS shows localization to nucleoplasm.")