| Conjugate | Catalog # | Availability | Size | Price |
|---|---|---|---|---|
| Alexa Fluor Plus 488 | NBP2-44234AFP488 | |||
| Alexa Fluor Plus 555 | NBP2-44234AFP555 | |||
| Alexa Fluor Plus 594 | NBP2-44234AFP594 | |||
| Alexa Fluor Plus 647 | NBP2-44234AFP647 | |||
| Alexa Fluor Plus 680 | NBP2-44234AFP680 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-81894-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-20769 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-70172 | |||
![Western Blot: Hexokinase 2 Antibody [NBP2-44234] - Western Blot of Rabbit Hexokinase 2 2 antibody. Lane 1: Molecular Weight Marker. Lane 2: Hexokinase 2. Primary Antibody: Anti-Hexokinase 2 at 1:1000 overnight in 2-8C. Secondary Antibody: Goat Anti-Rabbit IgG HRP at 1:40,000 for 30 mins at RT. Block: Blocking buffer for 30 mins at RT. Expect MW: ~54kDa.](http://images.novusbio.com/fullsize/Hexokinase-2-Antibody-Western-Blot-NBP2-44234-img0002.jpg "Western Blot: Hexokinase 2 Antibody [NBP2-44234] - Western Blot of Rabbit Hexokinase 2 2 antibody. Lane 1: Molecular Weight Marker. Lane 2: Hexokinase 2. Primary Antibody: Anti-Hexokinase 2 at 1:1000 overnight in 2-8C. Secondary Antibody: Goat Anti-Rabbit IgG HRP at 1:40,000 for 30 mins at RT. Block: Blocking buffer for 30 mins at RT. Expect MW: ~54kDa.")
![ELISA: Hexokinase 2 Antibody [NBP2-44234] - ELISA Results of Rabbit Hexokinase 2 2 antibody tested against purified Hexokinase 2. Each well was coated in duplicate with 1.0 ug of Hexokinase 2 (Yeast). The starting dilution of antibody was 5ug/ml and the X-axis represents the Log10 of a 3-fold dilution. This titration is a 4-parameter curve fit where the IC50 is defined as the titer of the antibody. Assay performed using HRP Conjugate Stabilizer, Goat Anti-Rabbit IgG HRP conjugated and TMB substrate.](http://images.novusbio.com/fullsize/Hexokinase-2-Antibody-ELISA-NBP2-44234-img0001.jpg)
![Western Blot: MACF1 Antibody [NBP2-36528] - Samples: Whole cell lysate (50 ug) from HeLa, 293T, Jurkat, mouse TCMK-1, and mouse NIH3T3 cells prepared using NETN lysis buffer. Antibodies: Affinity purified rabbit anti-MACF1 antibody used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.](http://images.novusbio.com/fullsize/MACF1-Antibody-Western-Blot-NBP2-36528-img0001.jpg "<b>Biological Strategies Validation. </b>Western Blot: MACF1 Antibody [NBP2-36528] - Samples: Whole cell lysate (50 ug) from HeLa, 293T, Jurkat, mouse TCMK-1, and mouse NIH3T3 cells prepared using NETN lysis buffer. Antibodies: Affinity purified rabbit anti-MACF1 antibody used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.")
![Immunohistochemistry: SPECC1L Antibody - BSA Free [NBP3-48053] - Immunohistochemistry of paraffin-embedded human testis tissue slide using (SPECC1L Antibody) at dilution of 1:50](http://images.novusbio.com/fullsize/nbp3-48053_rabbit-specc1l-pab-bsa-free-28420251156180.jpg "Immunohistochemistry: SPECC1L Antibody - BSA Free [NBP3-48053] - Immunohistochemistry of paraffin-embedded human testis tissue slide using (SPECC1L Antibody) at dilution of 1:50")
![Western Blot: SPECC1L Antibody - BSA Free [NBP3-48053] - NIH/3T3 cells were subjected to SDS PAGE followed by western blot with (SPECC1L Antibody) at dilution of 1:600](http://images.novusbio.com/fullsize/nbp3-48053_rabbit-specc1l-pab-bsa-free-284202511492254.jpg)
![Western Blot: EGFR [p Tyr1092] Antibody [NB100-81894] - Analysis of extracts from A431 cells untreated or treated with EGF using EGFR(Phospho-Tyr1092) antibody.](http://images.novusbio.com/fullsize/EGFR-[p-Tyr1092]-Antibody-Western-Blot-NB100-81894-img0005.jpg "<b>Biological Strategies Validation. </b>Western Blot: EGFR [p Tyr1092] Antibody [NB100-81894] - Analysis of extracts from A431 cells untreated or treated with EGF using EGFR(Phospho-Tyr1092) antibody.")
![<b>Biological Strategies Validation. </b>Immunohistochemistry-Paraffin: EGFR [p Tyr1092] Antibody [NB100-81894] - Analysis of paraffin- embedded human breast carcinoma tissue using NB100-81894(left) or the same antibody preincubated with blocking peptide(right).](http://images.novusbio.com/fullsize/nb100-81894_rabbit-polyclonal-egfr-p-tyr1092-antibody-103202523464545.jpg)
![Western Blot: NPHP4 Antibody - BSA Free [NBP3-47314] - Mouse brain tissue were subjected to SDS PAGE followed by western blot with (NPHP4 antibody) at dilution of 1:600](http://images.novusbio.com/fullsize/nbp3-47314_rabbit-nphp4-pab-bsa-free-284202512315756.jpg "Western Blot: NPHP4 Antibody - BSA Free [NBP3-47314] - Mouse brain tissue were subjected to SDS PAGE followed by western blot with (NPHP4 antibody) at dilution of 1:600")
![Immunohistochemistry: NPHP4 Antibody - BSA Free [NBP3-47314] - Immunohistochemistry of paraffin-embedded human heart using (NPHP4 antibody) at dilution of 1:50](http://images.novusbio.com/fullsize/nbp3-47314_rabbit-nphp4-pab-bsa-free-28420251235688.jpg)
![Immunohistochemistry;RBX1 Antibody[NBP3-30392]Detection of human ROC1 by immunohistochemistry. Sample: FFPE section of human osteosarcoma. Antibody: Affinity purified rabbit anti-ROC1 used at a dilution of 1:1,000 . Detection: DAB](http://images.novusbio.com/fullsize/nbp3-30395_rabbit-rbx1-pab-78202410153536.jpg "Immunohistochemistry;RBX1 Antibody[NBP3-30392]Detection of human ROC1 by immunohistochemistry. Sample: FFPE section of human osteosarcoma. Antibody: Affinity purified rabbit anti-ROC1 used at a dilution of 1:1,000 . Detection: DAB")
![Immunohistochemistry;RBX1 Antibody[NBP3-30395]Detection of human ROC1 by immunohistochemistry. Sample: FFPE section of human ovarian carcinoma. Antibody: Affinity purified rabbit anti-ROC1 used at a dilution of 1:1,000 . Detection: DAB](http://images.novusbio.com/fullsize/nbp3-30395_rabbit-rbx1-pab-78202410153530.jpg)
![Western Blot: Chk2 [p Thr68] Antibody [NBP3-13076] - Untreated (-) and treated (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Chk2 (phospho Thr68) antibody (NBP3-13076) diluted at 1:1000.](http://images.novusbio.com/fullsize/Chk2-[p-Thr68]-Antibody-Western-Blot-NBP3-13076-img0001.jpg "<b>Biological Strategies Validation. </b>Western Blot: Chk2 [p Thr68] Antibody [NBP3-13076] - Untreated (-) and treated (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Chk2 (phospho Thr68) antibody (NBP3-13076) diluted at 1:1000.")
![<b>Biological Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: Chk2 [p Thr68] Antibody [NBP3-13076] - Chk2 (phospho Thr68) antibody detects Chk2 (phospho Thr68) protein at nucleus by immunofluorescent analysis. Sample: Mock and treated HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: Chk2 (phospho Thr68) stained by Chk2 (phospho Thr68) antibody (NBP3-13076) diluted at 1:500. Red: alpha Tubulin, a cytoskeleton marker, stained by alpha Tubulin antibody [GT114] (NBP2-43837) diluted at 1:500. Scale bar= 10 um.](http://images.novusbio.com/fullsize/Chk2-[p-Thr68]-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-13076-img0002.jpg)
![<b>Genetic Strategies Validation. </b>Knockout Validated: Chk2 [p Thr68] Antibody [NBP3-13076] - Wild-type (WT) and Chk2 (phospho Thr68) knockout (KO) HeLa cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Chk2 (phospho Thr68) antibody (NBP3-13076) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize/Chk2-[p-Thr68]-Antibody-Western-Blot-NBP3-13076-img0003.jpg)
![Immunoprecipitation: N-Cadherin Antibody [NBP3-14690] - Whole cell lysate (1.0 mgper IP reaction; 20% of IP loaded) from HeLa cells preparedusing NETN lysis buffer. Antibodies: Rabbit anti-NCadherin recombinant monoclonal antibody used for IP at 12 ul per reaction. NCadherin was also immunoprecipitated by rabbit anti-NCadherin antibody. For blottingimmunoprecipitated N-Cadherin, was used at1:1000. Chemiluminescence with an exposure time of 10seconds.](http://images.novusbio.com/fullsize/N-Cadherin-Antibody-Immunoprecipitation-NBP3-14690-img0001.jpg "Immunoprecipitation: N-Cadherin Antibody [NBP3-14690] - Whole cell lysate (1.0 mgper IP reaction; 20% of IP loaded) from HeLa cells preparedusing NETN lysis buffer. Antibodies: Rabbit anti-NCadherin recombinant monoclonal antibody used for IP at 12 ul per reaction. NCadherin was also immunoprecipitated by rabbit anti-NCadherin antibody. For blottingimmunoprecipitated N-Cadherin, was used at1:1000. Chemiluminescence with an exposure time of 10seconds.")
![Various whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with Hexokinase 2 antibody [HL2000] (NBP3-48667) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-48667_rabbit-hexokinase-2-mab-hl2000-western-blot-1411202518324118.jpg "Various whole cell extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with Hexokinase 2 antibody [HL2000] (NBP3-48667) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.")
![Non-transfected (-) and transfected (+) 293T whole cell extracts were separated by 5% SDS-PAGE, and the membrane was blotted with Hexokinase 2 antibody [HL2000] (NBP3-48667) diluted at 1:25000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-48667_rabbit-hexokinase-2-mab-hl2000-western-blot-1411202518443413.jpg)
![Zebrafish tissue extract (30 ug) was separated by 5% SDS-PAGE, and the membrane was blotted with Hexokinase 2 antibody [HL2000] (NBP3-48667) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp3-48667_rabbit-hexokinase-2-mab-hl2000-western-blot-141120251840430.jpg)
![Whole Japanese medaka extract (30 ug) was separated by 5% SDS-PAGE, and the membrane was blotted with Hexokinase 2 antibody [HL2000] (NBP3-48667) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize/nbp3-48667_rabbit-hexokinase-2-mab-hl2000-western-blot-141120251843314.jpg)
![Western Blot: Angiopoietin-1 Antibody (8H2) [NBP2-46519] - Human recombinant protein fragment corresponding to amino acids 198-498 of human ANGPT1 (NP_001137) produced in E.coli.](http://images.novusbio.com/fullsize/Angiopoietin-1-Antibody-8H2-Western-Blot-NBP2-46519-img0002.jpg "Western Blot: Angiopoietin-1 Antibody (8H2) [NBP2-46519] - Human recombinant protein fragment corresponding to amino acids 198-498 of human ANGPT1 (NP_001137) produced in E.coli.")
![Immunohistochemistry: Angiopoietin-1 Antibody (8H2) [NBP2-46519] - Analysis of Carcinoma of Human liver tissue.(Heat-induced epitope retrieval by 1 mM EDTA in 10mM Tris, pH8.5, 120C for 3min)](http://images.novusbio.com/fullsize/Angiopoietin-1-Antibody-8H2-Immunohistochemistry-NBP2-46519-img0001.jpg)