Parathyroid Gland Development Pathway Bioinformatics
Disease and disorder research has been conducted in relation to the Parathyroid Gland Development Pathway and Hypoparathyroidism, Parathyroid Neoplasms, Adenoma, Hypocalcemia, Parathyroid Diseases. The study of the Parathyroid Gland Development Pathway has been mentioned in research publications which can be found using our bioinformatics tool below. The Parathyroid Gland Development Pathway has been researched in relation to Gland Development, Cell Differentiation, Parathyroid Hormone Secretion, Glial Cell Differentiation, System Development. The Parathyroid Gland Development Pathway complements our catalog of research reagents including antibodies and ELISA kits against 25-HYDROXYVITAMIN D(3) 1-ALPHA-HYDROXYLASE, ALDH9A1, AIRE, CDR1, CYP27B1.
Top Research Reagents
We have 1366 products for the study of the Parathyroid Gland Development Pathway that can be applied to Chromatin Immunoprecipitation, Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
![Western Blot: Cullin 1 Antibody [NBP3-16092] - Western blot analysis of extracts of various cell lines, using Cullin 1 antibody (NBP3-16092) 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.](https://images.novusbio.com/fullsize/Cullin-1-Antibody-Western-Blot-NBP3-16092-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: Cullin 1 Antibody [NBP3-16092] - Immunofluorescence analysis of HeLa cells using Cullin 1 antibody (NBP3-16092). Blue: DAPI for nuclear staining.](https://images.novusbio.com/fullsize/Cullin-1-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-16092-img0001.jpg)
![Western Blot: GCM1 Antibody (2E11) [H00008521-M05] - Analysis of GCM1 expression in FHs 173 WE.](https://images.novusbio.com/fullsize/GCM1-Antibody-2E11-Western-Blot-H00008521-M05-img0008.jpg)
![Immunocytochemistry/Immunofluorescence: GCM1 Antibody (2E11) [H00008521-M05] - Analysis of monoclonal antibody to GCM1 on HeLa cell. Antibody concentration 10 ug/ml](https://images.novusbio.com/fullsize/GCM1-Antibody-2E11-Immunocytochemistry-Immunofluorescence-H00008521-M05-img0005.jpg)
![Western Blot: Autoimmune Regulator/AIRE Antibody [NB100-1063] - Staining of nuclear Jurkat cell with antibody at 1 ug/mL (A), Human Spleen with antibody at 2 ug/mL (B) and negative control Human Smooth Muscle (C) lysate (35 ug protein in RIPA buffer). Detected by chemiluminescence.](https://images.novusbio.com/fullsize/Autoimmune-Regulator-AIRE-Antibody-Western-Blot-NB100-1063-img0007.jpg)
![Immunocytochemistry/Immunofluorescence: Autoimmune Regulator/AIRE Antibody [NB100-1063] - Analysis of paraformaldehyde fixed HeLa cells, permeabilized with 0.15% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL), showing nucleoplasm and nuclear membrane staining. Actin filaments were stained with phalloidin (red) and the nuclear stain is DAPI (blue). Negative control: Unimmunized goat IgG (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (2 ug/mL).](https://images.novusbio.com/fullsize/Autoimmune-Regulator-AIRE-Antibody-Immunocytochemistry-Immunofluorescence-NB100-1063-img0011.jpg)
![Western Blot: GCM2 Antibody [NBP1-33040] - Sample (30 ug of whole cell lysate) A: A431 7. 5% SDS PAGE; antibody diluted at 1:1000.](https://images.novusbio.com/fullsize/GCM2-Antibody-Western-Blot-NBP1-33040-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: Factor IX Antibody [NBP1-33581] - HepG2 cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: Factor IX protein stained by Factor IX antibody [N3C3] diluted at 1:500. Blue: Hoechst 33342 staining.](https://images.novusbio.com/fullsize/Factor-IX-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-33581-img0005.jpg)
![Immunohistochemistry-Paraffin: Factor IX Antibody [NBP1-33581] - Mouse liver. Factor IX stained by Factor IX antibody [N3C3] diluted at 1:500.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min.](https://images.novusbio.com/fullsize/Factor-IX-Antibody-Immunohistochemistry-Paraffin-NBP1-33581-img0009.jpg)
![Immunohistochemistry-Paraffin: PTRH1 Antibody [NBP1-86713] - Staining of human soft tissue shows weak cytoplasmic positivity in adipocytes.](https://images.novusbio.com/fullsize/PTRH1-Antibody-Immunohistochemistry-Paraffin-NBP1-86713-img0001.jpg)
![Western Blot: ALDH9A1 Antibody [NBP1-89150] - Analysis in rat cell line NBT-II.](https://images.novusbio.com/fullsize/ALDH9A1-Antibody-Western-Blot-NBP1-89150-img0009.jpg)
![Immunohistochemistry-Paraffin: ALDH9A1 Antibody [NBP1-89150] - Staining of human liver shows strong cytoplasmic positivity in hepatocytes.](https://images.novusbio.com/fullsize/ALDH9A1-Antibody-Immunohistochemistry-Paraffin-NBP1-89150-img0002.jpg)
![Western Blot: Skp1 Antibody [NBP2-20380] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 15% SDS-PAGE, and the membrane was blotted with SKP1 antibody diluted at 1:500. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](https://images.novusbio.com/fullsize/Skp1-Antibody-Western-Blot-NBP2-20380-img0004.jpg)
![Immunohistochemistry-Paraffin: Skp1 Antibody [NBP2-20380] - Paraffin-embedded mouse middle brain. SKP1 antibody dilution: 1:500.](https://images.novusbio.com/fullsize/Skp1-Antibody-Immunohistochemistry-Paraffin-NBP2-20380-img0003.jpg)
![Western Blot: UBE3C Antibody [NBP2-20790] - Sample (50 ug of whole cell lysate) A: Mouse Brain, 5% SDS PAGE gel, diluted at 1:500.](https://images.novusbio.com/fullsize/UBE3C-Antibody-Western-Blot-NBP2-20790-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: UBE3C Antibody [NBP2-20790] - Immunofluorescence analysis of paraformaldehyde-fixed HeLa, using antibody at 1:500 dilution.](https://images.novusbio.com/fullsize/UBE3C-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-20790-img0003.jpg)
![Immunohistochemistry-Paraffin: HMBS Antibody [NBP2-33600] - Staining in human bone marrow and cerebral cortex tissues using anti-HMBS antibody. Corresponding HMBS RNA-seq data are presented for the same tissues.](https://images.novusbio.com/fullsize/HMBS-Antibody-Immunohistochemistry-Paraffin-NBP2-33600-img0012.jpg)
![Western Blot: HMBS Antibody [NBP2-33600] - Lane 1: Marker [kDa] 250, 130, 95, 72, 55, 36, 28, 17, 10<br/>Lane 2: Human cell line RT-4](https://images.novusbio.com/fullsize/HMBS-Antibody-Western-Blot-NBP2-33600-img0003.jpg)
![Western Blot: CDC73/HRPT2 Antibody [NB200-184] - Detection of Human and Mouse Para fibromin by Western Blot. Samples: Whole cell lysate (50 ug) from mouse TCMK-1 and human 293T cells. Antibodies: Affinity purified rabbit anti-Parafibromin antibody NB200-184 used for WB at 0.04 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.](https://images.novusbio.com/fullsize/CDC73-HRPT2-Antibody-Western-Blot-NB200-184-img0006.jpg)
![Immunoprecipitation: CDC73/HRPT2 Antibody [NB200-184] - Detection of human CDC73/HRPT2 (Parafibromin) by western blot of immunoprecipitates. Samples: Whole cell lysate (1 mg for IP; 20% of IP loaded) from HEK293T cells. Antibodies: Affinity purified rabbit anti-CDC73/HRPT2 antibody NB200-184 used for IP at 6 ug/mg lysate. For blotting immunoprecipitated CDC73/HRPT2, NB200-184 was used at 0.04 ug/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.](https://images.novusbio.com/fullsize/CDC73-HRPT2-Antibody-Immunoprecipitation-NB200-184-img0007.jpg)
![Simple Western: PCNA Antibody (PC10) [NB500-106] - Image shows a specific band for PCNA in 0.5 mg/mL of HeLa lysate. This experiment was performed under reducing conditions using the 12-230 kDa separation system.](https://images.novusbio.com/fullsize/PCNA-Antibody-PC10-Simple-Western-NB500-106-img0008.jpg)
![Immunocytochemistry/Immunofluorescence: PCNA Antibody (PC10) [NB500-106] - NIH3T3 cells were fixed and permeabilized for 10 minutes using -20C MeOH. The cells were incubated with anti-PCNA Antibody (PC10) NB500-106 at 1 ug/ml overnight at 4C and detected with an anti-mouse 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.](https://images.novusbio.com/fullsize/PCNA-Antibody-PC10-Immunocytochemistry-Immunofluorescence-NB500-106-img0015.jpg)
![Immunocytochemistry/Immunofluorescence: CDR1 Antibody [NBP2-57758] - Staining of human cell line BJ shows localization to nucleoplasm, the Golgi apparatus & centrosome. Antibody staining is shown in green.](https://images.novusbio.com/fullsize/CDR1-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-57758-img0001.jpg)
![Western Blot: VDR/NR1I1/Vitamin D Receptor Antibody (JA11-16) [NBP2-66778] - Western blot analysis of VDR/NR1I1/Vitamin D Receptor on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: MCF-7 cell lysate Lane 2: U937 cell lysate](https://images.novusbio.com/fullsize/VDR-NR1I1-Vitamin-D-Receptor-Antibody-JA11-16-Western-Blot-NBP2-66778-img0008.jpg)
![Immunohistochemistry-Paraffin: VDR/NR1I1/Vitamin D Receptor Antibody (JA11-16) [NBP2-66778] - Analysis of paraffin-embedded rat skin tissue with Rabbit anti-Vitamin D Receptor antibody washed with ddH2O and PBS, and then probed with the primary antibody at 1/800 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](https://images.novusbio.com/fullsize/VDR-NR1I1-Vitamin-D-Receptor-Antibody-JA11-16-Immunohistochemistry-Paraffin-NBP2-66778-img0010.jpg)
![Western Blot: FBXW2 Antibody [NB100-1300] - (0.3ug/ml) of Human Kidney lysate (RIPA buffer, 30ug total protein per lane). Primary incubated for 1 hour. Detected by western blot using chemiluminescence.](https://images.novusbio.com/fullsize/FBXW2-Antibody-Western-Blot-NB100-1300-img0002.jpg)
![Immunohistochemistry: FBXW2 Antibody [NB100-1300] - (3ug/ml) staining of paraffin embedded Human Kidney. Microwaved antigen retrieval with citrate buffer pH 6, HRP-staining.](https://images.novusbio.com/fullsize/FBXW2-Antibody-Immunohistochemistry-NB100-1300-img0001.jpg)
