TICRR Antibody - BSA Free
Novus Biologicals | Catalog # NBP2-41283
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Key Product Details
Species Reactivity
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Applications
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Label
Antibody Source
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Product Specifications
Immunogen
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Theoretical MW
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Scientific Data Images for TICRR Antibody - BSA Free
Western Blot: TICRR AntibodyBSA Free [NBP2-41283]
Western Blot: TICRR Antibody [NBP2-41283] - Western blot analysis of TICRR in human small intestine tissue lysate with TICRR antibody at 1 ug/ml.Immunohistochemistry: TICRR Antibody - BSA Free [NBP2-41283] -
Immunohistochemistry: TICRR Antibody - BSA Free [NBP2-41283] - Immunohistochemistry of TICRR in human small intestine tissue with TICRR antibody at 5 ug/mL.Immunocytochemistry/ Immunofluorescence: TICRR Antibody - BSA Free [NBP2-41283] -
Immunocytochemistry/ Immunofluorescence: TICRR Antibody - BSA Free [NBP2-41283] - Immunofluorescence of TICRR in human small intestine tissue with TICRR antibody at 20 ug/mL.Western Blot: TICRR Antibody - BSA Free [NBP2-41283] -
Knockdown of TICRR inhibited cell proliferation. (A)TICRR expression was inhibited in MCF7 cells using siRNA and shRNA. Efficiency of TICRR knockdown evaluated by RT-qPCR. Data were mean +/- SEM, N = 3 biological replicates. (B) Relative proliferation in control and TICRR-knockdown MCF7 cells after transfection for 48 h. Western blot (left) was performed. The proliferation in control cells was set at 1. *P < 0.05, two-tailed Student's t-test. Data were mean +/- SEM, N = 3 biological replicates. (C,D) Growth curves of TICRR-knockdown cells and control in MCF7 (C) and HCC1806 (D) cell lines. western blot (left) was performed. Cell viability at 0 h was set at 1. *P < 0.05, **p < 0.01, ****p < 1.0 × 10−4, two-way ANOVA test. Results were displayed as means +/- SEM, N = 3 biological replicates. (E,F) Knockdown of TICRR inhibited the colony formation in MCF7 (E) and HCC1806 (F) cells examined by plate colony formation assay. Representative colonies pictures were shown on the left and percentage of colony number were on the right. *P < 0.05, two-tailed Student's t-test. Results were displayed as means +/- SEM, N = 3 biological replicates. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/31275851), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: TICRR Antibody - BSA Free [NBP2-41283] -
Knockdown of TICRR inhibited cell proliferation. (A)TICRR expression was inhibited in MCF7 cells using siRNA and shRNA. Efficiency of TICRR knockdown evaluated by RT-qPCR. Data were mean +/- SEM, N = 3 biological replicates. (B) Relative proliferation in control and TICRR-knockdown MCF7 cells after transfection for 48 h. Western blot (left) was performed. The proliferation in control cells was set at 1. *P < 0.05, two-tailed Student's t-test. Data were mean +/- SEM, N = 3 biological replicates. (C,D) Growth curves of TICRR-knockdown cells and control in MCF7 (C) and HCC1806 (D) cell lines. western blot (left) was performed. Cell viability at 0 h was set at 1. *P < 0.05, **p < 0.01, ****p < 1.0 × 10−4, two-way ANOVA test. Results were displayed as means +/- SEM, N = 3 biological replicates. (E,F) Knockdown of TICRR inhibited the colony formation in MCF7 (E) and HCC1806 (F) cells examined by plate colony formation assay. Representative colonies pictures were shown on the left and percentage of colony number were on the right. *P < 0.05, two-tailed Student's t-test. Results were displayed as means +/- SEM, N = 3 biological replicates. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/31275851), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: TICRR Antibody - BSA Free [NBP2-41283] -
Knockdown of TICRR inhibited cell proliferation. (A)TICRR expression was inhibited in MCF7 cells using siRNA and shRNA. Efficiency of TICRR knockdown evaluated by RT-qPCR. Data were mean +/- SEM, N = 3 biological replicates. (B) Relative proliferation in control and TICRR-knockdown MCF7 cells after transfection for 48 h. Western blot (left) was performed. The proliferation in control cells was set at 1. *P < 0.05, two-tailed Student's t-test. Data were mean +/- SEM, N = 3 biological replicates. (C,D) Growth curves of TICRR-knockdown cells and control in MCF7 (C) and HCC1806 (D) cell lines. western blot (left) was performed. Cell viability at 0 h was set at 1. *P < 0.05, **p < 0.01, ****p < 1.0 × 10−4, two-way ANOVA test. Results were displayed as means +/- SEM, N = 3 biological replicates. (E,F) Knockdown of TICRR inhibited the colony formation in MCF7 (E) and HCC1806 (F) cells examined by plate colony formation assay. Representative colonies pictures were shown on the left and percentage of colony number were on the right. *P < 0.05, two-tailed Student's t-test. Results were displayed as means +/- SEM, N = 3 biological replicates. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/31275851), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Applications for TICRR Antibody - BSA Free
Immunocytochemistry/ Immunofluorescence
Immunohistochemistry
Immunohistochemistry-Paraffin
Western Blot
Formulation, Preparation, and Storage
Purification
Formulation
Format
Preservative
Concentration
Shipping
Stability & Storage
Background: TICRR
Alternate Names
Gene Symbol
Additional TICRR Products
Product Documents for TICRR Antibody - BSA Free
Certificate of Analysis
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Product Specific Notices for TICRR Antibody - BSA Free
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
Citations for TICRR Antibody - BSA Free
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- Antigen Retrieval Protocol (PIER)
- Antigen Retrieval for Frozen Sections Protocol
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- Chromogenic IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Chromogenic Immunohistochemistry Staining of Frozen Tissue
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- ELISA Sample Preparation & Collection Guide
- ELISA Troubleshooting Guide
- Fluorescent IHC Staining of Frozen Tissue Protocol
- Graphic Protocol for Heat-induced Epitope Retrieval
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Graphic Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- How to Run an R&D Systems DuoSet ELISA
- How to Run an R&D Systems Quantikine ELISA
- How to Run an R&D Systems Quantikine™ QuicKit™ ELISA
- ICC Cell Smear Protocol for Suspension Cells
- ICC Immunocytochemistry Protocol Videos
- ICC for Adherent Cells
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- Immunofluorescent IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunohistochemistry Frozen Troubleshooting
- Immunohistochemistry Paraffin Troubleshooting
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Making a 4% Formaldehyde Solution in PBS
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Fluorescent ICC Staining of Cell Smears - Graphic
- Protocol for the Fluorescent ICC Staining of Cultured Cells on Coverslips - Graphic
- Protocol for the Preparation & Fixation of Cells on Coverslips
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections - Graphic
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections - Graphic
- Protocol for the Preparation and Fluorescent ICC Staining of Cells on Coverslips
- Protocol for the Preparation and Fluorescent ICC Staining of Non-adherent Cells
- Protocol for the Preparation and Fluorescent ICC Staining of Stem Cells on Coverslips
- Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- Protocol for the Preparation of a Cell Smear for Non-adherent Cell ICC - Graphic
- Quantikine HS ELISA Kit Assay Principle, Alkaline Phosphatase
- Quantikine HS ELISA Kit Principle, Streptavidin-HRP Polymer
- R&D Systems Quality Control Western Blot Protocol
- Sandwich ELISA (Colorimetric) – Biotin/Streptavidin Detection Protocol
- Sandwich ELISA (Colorimetric) – Direct Detection Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: ELISA
- Troubleshooting Guide: Immunohistochemistry
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars