TRIM30 Antibody - BSA Free
Novus Biologicals | Catalog # NBP2-41087
Key Product Details
Species Reactivity
Validated:
Mouse, Rat
Cited:
Mouse
Applications
Validated:
Immunohistochemistry, Immunohistochemistry-Paraffin, Immunohistochemistry-Frozen, Western Blot, ELISA, Immunocytochemistry/ Immunofluorescence
Cited:
Immunohistochemistry-Frozen, Western Blot, Immunocytochemistry/ Immunofluorescence, IF/IHC
Label
Unconjugated
Antibody Source
Polyclonal Rabbit IgG
Format
BSA Free
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Product Specifications
Immunogen
Antibody was raised against a 21 amino acid synthetic peptide near the amino terminus of the mouse TRIM30. The immunogen is located within amino acids 110 - 160 of TRIM30. Amino Acid Squence: RSQEHRGHQTALIEEVDQEYK
Reactivity Notes
Immunogen displays the following percentage of sequence identity for non-tested species: Human (80%)
Clonality
Polyclonal
Host
Rabbit
Isotype
IgG
Theoretical MW
105 kDa.
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.
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 TRIM30 Antibody - BSA Free
Western Blot: TRIM30 AntibodyBSA Free [NBP2-41087]
Western Blot: TRIM30 Antibody [NBP2-41087] - Analysis of TRIM30 in mouse heart tissue lysate with TRIM30 antibody at (A) 1 and (B) 2 ug/mL.Immunohistochemistry: TRIM30 Antibody - BSA Free [NBP2-41087] -
Immunohistochemistry: TRIM30 Antibody - BSA Free [NBP2-41087] - Immunohistochemistry of TRIM30 in mouse ovary tissue with TRIM30 antibody at 10 u/mL.Immunocytochemistry/ Immunofluorescence: TRIM30 Antibody - BSA Free [NBP2-41087] -
Immunocytochemistry/ Immunofluorescence: TRIM30 Antibody - BSA Free [NBP2-41087] - Immunofluorescence of TRIM30 in Human Ovary cells with TRIM30 antibody at 20 ug/mL.Western Blot: TRIM30 Antibody - BSA Free [NBP2-41087] -
Trim30a is upregulated by H. pylori in a STING-dependent manner. Murine gastric organoid monolayers or bone marrow derived dendritic cells (BMDC) derived from wild-type (WT) C57BL/6 or Sting−/− mice were challenged with PBS alone (UI) or wild-type (wt) H. pylori strain J166 or PMSS1 at MOI 100:1 for 24 hours. (a) Trim30a was quantified by Western blot analysis in co-cultured murine gastric organoid. Representative Western blots and densitometric analysis normalizing levels of Trim30a to Gapdh. (b) RT-PCR analysis of Trim30a mRNA levels in uninfected and H. pylori-infected wild-type and Sting−/− BMDCs. Data are represented as relative gene expression normalized to levels of Gapdh gene expression. (c) Trim30a was quantified by Western blot analysis in co-cultured BMDCs. Representative Western blots and densitometric analysis normalizing levels of Trim30a to Gapdh. In each experiment, conditions were tested at least 3 times and student’s t-tests were used to determine statistical significance between groups. *p <.05, **p <.01, ns = not significant. ##p <.01, ###p <.001 ####p <.0001 compared to untreated. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/35905376), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: TRIM30 Antibody - BSA Free [NBP2-41087] -
Trim30a is upregulated by H. pylori in a STING-dependent manner. Murine gastric organoid monolayers or bone marrow derived dendritic cells (BMDC) derived from wild-type (WT) C57BL/6 or Sting−/− mice were challenged with PBS alone (UI) or wild-type (wt) H. pylori strain J166 or PMSS1 at MOI 100:1 for 24 hours. (a) Trim30a was quantified by Western blot analysis in co-cultured murine gastric organoid. Representative Western blots and densitometric analysis normalizing levels of Trim30a to Gapdh. (b) RT-PCR analysis of Trim30a mRNA levels in uninfected and H. pylori-infected wild-type and Sting−/− BMDCs. Data are represented as relative gene expression normalized to levels of Gapdh gene expression. (c) Trim30a was quantified by Western blot analysis in co-cultured BMDCs. Representative Western blots and densitometric analysis normalizing levels of Trim30a to Gapdh. In each experiment, conditions were tested at least 3 times and student’s t-tests were used to determine statistical significance between groups. *p <.05, **p <.01, ns = not significant. ##p <.01, ###p <.001 ####p <.0001 compared to untreated. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/35905376), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Applications for TRIM30 Antibody - BSA Free
Application
Recommended Usage
Immunocytochemistry/ Immunofluorescence
20 ug/ml
Immunohistochemistry
10 ug/ml
Western Blot
1-2 ug/ml
Application Notes
Use in Immunohistochemistry-Frozen reported in scientific literature (PMID: 29079839).
Formulation, Preparation, and Storage
Purification
Peptide affinity purified
Formulation
PBS
Format
BSA Free
Preservative
0.02% Sodium Azide
Concentration
1 mg/ml
Shipping
The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Background: TRIM30
Alternate Names
Rpt1, Rpt-1, Trim30a
Additional TRIM30 Products
Product Documents for TRIM30 Antibody - BSA Free
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Product Specific Notices for TRIM30 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 TRIM30 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
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