TGN38 (Trans-Golgi network integral membrane protein TGN38) is an 80-100 kDa integral membrane protein that is associated with intracellular trafficking. Its name derives from the fact that its predicted MW is 38 kDa. Although TGN38 cycles continuously between the Golgi and plasma membrane via endosomal vesicles, it is principally localized to the Golgi apparatus. Functionally, TGN38 is involved in both the formation of secretory vesicles, and in the process of clathrin-mediated endocytosis. This is accomplished through the creation of a 250 kDa cytoplasmic complex composed of a Tgoln1 dimer, Rab6, and other molecules that interact with the F-actin binding proteins neurabin-I and -II. This interaction likely contributes to directional vesicle trafficking. Mature rat Tgoln1 is a type I transmembrane glycoprotein that is 340 amino acids (aa) in length. It contains a 286 aa extracellular/luminal region (aa 18-303) plus a 33 aa cytoplasmic domain (aa 325-357). The luminal region appears to be heavily glycosylated with both O- and N-linked carbohydrate, some of which terminates in polysialylation; the cytoplasmic domain contains a cytosolic trafficking motif that encompases aa 348-353. There is one splice variant (TGN41) that contains a 26 aa substitution for the three C-terminal aa of TGN38. It has been suggested that this may heterodimerize with TGN38. Over aa 18-303, rat TGN38/Tgoln1 shares 67% aa sequence identity with the mouse ortholog to rat Tgoln1.
Scientific images may be resized, cropped, or adjusted for brightness or contrast for presentation purposes. These updates are limited to presentation and do not affect the underlying scientific interpretation of the data. Where available, additional source data may be provided upon request.
Key Product Details
Species Reactivity
Applications
Label
Antibody Source
Product Specifications
Immunogen
Leu18-Ser303
Accession # P19814
Specificity
Clonality
Host
Isotype
Scientific Data Images for Rat TGN38 Antibody
Detection of Rat TGN38 by Western Blot.
Western blot shows lysates of RBL-2H3 rat basophilic leukemia cell line. PVDF membrane was probed with 0.25 µg/mL of Sheep Anti-Rat TGN38 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF8059) followed by HRP-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # HAF016). A specific band was detected for TGN38 at approximately 90 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.TGN38 in RBL-2H3 Rat Cell Line.
TGN38 was detected in immersion fixed RBL-2H3 rat basophilic leukemia cell line using Sheep Anti-Rat TGN38 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF8059) at 1.7 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Sheep IgG Secondary Antibody (red; Catalog # NL010) and counterstained with DAPI (blue). Specific staining was localized to Golgi vesicles in cytoplasm. View our protocol for Fluorescent ICC Staining of Non-adherent Cells.Detection of TGN38 by Immunohistochemistry
DARS2 depletion causes gradual Golgi disorganisation in proximal enterocytes that precedes LD formation and requires the presence of fat in the diet.a, Representative fluorescence microscopy images from the proximal SI of 8-12-week-old Dars2fl/fl (n = 6) and DARS2tamIEC-KO (n = 6) mice sacrificed 3, 5 and 8 days upon the last tamoxifen injection and immunostained with antibodies against TGN38 (red) and E-cadherin (green). Insets shows only TGN38 staining in white. b, Representative fluorescence microscopy images from the proximal and distal SI of 8-12-week-old Dars2fl/fl (n = 6) and DARS2tamIEC-KO (n = 6) mice fed with NCD sacrificed 3 and 8 days upon the last tamoxifen injection and immunostained with antibodies against TGN38 (red), E-cadherin (green) and PLIN2 (yellow). c, Representative fluorescence microscopy images from the proximal SI of 8-12-week-old Dars2fl/fl (n = 6) and DARS2tamIEC-KO (n = 6) mice under NCD and FFD sacrificed 7 days upon the last tamoxifen injection and immunostained with antibodies against TGN38 (red), E-cadherin (green) and PLIN2 (yellow). Nuclei stained with DAPI (blue). Scale bars, 50 μm. Confocal images shown are representative of the number of mice analysed as indicated in Supplementary Table 4. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/38123683), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of TGN38 by Immunohistochemistry
DARS2 depletion causes gradual Golgi disorganisation in proximal enterocytes that precedes LD formation and requires the presence of fat in the diet.a, Representative fluorescence microscopy images from the proximal SI of 8-12-week-old Dars2fl/fl (n = 6) and DARS2tamIEC-KO (n = 6) mice sacrificed 3, 5 and 8 days upon the last tamoxifen injection and immunostained with antibodies against TGN38 (red) and E-cadherin (green). Insets shows only TGN38 staining in white. b, Representative fluorescence microscopy images from the proximal and distal SI of 8-12-week-old Dars2fl/fl (n = 6) and DARS2tamIEC-KO (n = 6) mice fed with NCD sacrificed 3 and 8 days upon the last tamoxifen injection and immunostained with antibodies against TGN38 (red), E-cadherin (green) and PLIN2 (yellow). c, Representative fluorescence microscopy images from the proximal SI of 8-12-week-old Dars2fl/fl (n = 6) and DARS2tamIEC-KO (n = 6) mice under NCD and FFD sacrificed 7 days upon the last tamoxifen injection and immunostained with antibodies against TGN38 (red), E-cadherin (green) and PLIN2 (yellow). Nuclei stained with DAPI (blue). Scale bars, 50 μm. Confocal images shown are representative of the number of mice analysed as indicated in Supplementary Table 4. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/38123683), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Rat TGN38 Antibody
Immunocytochemistry
Sample: Immersion fixed RBL-2H3 rat basophilic leukemia cell line
Western Blot
Sample: RBL‑2H3 rat basophilic leukemia cell line
Formulation, Preparation, and Storage
Purification
Reconstitution
Reconstitute at 0.2 mg/mL in sterile PBS. For liquid material, refer to CoA for concentration.
Formulation
Shipping
Stability & Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Calculators
Background: TGN38
Long Name
Alternate Names
Gene Symbol
UniProt
Additional TGN38 Products
Product Documents for Rat TGN38 Antibody
Certificate of Analysis
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Note: Certificate of Analysis not available for kit components.
Product Specific Notices for Rat TGN38 Antibody
For research use only
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- ICC Cell Smear Protocol for Suspension Cells
- ICC Immunocytochemistry Protocol Videos
- ICC for Adherent Cells
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- 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 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 of a Cell Smear for Non-adherent Cell ICC - Graphic
- R&D Systems Quality Control Western Blot Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- 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