Rabbit Polyclonal TBC1D15 antibody. Suitable for IHC-P, ICC/IF, WB and reacts with Human, Mouse, Rat samples. Cited in 4 publications. Immunogen corresponding to Recombinant Fragment Protein within Human TBC1D15 aa 150-300.
pH: 7.2
Preservative: 0.02% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine)
IHC-P | ICC/IF | WB | |
---|---|---|---|
Human | Tested | Tested | Tested |
Mouse | Expected | Expected | Tested |
Rat | Expected | Expected | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/20.00000 - 1/50.00000 | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 0.25000-2.00000 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 0.04000-0.40000 µg/mL | Notes - |
Species Rat | Dilution info 0.04000-0.40000 µg/mL | Notes - |
Species Human | Dilution info 0.04000-0.40000 µg/mL | Notes - |
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Acts as a GTPase activating protein for RAB7A. Does not act on RAB4, RAB5 or RAB6 (By similarity).
TBC1 domain family member 15, GTPase-activating protein RAB7, GAP for RAB7, Rab7-GAP, TBC1D15
Rabbit Polyclonal TBC1D15 antibody. Suitable for IHC-P, ICC/IF, WB and reacts with Human, Mouse, Rat samples. Cited in 4 publications. Immunogen corresponding to Recombinant Fragment Protein within Human TBC1D15 aa 150-300.
pH: 7.2
Preservative: 0.02% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine)
TBC1D15 also known as TBC1 Domain Family Member 15 is a Rab GTPase-activating protein (Rab-GAP) with a molecular mass of approximately 72 kDa. This protein predominantly functions to regulate intracellular membrane trafficking by inactivating Rab GTPases such as Rab7 and Rab36. These Rab GTPases play essential roles in various cellular processes including endocytosis and vesicular trafficking. TBC1D15 is widely expressed in various tissues but demonstrated higher levels in the brain and skeletal muscle indicating tissue-specific roles or regulation.
TBC1D15 contributes to mitochondrial dynamics and autophagy processes. It functions as part of a complex with the fission protein Fis1 on the mitochondrial outer membrane. By binding to Fis1 TBC1D15 plays an important role in mediating mitochondrial fission. This activity is interconnected with cellular energy homeostasis and quality control reflecting its influence on cellular health and survival. In the context of autophagy TBC1D15 regulation appears to ensure proper cargo selection and vesicle trafficking efficiency essential steps in cellular waste management.
TBC1D15 participates in the mitophagy pathway and endocytic recycling pathway. The mitophagy pathway involves the removal of damaged mitochondrian important for cellular homeostasis and metabolism where TBC1D15 interacts with proteins such as Fis1 and Drp1 to facilitate mitochondrial division. In the endocytic recycling pathway TBC1D15 associates with Rab7 an important player in lysosome function and autophagy affecting cargo sorting and membrane turnover which are necessary for maintaining cellular balance and adapting to stress.
Changes in TBC1D15 activity have been linked to neurodegenerative conditions including Parkinson's disease and Alzheimer's disease. These diseases often feature mitochondrial dysfunction and defective autophagy processes in which TBC1D15 plays a significant role. Aberrations in its interaction with proteins like Rab7 and Fis1 may contribute to the pathological environment seen in these diseases emphasizing its potential as a therapeutic target or biomarker for mitochondrial-related pathologies.
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Immunohistochemical analysis of paraffin embedded human kidney tissue labeling TBC1D15 with ab121396 antibody at a 1/20 dilution.
Performed heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
Immunofluorescent staining of Human cell line U-2 OS shows positivity in cytoplasm and mitochondria. Recommended concentration of ab121396 1-4 µg/ml. Cells treated with PFA/Triton X-100.
All lanes: Western blot - Anti-TBC1D15 antibody (ab121396) at 0.4 µg/mL
Lane 1: NIH/3T3 (mouse embryo fibroblast cell line) cell lysate
Lane 2: NBT-II (rat urinary bladder tumor cell line) cell lysate
Predicted band size: 79 kDa
Immunohistochemical analysis of paraffin embedded human testis tissue labeling TBC1D15 with ab121396 antibody at a 1/20 dilution.
Performed heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
Immunohistochemical analysis of paraffin embedded human placenta tissue labeling TBC1D15 with ab121396 antibody at a 1/20 dilution.
Performed heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
Immunohistochemical analysis of paraffin embedded human skin tissue labeling TBC1D15 with ab121396 antibody at a 1/20 dilution.
Performed heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
All lanes: Western blot - Anti-TBC1D15 antibody (ab121396) at 0.4 µg/mL
All lanes: NTERA-2 (human malignant pluripotent embryonic carcinoma cell line) cell lysate
Predicted band size: 79 kDa
Western blot: Rabbit Polyclonal to TBC1D15 ab121396 staining at 0.1 µg/mL, shown in green; Mouse anti GAPDH (Anti-GAPDH antibody [6C5] - Loading Control ab8245) loading control staining at 1/20,000 dilution, shown in magenta. A band was observed at 75 kDa in Wild-type A549 ab288558 cell lysates with no signal observed at this size in TBC1D15 knockout A549 cell line. To generate this image, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3pc Milk in TBS-0.1 % Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit 800CW & Goat anti-Mouse 680RD at 1/20,000 dilution.
All lanes: Western blot - Anti-TBC1D15 antibody (ab121396) at 0.1 µg/mL
Lane 1: Wild-type A549 ab288558 at 20 µg
Lane 2: TBC1D15 knockout A549 at 20 µg
Lane 3: HeLa at 20 µg
Lane 4: A549 Nuclear at 20 µg
All lanes: Goat anti-Rabbit 800CW & Goat anti-Mouse 680RD at 1/20000 dilution
Performed under reducing conditions.
Predicted band size: 79 kDa
Observed band size: 75 kDa
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