Rabbit Polyclonal PDE6D antibody. Suitable for ICC, WB, ICC/IF, IHC-Fr and reacts with Mouse, Pig, Human, Dog, Cow, Sheep samples. Cited in 4 publications.
IgG
Rabbit
Preservative: 0.05% Sodium azide
Constituents: 99% PBS, 0.1% BSA
Liquid
Polyclonal
ICC | WB | ICC/IF | IHC-Fr | |
---|---|---|---|---|
Human | Expected | Expected | Predicted | Expected |
Mouse | Expected | Expected | Tested | Expected |
Cow | Expected | Expected | Tested | Expected |
Dog | Expected | Expected | Predicted | Expected |
Pig | Expected | Expected | Predicted | Expected |
Sheep | Expected | Expected | Predicted | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Pig, Human, Dog, Cow, Sheep | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Pig, Human, Dog, Cow, Sheep | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/10.00000 - 1/200.00000 | Notes - |
Species Cow | Dilution info 1/10.00000 - 1/200.00000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Pig, Sheep, Dog | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes Immunohistochemical staining of PDE6D in bovine retinal cross-sections using ab5665 results in staining of retinal outer segments. |
Species Pig | Dilution info - | Notes Immunohistochemical staining of PDE6D in bovine retinal cross-sections using ab5665 results in staining of retinal outer segments. |
Species Human | Dilution info - | Notes Immunohistochemical staining of PDE6D in bovine retinal cross-sections using ab5665 results in staining of retinal outer segments. |
Species Dog | Dilution info - | Notes Immunohistochemical staining of PDE6D in bovine retinal cross-sections using ab5665 results in staining of retinal outer segments. |
Species Cow | Dilution info - | Notes Immunohistochemical staining of PDE6D in bovine retinal cross-sections using ab5665 results in staining of retinal outer segments. |
Species Sheep | Dilution info - | Notes Immunohistochemical staining of PDE6D in bovine retinal cross-sections using ab5665 results in staining of retinal outer segments. |
Select an associated product type
GMP-PDE delta, Pde6d
Rabbit Polyclonal PDE6D antibody. Suitable for ICC, WB, ICC/IF, IHC-Fr and reacts with Mouse, Pig, Human, Dog, Cow, Sheep samples. Cited in 4 publications.
IgG
Rabbit
Preservative: 0.05% Sodium azide
Constituents: 99% PBS, 0.1% BSA
Liquid
Polyclonal
Affinity purification Immunogen
This antibody does not detect other PDE6 isoforms.
Blue Ice
1-2 weeks
+4°C
-20°C
Upon delivery aliquot
Avoid freeze / thaw cycle
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This supplementary information is collated from multiple sources and compiled automatically.
The PDE6D protein also known as Phosphodiesterase Delta or PDE6 delta serves a mechanical function as a prenyl-binding protein. It facilitates the release of prenylated proteins from cellular membranes allowing their proper trafficking within the cell. PDE6D has a molecular mass of approximately 17 kDa and is a part of the larger phosphodiesterase family. Expression of this target occurs mainly in retinal photoreceptor cells but is also found in several other tissues such as the brain and kidneys.
PDE6D plays a role in the proper localization and function of various prenylated proteins contributing to retinal function. It is important for ciliary targeting allowing proteins like the small GTPase Ras and the retinitis pigmentosa protein RPGR to localize correctly. PDE6D itself does not form part of a larger complex but facilitates the interaction between proteins and other cell components ensuring that cellular processes proceed as needed.
PDE6D functions as an important player in small GTPase-mediated signal transduction. This protein interacts with the Ras superfamily of small GTPases important for intracellular signaling pathways. It plays a role in processes such as cell growth differentiation and apoptosis. The proper functioning of PDE6D ensures that prenylated proteins like Ras which are also implicated in these pathways are effectively transported to their destinations within the cell.
PDE6D has been linked to retinitis pigmentosa a degenerative eye disease leading to retinal dysfunction. Mutations in the PDE6D gene disrupt the proper trafficking of prenylated proteins including RPGR which is essential for photoreceptor cell survival and function. Additionally PDE6D may also play a role in Joubert syndrome where it affects the localization of proteins necessary for proper ciliary function contributing to the disorders observed in this syndrome.
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This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
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Immunocytochemistry/Immunofluorescence analysis of PDE6D (green) showing staining in the cytoplasm and nucleus of B-3 cells (right) compared to a negative control without primary antibody (left). Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were incubated with ab5565 in 3% BSA-PBS at a dilution of 1:100 and incubated overnight at 4 °C in a humidified chamber. Cells were washed with PBST and incubated with a DyLight-conjugated secondary antibody in PBS at room temperature in the dark. F-actin (red) was stained with a fluorescent red phalloidin and nuclei (blue) were stained with Hoechst or DAPI. Images were taken at a magnification of 60x.
Immunocytochemistry/Immunofluorescence analysis of PDE6D (green) showing staining in the cytoplasm and nucleus of BAEC cells (right) compared to a negative control without primary antibody (left). Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were incubated with ab5665 in 3% BSA-PBS at a dilution of 1:100 and incubated overnight at 4 °C in a humidified chamber. Cells were washed with PBST and incubated with a DyLight-conjugated secondary antibody in PBS at room temperature in the dark. F-actin (red) was stained with a fluorescent red phalloidin and nuclei (blue) were stained with Hoechst or DAPI. Images were taken at a magnification of 60x.
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