Rabbit Polyclonal REEP3 antibody. Suitable for WB and reacts with Rat samples. Cited in 3 publications. Immunogen corresponding to Synthetic Peptide within Human REEP3.
pH: 7.2
Preservative: 0.02% Sodium azide
Constituents: 99% PBS
WB | |
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Rat | Tested |
Species | Dilution info | Notes |
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Species Rat | Dilution info 1.00000-2.00000 µg/mL | Notes - |
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Microtubule-binding protein required to ensure proper cell division and nuclear envelope reassembly by sequestering the endoplasmic reticulum away from chromosomes during mitosis. Probably acts by clearing the endoplasmic reticulum membrane from metaphase chromosomes.
C10orf74, REEP3, Receptor expression-enhancing protein 3
Rabbit Polyclonal REEP3 antibody. Suitable for WB and reacts with Rat samples. Cited in 3 publications. Immunogen corresponding to Synthetic Peptide within Human REEP3.
pH: 7.2
Preservative: 0.02% Sodium azide
Constituents: 99% PBS
At least three isoforms of REEP3 are known to exist; ab106463 will detect all three.
ab106463 was purified by affinity chromatography via a peptide column.
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REEP3 also known as Receptor Accessory Protein 3 plays an important role in mechanical processes within the cell. This protein assists in shaping the endoplasmic reticulum (ER) by facilitating the stacking and proper organization of the ER membranes. REEP3 has a molecular weight of approximately 28 kDa. Its expression is widespread but shows significant presence in neuronal tissues suggesting a specialized role in these cells.
REEP3 manages the structural integrity of the endoplasmic reticulum by interacting with other proteins involved in ER morphology. It forms part of a complex that includes microtubule-associated proteins which link the ER to the cytoskeleton enabling proper cellular function. Through this interaction REEP3 supports the maintenance of cellular homeostasis and can influence processes such as protein synthesis and transport.
Proteins like REEP3 contribute to ER shaping pathways and cellular stress response mechanisms. It acts alongside proteins like ATLASTIN and SEIPIN in the ER network assembly. Specifically it connects with pathways managing ER stress responses which are vital in adapting to and regulating changes in protein folding demand.
Aberrations in REEP3 function associate with conditions affecting the nervous system such as hereditary spastic paraplegia (HSP). Mutations in REEP3 can lead to defects in ER morphology contributing to neurodegenerative processes. The protein interacts with SPG4 and REEP1 linking it to cytoskeletal abnormalities observed in these disorders. Understanding REEP3's precise role in these pathologies offers potential avenues for therapeutic intervention.
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All lanes: Western blot - Anti-REEP3 antibody (ab106463) at 1 µg/mL
Lane 1: Rat heart tissue lysate at 15 µg
Lane 2: Rat heart tissue lysate at 15 µg with immunizing peptide
Predicted band size: 29 kDa
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