Rabbit Polyclonal GMAP-210 antibody. Suitable for IHC-P, ICC/IF and reacts with Human samples. Immunogen corresponding to Recombinant Fragment Protein within Human TRIP11 aa 1-150.
pH: 7.2
Preservative: 0.02% Sodium azide
Constituents: PBS, 40% Glycerol (glycerin, glycerine)
IHC-P | ICC/IF | |
---|---|---|
Human | Tested | Tested |
Pig | Predicted | Predicted |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/50.00000 - 1/200.00000 | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Pig | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1.00000-4.00000 µg/mL | Notes Fixation/Permeabilization: PFA/Triton X-100. |
Species | Dilution info | Notes |
---|---|---|
Species Pig | Dilution info - | Notes - |
Is a membrane tether required for vesicle tethering to Golgi. Has an essential role in the maintenance of Golgi structure and function (PubMed:25473115, PubMed:30728324). It is required for efficient anterograde and retrograde trafficking in the early secretory pathway, functioning at both the ER-to-Golgi intermediate compartment (ERGIC) and Golgi complex (PubMed:25717001). Binds the ligand binding domain of the thyroid receptor (THRB) in the presence of triiodothyronine and enhances THRB-modulated transcription.
CEV14, TRIP11, Thyroid receptor-interacting protein 11, TR-interacting protein 11, TRIP-11, Clonal evolution-related gene on chromosome 14 protein, Golgi-associated microtubule-binding protein 210, Trip230, GMAP-210
Rabbit Polyclonal GMAP-210 antibody. Suitable for IHC-P, ICC/IF and reacts with Human samples. Immunogen corresponding to Recombinant Fragment Protein within Human TRIP11 aa 1-150.
pH: 7.2
Preservative: 0.02% Sodium azide
Constituents: PBS, 40% Glycerol (glycerin, glycerine)
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GMAP-210 also known as Trip11 is a large coiled-coil protein with a molecular weight of approximately 228 kDa. It primarily functions as a Golgi microtubule-associated protein playing a role in the structural integrity and organization of the Golgi apparatus. This protein is expressed in cells across various tissues highlighting its important role in maintaining proper cellular operations.
GMAP-210 assists in vesicle tethering and trafficking processes ensuring the effective movement of proteins and lipids along the secretory pathway. It is not part of any large protein complex but interacts with other Golgi-associated proteins to stabilize microtubules and Golgi membranes. Its interactions are key for the correct sorting and delivery of proteins to their destinations within cells making it integral to maintaining cellular membrane dynamics.
GMAP-210 functions significantly within the secretory pathway. It interacts with proteins essential for Golgi transport such as Golgin-84 to mediate the movement of vesicles between the Golgi stacks and other cellular compartments. Additionally GMAP-210 has roles in the regulation of the microtubule network which is vital for intracellular transport and cellular morphology maintenance.
Defects in the GMAP-210 protein are linked to achondrogenesis type 1A and can also contribute to other skeletal dysplasias. It is associated with collagen processing errors due to its role in Golgi transport which can lead to structural protein accumulation. These disorders highlight the importance of GMAP-210's interaction with proteins like collagen in maintaining normal skeletal development and function.
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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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PFA-fixed, Triton X-100 permeabilized U-251 MG (human brain glioma cell line) cells stained for GMAP-210 (green) using ab251664 at 4 μg/ml in ICC/IF.
Paraffin-embedded human pancreas tissue stained for GMAP-210 using ab251664 at 1/50 dilution in immunohistochemical analysis.
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