Prostaglandin-H2 D-isomerase, 0.1 mg

FOR RESEARCH USE ONLY.

Related Product Names:
- PTGDS protein; PTGDS; PDS; PGD2; PGDS; Prostaglandin-H2 D-isomerase
- EC 5.3.99.2; Lipocalin-type prostaglandin-D synthase; Glutathione-independent PGD synthetase; Prostaglandin-D2 synthase; PGD2 synthase; PGDS2; PGDS; Beta-trace protein; Cerebrin-28; Prostaglandin D2 synthase 21kDa (brain); prostaglandin D2 synthase (21kD, brain)

Fusion: T7 tag at N-terminus.
Source/Host: E Coli
Purity/Purification: 95%
Crossreactivity: human
Format: 10 mM Tris, pH 8.0, 0.1% Triton X-100, 0.002% NaN3.
Storage: -70 degree C. Avoid frequent freeze and thaw.
Stability: 6-12 months at -70 degree C.
Shipping: Products may be shipped on ice pack or dry ice.

Synonym Names for PTGDS protein: PTGDS; PDS; PGD2; PGDS; EC 5.3.99.2; Lipocalin-type prostaglandin-D synthase; Glutathione-independent PGD synthetase; Prostaglandin-D2 synthase; PGD2 synthase; PGDS2; PGDS; Beta-trace protein; Cerebrin-28; Prostaglandin D2 synthase 21kDa (brain); prostaglandin D2 synthase (21kD, brain)

Function: Catalyzes the conversion of PGH2 to PGD2, a prostaglandin involved in smooth muscle contraction/relaxation and a potent inhibitor of platelet aggregation. Involved in a variety of CNS functions, such as sedation, NREM sleep and PGE2-induced allodynia, and may have an anti-apoptotic role in oligodendrocytes. Binds small non-substrate lipophilic molecules, including biliverdin, bilirubin, retinal, retinoic acid and thyroid hormone, and may act as a scavenger for harmful hydrophopic molecules and as a secretory retinoid and thyroid hormone transporter. Possibly involved in development and maintenance of the blood-brain, blood-retina, blood-aqueous humor and blood-testis barrier. It is likely to play important roles in both maturation and maintenance of the central nervous system and male reproductive system.

Catalytic Activity: (5Z,13E)-(15S)-9-alpha,11-alpha-epidioxy-15-hydroxyprosta-5,13-dienoate = (5Z,13E)-(15S)-9-alpha,15-dihydroxy-11-oxoprosta-5,13-dienoate.

Subcellular Location: Endoplasmic reticulum; rough endoplasmic reticulum. Detected on rough endoplasmic reticulum of arachnoid and menigioma cells. Nucleus; nuclear membrane. Golgi apparatus. Localized to the nuclear envelope, Golgi apparatus, secretory vesicles and spherical cytoplasmic structures in arachnoid trabecular cells, and to circular cytoplasmic structures in meningeal macrophages and perivascular microglial cells. In oligodendrocytes, localized to the rough endoplasmic reticulum and nuclear envelope. Cytoplasm; perinuclear region. In retinal pigment epithelial cells, localized to distinct cytoplasmic domains including the perinuclear region. Secreted protein. Also secreted.

Tissue Specificity: Abundant in the brain and CNS where it is expressed in tissues of the blood-brain barrier and secreted into the cerebro-spinal fluid. Abundantly expressed in the heart. In the male reproductive system, it is expressed in the testis, epididymis and prostate, and is secreted into the seminal fluid. Expressed in the eye and secreted into the aqueous humor. Lower levels detected in various tissue fluids such as serum, normal urine, ascitic fluid and tear fluid. Also found in a number of other organs including ovary, fimbriae of the fallopian tubes, kidney, leukocytes.

Induction: By IL-1 beta and thyroid hormone. Probably induced by dexamethasone, dihydrotestosterone, progesterone, retinoic acid and retinal. Repressed by the Notch-Hes signaling pathway.

Ptm: Both N-glycosylation recognition sites are almost quantitatively occupied by N-glycans of the biantennary complex type, with a considerable proportion of structures bearing a bisecting GlcNAc. Agalacto structure as well as sialylated and nonsialylated oligosaccharides bearing alpha2-3- and/or alpha2-6-linked NeuNAc are present.

Miscellaneous: It has been proposed that the urinary and serum levels may provide a sensitive indicator of renal damage in diabetes mellitus and hypertension. Elevated levels in the coronary circulation may also be associated with angina. Changes in charge and molecular weight microheterogeneity, due to modification of the N-linked oligosaccharides, may be associated with neurodegenerative disease and multiple sclerosis. Detected in meningioma but not in other brain tumors and may be considered a specific cell marker for meningioma.

Similarity: Belongs to the lipocalin family.

Prostaglandin-H2 D-isomerase reacts with human.

OMIM: 176803; gene. [NCBI / EBI]

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