fast limb muscle, high activity of isoenzyme CA3, message levels of isoenzyme CA2 and CA4 are higher in extraocular muscle than in extensor digitorum longus, expression of isoenzyme CA5 is equivalent in extraocular muscle and extensor digitorum longus
isoenzyme CA3 is depressed, message levels of isoenzyme CA2 and CA4 are higher in extraocular muscle than in extensor digitorum longus, expression of isoenzyme CA5 is equivalent in extraocular muscle and extensor digitorum longus
elevated levels of extracellular carbonic anhydrase-I (CA-I) in vitreous from individuals with diabetic retinopathy, suggesting that retinal hemorrhage and erythrocyte lysis contribute to the diabetic vitreous proteome
Pl-can temporal and spatial expression profiles, analyzed throughout embryo development by comparative quantitative PCR and whole-mount in situ hybridization (WMISH), shows that Pl-can mRNA is specifically expressed in the primary mesenchyme cells of the embryo and levels increase along with the growth of the embryonic skeleton, reaching a peak at the pluteus stage
at apical membrane of some epithelial cells surrounding the tertiary water channels and to a lesser extent at the apical membrane of some epithelial apical immunofluorescence epithelial cells as compared with the control
carbonic anhydrase activity is sensitive to zinc and copper inputs from the environment. Carbonic anhydrase activity is increased by zinc or iron in the range of lower Zn or Fe additions, and is inhibited by zinc or iron for the higher Zn or Fe additions. Carbonic anhydrase activity is inhibited by copper at a very low Cu addition level
carbonic anhydrase H differs from carbonic anhydrase C in having an Asp rather than Asn at a position 9 residues removed from the COOH-terminal end of the molecule
erythrocyte isoform CA XIII. About 90% of the CA activity in erythrocytes is due to a high activity CA II-like isoform, 10% are due to the low activity CA XIII isozyme
expression of the cytoplasmic isoform in the posterior gill (CasCAc) undergoes a significantly greater degree of up-regulation after exposure to low salinity (15·p.p.t.) as compared to high salinity. CasCAc has the largest scope of induction (100fold) reported for any transportrelated protein in the gill
the membrane associated isoform CasCAg is present in much higher levels of mRNA expression in both anterior and posterior gills in crabs acclimated to high salinity (35·p.p.t.) compared to crabs acclimated to low salinity
carbonic anhydrase activity is low and uniform across gills in shrimp acclimated to osmolarity of 30 ppt, but carbonic anhydrase activity increases in all gils after exposure to both low and high salinities. Anterior gills have the largest increases in carbonic anhydrase activity, and levels of increase are approximately the same for low and high salinity exposure. Induction of branchial carbonic anhydrase appears to be functionally important in both hyper- and hypo-osmotic regulations of hemolymph osmotic concentrations
pavement cells forming the gill epithelial surface layer, mucous cells, pillar cells bordering the vascular channels of the secondary lamellae, chloride cells, mitochondria-rich cells located in the primary epithelium, interlamellar regions, bases of the secondary lamellae
in both renal cortex and medulla the strongest expression is confined to the collecting ducts and weak expression can be found in the glomerulus, carbonic anhydrase XIII
strongest expression of CA XIV is detected in the cortex region, where it is restricted to the proximal tubules of S1 and S2 segments, carbonic anhydrase XIV
carbonic anhydrase 3. CA3 gene transcripts are the most abundant CA transcripts in the leaf tissues of all plants examined, being at least 50 times more plentiful than either CA1 or CA2 mRNAs. CA3 gene expression is at least 1000 times greater in leaves than in roots or flowers
low transcript level, carbonic anhydrase 1. Levels of CA1 mRNA are highest in leaves, albeit about 100fold lower than the levels of CA3 transcripts in these organs
low transcript level, carbonic anhydrase 1. Levels of CA1 mRNA are highest in leaves, albeit about 100fold lower than the levels of CA3 transcripts in these organs
carbonic anhydrase 3. CA3 gene transcripts are the most abundant CA transcripts in the leaf tissues of all plants examined, being at least 50 times more plentiful than either CA1 or CA2 mRNAs. CA3 gene expression is at least 1000 times greater in leaves than in roots or flowers
expression in the posterior mantle pallial (pMP) is significantly higher than that in the anterior mantle pallial (aMP), and expression is low in the mantle center (MC). Expression in the aMP, pMP and MC is significantly higher in purple mussels compared with that in white mussels
the effect of zinc on the activity of CAIX in MDA-MB-231 breast cancer cells and membrane ghosts derived from these cells is examined. In neither setting any significant elevation of CAIX activity is measured
slow-fibre type and fast-fibre type. Slow-fibre type muscle contains carbonic anhydrase I, II and III. Fast-fibre type muscle contains carbonic anhydrase I and II
inner cortical cells, both genes encoding LjCAA1 and LjCAA2 code for nodule enhanced carbonic anhydrase isoforms, which are induced early during nodule development, overview
inner cortical cells, both genes encoding LjCAA1 and LjCAA2 code for nodule enhanced carbonic anhydrase isoforms, which are induced early during nodule development, overview
tibial anterior musle and soleus muscle, broad expression of CAIII in mouse skeletal muscles. Postnatal downregulation and reexpression of CAIII in adult tibial anterior muscle
tibial anterior musle and soleus muscle, broad expression of CAIII in mouse skeletal muscles. Postnatal downregulation and reexpression of CAIII in adult tibial anterior muscle
immunohistochemic analysis of enzyme distribution in zebrafish tissues, quantitative expression analysis of ca6 mRNA in wild-type and the ca6 morphant zebrafish at different stages of development
immunohistochemic analysis of enzyme distribution in zebrafish tissues, quantitative expression analysis of ca6 mRNA in wild-type and the ca6 morphant zebrafish at different stages of development
CA XIV is highly expressed in all parts of the central nervous system and to a lesser extent in adult liver, heart, small intestine, colon, kidney, urinary bladder and skeletal muscle
CA XIV is highly expressed in all parts of the central nervous system and to a lesser extent in adult liver, heart, small intestine, colon, kidney, urinary bladder and skeletal muscle
the protein sequence of the enzyme contains a signal peptide composed of 19 amino acid residues (MVVATVILLLACAAVSNCV). Quantitative RT-PCR expression analysis and in-situ hybridization in mussel tissues, overview
the protein sequence of the enzyme contains a signal peptide composed of 19 amino acid residues (MVVATVILLLACAAVSNCV). Quantitative RT-PCR expression analysis and in-situ hybridization in mussel tissues, overview
expression patterns of isozymes LjCAA1 and LjCAA2 by in situ hybridization, both are expressed in nodule inner cortical cells, vascular bundles and central tissue, overview
expression patterns of isozymes LjCAA1 and LjCAA2 by in situ hybridization, both are expressed in nodule inner cortical cells, vascular bundles and central tissue, overview
expression patterns of isozymes LjCAA1 and LjCAA2 by in situ hybridization, both are expressed in nodule inner cortical cells, vascular bundles and central tissue, overview
expression patterns of isozymes LjCAA1 and LjCAA2 by in situ hybridization, both are expressed in nodule inner cortical cells, vascular bundles and central tissue, overview
immunohistochemic analysis using monoclonal antibody against CP3, mAb CP3, detailed overview. No CAIII is detected by CP3 in mouse heart and bladder smooth muscle, or in extensor digitorum longus muscle
immunohistochemic analysis using monoclonal antibody against CP3, mAb CP3, detailed overview. No CAIII is detected by CP3 in mouse heart and bladder smooth muscle, or in extensor digitorum longus muscle
immunohistochemic analysis using monoclonal antibody against CP3, mAb CP3, detailed overview. No CAIII is detected by CP3 in mouse heart and bladder smooth muscle, or in extensor digitorum longus muscle
the DDCA is localized apically in certain epithelial cells near the base of the ctenidial filament and the epithelial cells surrounding the tertiary water channels. No or very poor expression in inner mantle, foot muscle, byssal muscle, heart, hepatopancreas, and kidney of Tridacna squamosa kept in darkness for 12 h, immunofluorescent tissue distribution analysis
the DDCA is localized apically in certain epithelial cells near the base of the ctenidial filament and the epithelial cells surrounding the tertiary water channels. No or very poor expression in inner mantle, foot muscle, byssal muscle, heart, hepatopancreas, and kidney of Tridacna squamosa kept in darkness for 12 h, immunofluorescent tissue distribution analysis
the outer mantle, which contains the highest density of tertiary tubules and exosymbiont zooxanthellae, displays high level of CA2-like expression, and CA2-like is localized to the tubule epithelial cells. Cloning of CA2 homolog (CA2-like) from the fleshy and colorful outer mantle as well as the thin and whitish inner mantle of Tridacna squamosa to determine its cellular and subcellular localization. Immunofluorescent enzyme localization study