The area from New Guinea via Oceania sustains the world’s most numerous set of columbids. We describe osteological characters of the hindlimb (femur, tibiotarsus, tarsometatarsus) that divide the Papuan-Oceanic pigeons and doves into three teams based mostly on practical morphology: “arboreal” (Hemiphaga, Ducula, Ptilinopus, Drepanoptila, Gymnophaps), “intermediate” (Columba, Macropygia, Reinwardtoena), and “terrestrial” (Gallicolumba [includes Alopecoenas], Trugon, Microgoura, Goura, Chalcophaps, Geopelia, Henicophaps, Caloenas, Didunculus, Otidiphaps).
The arboreal and terrestrial teams are every distinctive osteologically, particularly within the tibiotarsus and tarsometatarsus, that are brief relative to the femur within the arboreal group, and lengthy relative to the femur within the terrestrial group. The intermediate pigeons are extra just like arboreal than to terrestrial pigeons, however nonetheless slot in neither group. To estimate the phylogenetic relationships amongst or inside these three teams is considerably tentative utilizing hindlimb osteology alone, though all 5 genera of arboreal pigeons have unbiased molecular proof of relatedness, as do a lot of the genera of terrestrial pigeons. Utilizing the hindlimb and different osteological information as a framework, we describe a brand new extinct genus and species of pigeon, Tongoenas burleyi, from Holocene archaeological and Pleistocene paleontological websites on six islands (Foa, Lifuka, `Uiha, Ha`afeva, Tongatapu, and `Eua) within the Kingdom of Tonga.
Tongoenas was a large-sized member of the “arboreal” pigeon group, with osteological characters that relate it to Ducula, Gymnophaps, and Hemiphaga (usually cover frugivores) quite than with the “terrestrial” pigeons (extra ground-dwelling and granivorous) similar to Gallicolumba, Trugon, Microgoura, Goura, and so forth. (others listed above). Amongst volant columbids, residing or extinct, solely the species of Goura (from New Guinea) are bigger than Tongoenas. From a lot of the similar prehistoric websites, we additionally report new materials of the practically as massive, extinct pigeon Ducula shutleri Worthy Burley, not too long ago described from islands within the Vava`u Group of Tonga. Thus, D. shutleri additionally was widespread in Tonga earlier than human influence. The prehistoric anthropogenic loss in Tonga of Tongoenas burleyi, Ducula shutleri, and different columbids undoubtedly had a detrimental influence on the dispersal regimes of Tongan forest bushes. At first human contact about 2850 years in the past, no less than 9 species of columbids in six genera inhabited the Tongan islands, the place solely 4 species in three genera exist in the present day.
Biogeographic problem-solving reveals the Late Pleistocene translocation of a short-faced bear to the California Channel Islands
An correct understanding of biodiversity of the previous is crucial for contextualizing biodiversity patterns and developments within the current. Rising methods are refining our potential to decipher in any other case cryptic human-mediated species translocations throughout the Quaternary, but these methods are sometimes utilized in isolation, quite than a part of an interdisciplinary hypothesis-testing toolkit, limiting their scope and utility. Right here we illustrate using such an integrative method and report the incidence of North America’s largest terrestrial mammalian carnivore, the short-faced bear, Arctodus simus, from Daisy Cave (CA-SMI-261), an vital early human occupation web site on the California Channel Islands.
We recognized the specimen by corroborating morphological, protein, and mitogenomic traces of proof, and evaluated the potential pure and anthropogenic mechanisms of its transport and deposition. Whereas representing only a single specimen, our mixture of methods opened a window into the habits of an enigmatic species, suggesting that A. simus was a wide-ranging scavenger using terrestrial and marine carcasses. This discovery highlights the utility of bridging archaeological and paleontological datasets to disentangle advanced biogeographic situations and reveal sudden biodiversity for island methods worldwide.
A new genus and species of pigeon (Aves, Columbidae) from the Kingdom of Tonga, with an evaluation of hindlimb osteology of columbids from Oceania
A Whole-Proof Dated Phylogeny of Echinoidea Combining Phylogenomic and Paleontological Information
Phylogenomic and paleontological information represent complementary assets for unravelling the phylogenetic relationships and divergence occasions of lineages, but few research have tried to totally combine them. A number of distinctive properties of echinoids (sea urchins) make them particularly helpful for such synthetizing approaches, together with a exceptional fossil report that may be integrated into specific phylogenetic hypotheses. We revisit the phylogeny of crown group Echinoidea utilizing a total-evidence relationship method that mixes the biggest phylogenomic dataset for the clade, a large-scale morphological matrix with a dense fossil sampling, and a novel compendium of tip and node age constraints.
Rat alpha 2-Macroglobulin (A2M) ELISA kit 96 tests, Quantitative
Should the Human Alpha-2-Macroglobulin (a2M) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A sandwich quantitative ELISA assay kit for detection of Human Alpha-2-Macroglobulin (a2M) in samples from serum, plasma, urine or other biological fluids.
Should the Human Alpha-2-Macroglobulin (a2M) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A sandwich quantitative ELISA assay kit for detection of Human Alpha-2-Macroglobulin (a2M) in samples from serum, plasma, urine or other biological fluids.
Should the Mouse Alpha-2-Macroglobulin (a2M) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A sandwich quantitative ELISA assay kit for detection of Mouse Alpha-2-Macroglobulin (a2M) in samples from serum, plasma, urine or other biological fluids.
Should the Mouse Alpha-2-Macroglobulin (a2M) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A sandwich quantitative ELISA assay kit for detection of Mouse Alpha-2-Macroglobulin (a2M) in samples from serum, plasma, urine or other biological fluids.
Should the Rat Alpha-2-Macroglobulin (a2M) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A sandwich quantitative ELISA assay kit for detection of Rat Alpha-2-Macroglobulin (a2M) in samples from serum, plasma, urine or other biological fluids.
Should the Rat Alpha-2-Macroglobulin (a2M) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A sandwich quantitative ELISA assay kit for detection of Rat Alpha-2-Macroglobulin (a2M) in samples from serum, plasma, urine or other biological fluids.
Description: A polyclonal antibody against A2M. Recognizes A2M from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC
Buffer: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Description: A polyclonal antibody against A2M. Recognizes A2M from Human. This antibody is Unconjugated. Tested in the following application: WB, ELISA;WB:1/500-1/2000.ELISA:1/20000
Buffer: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Description: A polyclonal antibody against A2M. Recognizes A2M from Human. This antibody is Unconjugated. Tested in the following application: IHC, ELISA;IHC:1/100-1/300.ELISA:1/40000
Buffer: Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 >95%, Protein G purified
Description: A polyclonal antibody against A2M. Recognizes A2M from Human. This antibody is Unconjugated. Tested in the following application: ELISA, IHC, IF; Recommended dilution: IHC:1:20-1:200, IF:1:50-1:200
Description: Alpha-2-macroglobulin is a protease inhibitor and cytokine transporter. It inhibits many proteases, including trypsin, thrombin and collagenase. A2M is implicated in Alzheimer disease (AD) due to its ability to mediate the clearance and degradation of A-beta, the major component of beta-amyloid deposits.
Buffer: Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 >95%, Protein G purified
Description: A polyclonal antibody against A2M. Recognizes A2M from Human. This antibody is FITC conjugated. Tested in the following application: ELISA
Buffer: Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 >95%, Protein G purified
Description: A polyclonal antibody against A2M. Recognizes A2M from Human. This antibody is Biotin conjugated. Tested in the following application: ELISA
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human A2M (N-term). This antibody is tested and proven to work in the following applications:
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human A2M (C-term). This antibody is tested and proven to work in the following applications:
Description: Description of target: The protein encoded by this gene is a protease inhibitor and cytokine transporter. It uses a bait-and-trap mechanism to inhibit a broad spectrum of proteases, including trypsin, thrombin and collagenase. It can also inhibit inflammatory cytokines, and it thus disrupts inflammatory cascades. Mutations in this gene are a cause of alpha-2-macroglobulin deficiency. This gene is implicated in Alzheimer's disease (AD) due to its ability to mediate the clearance and degradation of A-beta, the major component of beta-amyloid deposits. A related pseudogene, which is also located on the p arm of chromosome 12, has been identified.;Species reactivity: Human;Application: ELISA;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 19.2 pg/mL
Description: Description of target: The protein encoded by this gene is a protease inhibitor and cytokine transporter. It uses a bait-and-trap mechanism to inhibit a broad spectrum of proteases, including trypsin, thrombin and collagenase. It can also inhibit inflammatory cytokines, and it thus disrupts inflammatory cascades. Mutations in this gene are a cause of alpha-2-macroglobulin deficiency. This gene is implicated in Alzheimer's disease (AD) due to its ability to mediate the clearance and degradation of A-beta, the major component of beta-amyloid deposits. A related pseudogene, which is also located on the p arm of chromosome 12, has been identified.;Species reactivity: Human;Application: ELISA;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 0.35 ng/mL
Description: Description of target: plays a role in acute phase response; activated form induces a decrease in N-methyl-D-aspartate (NMDA) mediated calcium signaling [RGD, Feb 2006];Species reactivity: Rat;Application: ELISA;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 5.9 ng/mL
Description: Description of target: plays a role in acute phase response; activated form induces a decrease in N-methyl-D-aspartate (NMDA) mediated calcium signaling.;Species reactivity: Rat;Application: ELISA;Assay info: ;Sensitivity: < 5.9ng/mL
Description: Description of target: Is able to inhibit all four classes of proteinases by a unique 'trapping' mechanism. This protein has a peptide stretch, called the 'bait region' which contains specific cleavage sites for different proteinases. When a proteinase cleaves the bait region, a conformational change is induced in the protein which traps the proteinase. The entrapped enzyme remains active against low molecular weight substrates (activity against high molecular weight substrates is greatly reduced). Following cleavage in the bait region a thioester bond is hydrolyzed and mediates the covalent binding of the protein to the proteinase.;Species reactivity: Rat;Application: ;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 4.02 ng/mL
Description: Description of target: Is able to inhibit all four classes of proteinases by a unique 'trapping' mechanism. This protein has a peptide stretch, called the 'bait region' which contains specific cleavage sites for different proteinases. When a proteinase cleaves the bait region, a conformational change is induced in the protein which traps the proteinase. The entrapped enzyme remains active against low molecular weight substrates (activity against high molecular weight substrates is greatly reduced). Following cleavage in the bait region a thioester bond is hydrolyzed and mediates the covalent binding of the protein to the proteinase.;Species reactivity: Bovine;Application: ;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 1.47 ng/mL
Description: Description of target: Alpha-2-macroglobulin, also known as A2M or CPAMD5 is a large plasma protein found in the blood. This gene is mapped to 12p13.31. Alpha-2-macroglobulin is a protease inhibitor and cytokine transporter. It inhibits many proteases, including trypsin, thrombin and collagenase. A2M is implicated in Alzheimer disease(AD) due to its ability to mediate the clearance and degradation of A-beta, the major component of beta-amyloid deposits. This gene is able to inhibit all four classes of proteinases by a unique 'trapping' mechanism. This protein has a peptide stretch, called the 'bait region' which contains specific cleavage sites for different proteinases. When a proteinase cleaves the bait region, a conformational change is induced in the protein which traps the proteinase. The entrapped enzyme remains active against low molecular weight substrates(activity against high molecular weight substrates is greatly reduced). Following cleavage in the bait region a thioester bond is hydrolyzed and mediates the covalent binding of the protein to the proteinase.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: <20pg/ml
Description: Description of target: The protein encoded by this gene is a protease inhibitor and cytokine transporter. It uses a bait-and-trap mechanism to inhibit a broad spectrum of proteases, including trypsin, thrombin and collagenase. It can also inhibit inflammatory cytokines, and it thus disrupts inflammatory cascades. Mutations in this gene are a cause of alpha-2-macroglobulin deficiency. This gene is implicated in Alzheimer's disease (AD) due to its ability to mediate the clearance and degradation of A-beta, the major component of beta-amyloid deposits. A related pseudogene, which is also located on the p arm of chromosome 12, has been identified.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: < 1.6 ng/ml
Description: A polyclonal antibody raised in Goat that recognizes and binds to Human A2M / Alpha-2-Macroglobulin . This antibody is tested and proven to work in the following applications:
Description: A polyclonal antibody raised in Goat that recognizes and binds to Human A2M / Alpha-2-Macroglobulin . This antibody is tested and proven to work in the following applications:
To this finish, we develop a novel technique for subsampling phylogenomic datasets that selects loci with excessive phylogenetic sign, low systematic biases and enhanced clock-like habits. Our outcomes reveal that combining totally different information sources will increase topological accuracy and helps resolve conflicts between molecular and morphological information. Notably, we current a brand new speculation for the origin of sand {dollars}, and restructure the relationships between stem and crown echinoids in a means that means a protracted stretch of undiscovered evolutionary historical past of the crown group within the late Paleozoic. Our efforts assist bridge the hole between phylogenomics and phylogenetic paleontology, offering a mannequin instance of the advantages of mixing the 2.
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