Aim Anthropogenic local weather change is predicted to end in the full loss of glaciers from the excessive mountains of tropical Africa, with profound impacts on the hydrology and ecology of distinctive tropical cold-water lakes positioned downstream from them.
This research examines the biodiversity of Chironomidae (Insecta: Diptera) communities in these scarce Afroalpine lake methods, to be able to decide their uniqueness in relation to lowland African lakes and alpine lakes in temperate areas, and to judge the potential of Afroalpine Chironomidae as organic indicators to observe future modifications in the ecological integrity of their habitat.
Location Mount Kenya (Kenya) and Rwenzori Mountains (Uganda). Methods The species composition of Afroalpine chironomid communities was assessed utilizing latest larval loss of life assemblages extracted from the floor sediments of 11 high-mountain lakes between 2900 and 4575 m. Results have been in contrast with comparable faunal information from 68 East African lakes at low and center elevation (750-2760 m), and with literature information of Chironomidae species distribution in sub-Saharan Africa, the Palaearctic area and elsewhere. All recovered taxa have been absolutely described and illustrated.
Results The 11-lake evaluation yielded 1744 subfossil chironomid larvae belonging to 16 distinct taxa of full-grown larvae, and three taxa of much less differentiated juveniles. Eleven of these 16 are usually not recognized to happen in African lakes at decrease elevation, and eight taxa (or 50% of complete species richness) seem restricted to the particular habitat of chilly lakes above 3900 m, the place night-time freezing is frequent year-round. The faunal transition zone coincides broadly with the Ericaceous zone of terrestrial vegetation (c. 3000-4000 m). Snowline melancholy throughout the Quaternary ice ages should have facilitated dispersion of cold-stenothermous species amongst the excessive mountains of equatorial East Africa, however much less so from or to the Palaearctic area through the Ethiopian highlands.
The microtiter plate provided in this kit has been pre-coated with an antibody specific to Ras Association Domain Containing Protein 1 (RASSF1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated an
Description: A sandwich ELISA kit for detection of Ras Association Domain Containing Protein 1 from Human in samples from blood, serum, plasma, cell culture fluid and other biological fluids.
Gentaur's CCA ELISA kit utilizes the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human CCA. Standards or samples are added to the micro ELISA plate wells and combined with the
Gentaur's CCA ELISA kit utilizes the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Mouse CCA. Standards or samples are added to the micro ELISA plate wells and combined with the
Gentaur's UBC ELISA kit utilizes the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human UBC. Standards or samples are added to the micro ELISA plate wells and combined with the
Description: A sandwich ELISA kit for quantitative measurement of Human UBC (Urinary Bladder Cancer Antigen) in samples from Serum, Plasma, Cell supernatant
ELISA kit for Human CTAG1B (Cancer/Testis Antigen 1B)
The microtiter plate provided in this kit has been pre-coated with an antibody specific to Cancer/Testis Antigen 1B (CTAG1B). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to
Description: A sandwich ELISA kit for detection of Cancer/Testis Antigen 1B from Human in samples from blood, serum, plasma, cell culture fluid and other biological fluids.
Anti-MAGE-1 (Target for Cancer Immunotherapy) Monoclonal Antibody
The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes (E1s), ubiquitin-co
Description: Quantitative sandwich ELISA for measuring Human Urinary bladder cancer antigen (UBC) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Human Urinary bladder cancer antigen (UBC)
The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes (E1s), ubiquitin-co
Description: Quantitative sandwich ELISA for measuring Human Urinary bladder cancer antigen (UBC) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Human Urinary bladder cancer antigen (UBC)
The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes (E1s), ubiquitin-co
Description: Quantitative sandwich ELISA for measuring Human Urinary bladder cancer antigen (UBC) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
MAGE-1 (Target for Cancer Immunotherapy); Clone MA454 (Concentrate)
Description: Quantitative sandwich ELISA for measuring Human Tumor marker DR-70 for lung cancer (DR-70TM) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Human Tumor marker DR-70 for lung cancer (DR-70TM)
Description: Quantitative sandwich ELISA for measuring Human Tumor marker DR-70 for lung cancer (DR-70TM) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Human Tumor marker DR-70 for lung cancer (DR-70TM)
Description: Quantitative sandwich ELISA for measuring Human Tumor marker DR-70 for lung cancer (DR-70TM) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
Gentaur's BRCA2 CLIA kit utilizes the Sandwich- CLIA principle. The micro CLIA plate provided in this kit has been pre-coated with an antibody specific to Human BRCA2 . Standards or samples are added to the micro CLIA plate wells and combined with th
Description: A sandwich CLIA kit for quantitative measurement of Human BRCA2 (Breast Cancer Susceptibility Protein 2) in samples from Serum, Plasma, Cell supernatant
ELISA kit for Human Breast cancer type 1 susceptibility protein
Description: Enzyme-linked immunosorbent assay kit for quantification of Human Breast cancer type 1 susceptibility protein in samples from serum, plasma, tissue homogenates and other biological fluids.
ELISA kit for Human Serologically defined colon cancer antigen 3
Description: Enzyme-linked immunosorbent assay kit for quantification of Human Serologically defined colon cancer antigen 3 in samples from serum, plasma, tissue homogenates and other biological fluids.
Human tumor marker DR- 70 for lung cancer ELISA Kit
The microtiter plate provided in this kit has been pre-coated with an antibody specific to Deleted In Liver Cancer 1 (DLC1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to D
Description: A sandwich ELISA kit for detection of Deleted In Liver Cancer 1 from Human in samples from blood, serum, plasma, cell culture fluid and other biological fluids.
ELISA kit for Human ECRG4 (Esophageal Cancer Related Gene 4)
The microtiter plate provided in this kit has been pre-coated with an antibody specific to Esophageal Cancer Related Gene 4 (ECRG4). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody speci
Description: A sandwich ELISA kit for detection of Esophageal Cancer Related Gene 4 from Human in samples from blood, serum, plasma, cell culture fluid and other biological fluids.
ELISA kit for Human BRCA2 (Breast Cancer Susceptibility Protein 2)
The microtiter plate provided in this kit has been pre-coated with an antibody specific to Breast Cancer Susceptibility Protein 2 (BRCA2). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody
Description: A sandwich ELISA kit for detection of Breast Cancer Susceptibility Protein 2 from Human in samples from blood, serum, plasma, cell culture fluid and other biological fluids.
ELISA kit for Human BRCA1 (Breast Cancer Susceptibility Protein 1)
The microtiter plate provided in this kit has been pre-coated with an antibody specific to Breast Cancer Susceptibility Protein 1 (BRCA1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody
Description: A sandwich ELISA kit for detection of Breast Cancer Susceptibility Protein 1 from Human in samples from blood, serum, plasma, cell culture fluid and other biological fluids.
ELISA kit for Mouse BRCA2 (Breast Cancer Susceptibility Protein 2)
The microtiter plate provided in this kit has been pre-coated with an antibody specific to Breast Cancer Susceptibility Protein 2 (BRCA2). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody
Description: A sandwich ELISA kit for detection of Breast Cancer Susceptibility Protein 2 from Mouse in samples from blood, serum, plasma, cell culture fluid and other biological fluids.
ELISA kit for Mouse Deleted In Liver Cancer 1 (DLC1)
Deleted in Liver Cancer 1 is deleted in the primary tumor of hepatocellular carcinoma. It maps to 8p22-p21.3, a region frequently deleted in solid tumors. It is suggested that this gene is a candidate tumor suppressor gene for human liver cancer, as
Description: Quantitative sandwich ELISA for measuring Mouse Deleted In Liver Cancer 1 (DLC1) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Mouse Deleted In Liver Cancer 1 (DLC1)
Deleted in Liver Cancer 1 is deleted in the primary tumor of hepatocellular carcinoma. It maps to 8p22-p21.3, a region frequently deleted in solid tumors. It is suggested that this gene is a candidate tumor suppressor gene for human liver cancer, as
Description: Quantitative sandwich ELISA for measuring Mouse Deleted In Liver Cancer 1 (DLC1) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Mouse Deleted In Liver Cancer 1 (DLC1)
Deleted in Liver Cancer 1 is deleted in the primary tumor of hepatocellular carcinoma. It maps to 8p22-p21.3, a region frequently deleted in solid tumors. It is suggested that this gene is a candidate tumor suppressor gene for human liver cancer, as
Description: Quantitative sandwich ELISA for measuring Mouse Deleted In Liver Cancer 1 (DLC1) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Human Breast cancer susceptibility protein 1 (BRCA1)
BRCA1 is a human gene, some mutations of which are associated with a significant increase in the risk of breast cancer, as well as other cancers. BRCA1 belongs to a class of genes known as tumor suppressors, which maintains genomic integrity to pre
Description: Quantitative sandwich ELISA for measuring Human Breast cancer susceptibility protein 1 (BRCA1) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Human Breast cancer susceptibility protein 1 (BRCA1)
BRCA1 is a human gene, some mutations of which are associated with a significant increase in the risk of breast cancer, as well as other cancers. BRCA1 belongs to a class of genes known as tumor suppressors, which maintains genomic integrity to pre
Description: Quantitative sandwich ELISA for measuring Human Breast cancer susceptibility protein 1 (BRCA1) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Human Breast cancer susceptibility protein 1 (BRCA1)
BRCA1 is a human gene, some mutations of which are associated with a significant increase in the risk of breast cancer, as well as other cancers. BRCA1 belongs to a class of genes known as tumor suppressors, which maintains genomic integrity to pre
Description: Quantitative sandwich ELISA for measuring Human Breast cancer susceptibility protein 1 (BRCA1) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Human Deleted In Liver Cancer 1 (DLC1)
Deleted in Liver Cancer 1 is deleted in the primary tumor of hepatocellular carcinoma. It maps to 8p22-p21.3, a region frequently deleted in solid tumors. It is suggested that this gene is a candidate tumor suppressor gene for human liver cancer, as
Description: Quantitative sandwich ELISA for measuring Human Deleted In Liver Cancer 1 (DLC1) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Human Deleted In Liver Cancer 1 (DLC1)
Deleted in Liver Cancer 1 is deleted in the primary tumor of hepatocellular carcinoma. It maps to 8p22-p21.3, a region frequently deleted in solid tumors. It is suggested that this gene is a candidate tumor suppressor gene for human liver cancer, as
Description: Quantitative sandwich ELISA for measuring Human Deleted In Liver Cancer 1 (DLC1) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Human Deleted In Liver Cancer 1 (DLC1)
Deleted in Liver Cancer 1 is deleted in the primary tumor of hepatocellular carcinoma. It maps to 8p22-p21.3, a region frequently deleted in solid tumors. It is suggested that this gene is a candidate tumor suppressor gene for human liver cancer, as
Description: Quantitative sandwich ELISA for measuring Human Deleted In Liver Cancer 1 (DLC1) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Rat Deleted In Liver Cancer 1 (DLC1)
Deleted in Liver Cancer 1 is deleted in the primary tumor of hepatocellular carcinoma. It maps to 8p22-p21.3, a region frequently deleted in solid tumors. It is suggested that this gene is a candidate tumor suppressor gene for human liver cancer, as
Description: Quantitative sandwich ELISA for measuring Rat Deleted In Liver Cancer 1 (DLC1) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Rat Deleted In Liver Cancer 1 (DLC1)
Deleted in Liver Cancer 1 is deleted in the primary tumor of hepatocellular carcinoma. It maps to 8p22-p21.3, a region frequently deleted in solid tumors. It is suggested that this gene is a candidate tumor suppressor gene for human liver cancer, as
Description: Quantitative sandwich ELISA for measuring Rat Deleted In Liver Cancer 1 (DLC1) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Rat Deleted In Liver Cancer 1 (DLC1)
Deleted in Liver Cancer 1 is deleted in the primary tumor of hepatocellular carcinoma. It maps to 8p22-p21.3, a region frequently deleted in solid tumors. It is suggested that this gene is a candidate tumor suppressor gene for human liver cancer, as
Description: Quantitative sandwich ELISA for measuring Rat Deleted In Liver Cancer 1 (DLC1) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Canine Deleted In Liver Cancer 1 (DLC1)
Deleted in Liver Cancer 1 is deleted in the primary tumor of hepatocellular carcinoma. It maps to 8p22-p21.3, a region frequently deleted in solid tumors. It is suggested that this gene is a candidate tumor suppressor gene for human liver cancer, as
Description: Quantitative sandwich ELISA for measuring Canine Deleted In Liver Cancer 1 (DLC1) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Canine Deleted In Liver Cancer 1 (DLC1)
Deleted in Liver Cancer 1 is deleted in the primary tumor of hepatocellular carcinoma. It maps to 8p22-p21.3, a region frequently deleted in solid tumors. It is suggested that this gene is a candidate tumor suppressor gene for human liver cancer, as
Description: Quantitative sandwich ELISA for measuring Canine Deleted In Liver Cancer 1 (DLC1) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Canine Deleted In Liver Cancer 1 (DLC1)
Deleted in Liver Cancer 1 is deleted in the primary tumor of hepatocellular carcinoma. It maps to 8p22-p21.3, a region frequently deleted in solid tumors. It is suggested that this gene is a candidate tumor suppressor gene for human liver cancer, as
Description: Quantitative sandwich ELISA for measuring Canine Deleted In Liver Cancer 1 (DLC1) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
Monoclonal MAGE-1 (Target for Cancer Immunotherapy) Antibody, Clone: MA454
Description: A Monoclonal antibody against Human MAGE-1 (Target for Cancer Immunotherapy). The antibodies are raised in Mouse and are from clone MA454. This antibody is applicable in IHC, IF, FC
Monoclonal MAGE-1 (Target for Cancer Immunotherapy) Antibody, Clone: SPM282
Description: A Monoclonal antibody against Human MAGE-1 (Target for Cancer Immunotherapy). The antibodies are raised in Mouse and are from clone SPM282. This antibody is applicable in IHC, IF, FC
MAGE-1 (Target for Cancer Immunotherapy); Clone MZ2E/838 (Concentrate)
Gentaur's CCSA-2 ELISA kit utilizes the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human CCSA-2. Standards or samples are added to the micro ELISA plate wells and combined wit
Description: A sandwich ELISA kit for quantitative measurement of Human CCSA-2 (Colon Cancer Specific Antigen-2) in samples from Serum, Plasma, Cell supernatant
Main conclusions Chironomid communities in glacier-fed lakes on Africa’s highest mountains are extremely distinct from these of lowland African lakes, and probably distinctive on a continental scale. By advantage of wonderful preservation and their spatial and temporal integration of local people dynamics, chironomid larval loss of life assemblages extracted from floor sediments are highly effective organic indicators for monitoring the hydrological and ecological modifications related to the present retreat and loss of Africa’s glaciers.
ORIGINAL ARTICLE: Taxonomy and diversity of Afroalpine Chironomidae (Insecta: Diptera) on Mount Kenya and the Rwenzori Mountains, East Africa.
Revision of the genus Deltaspis Audinet-Serville, 1834 with systematic evaluation and new taxa of Trachyderini with emarginate-truncate mandibles (Insecta: Coleoptera: Cerambycidae).
The genera Deltaspis Audinet-Serville, 1834 and Muscidora, Thomson, 1864 (Coleoptera: Cerambycidae: Cerambycinae: Trachyderini) are revised.
Two new genera Neoxoplus gen. nov. and Deltaspiopsis gen. nov., are described. Two species beforehand included in Deltaspis [D. cruentus, (LeConte, 1862), and D. ivae Beierl Barchet-Beierl, 1999] are transferred to the new genus Neoxoplus with N. cruentus designated as the sort species. Four different Deltaspis species [D. alutacea Bates, 1885, D. marginella Bates, 1891, D. nigripennis Bates, 1880, and D. tumacacorii (Knull, 1944)] are transferred to Muscidora Thomson, 1864. Two species [D. disparilis Bates, 1891, and D. variabilis Bates, 1891] are transferred to the new genus Deltaspiopsis with D. disparilis designated as sort species, and the remaining species [D. moesta Bates, 1885, D. rubens Bates, 1885, and D. subopaca Chemsak Linsley, 1982] are transferred to Crossidius LeConte, 1851. Keys to intently associated genera, above talked about genera and species together with illustrations of the out there species in shade are included.
New species described embrace: Muscidora bezarki sp. nov. from south-central Mexico (Puebla, Oaxaca); Muscidora coriacea sp. nov. from southeastern Mexico (Oaxaca and Chiapas); Muscidora nigrescens clinei subsp. nov. (Jalisco); and Muscidora similis sp. nov. from western Mexico (Sinaloa and Sonora).
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