Impacts of climate change on current and future invasion of Prosopis juliflora in Ethiopia: environmental and socio-economic implications
Prosopis juliflora is a serious attacker, causing ecological and economic damage that large in Ethiopia. Thus, it is important to examine the potential of P. juliflora invasion dynamics at national level under climate change scenarios affect a better decision making process in the management of this invasive species.
We derived a consensus model of five models to examine current approaches and future (2050 and 2070) climatic suitability for P. juliflora under two climate scenarios (RCP4.5 and RCP8.5) in Ethiopia. Under the current climate scenario, 94.8% from non-suitable for the formation of P. juliflora and invasion while 0.4% (4.56 million ha) was very suitable.
In 2050, the area that is suitable for P. juliflora is expected to increase by 55.6% and 63.6%, while the area is quite appropriate projected to increase by 33.3% and 42.9% under RCP4.5 and climate RCP8 .5 scenarios, respectively. Compared to the current climate conditions, in 2070, the area very suitable for the species are projected to increase 73.3% (3.43 million ha) and 80.0% (3.65 million ha) under RCP4.5 and RCP8.5 scenarios, respectively. By closing the current, invasive species have already caused a significant impact on rangelands in many parts of the country.
Further expansion will exacerbate the problem, which caused damage to the environment and a booming economy, thus threatening the people’s livelihood. negative economic and environmental impact caused by the species will be high if the measures of prevention and effective management is not taken seriously, and it became one of the main challenges for the 21st century pastoralism and their livelihood. We recommend a national effort to combat organized P. juliflora expansion into new areas, especially in regions and protected areas is estimated as the limit of expansion potential.
Impacts of climate change on current and future invasion of Prosopis juliflora in Ethiopia: environmental and socio-economic implications
Representing and coordinating knowledge ethnobiological
Indigenous peoples have a very big rich and articulated natural sciences. The main objective of the research and ethnobiology anthropology and ecology, conservation biology, and the study of the development is to find ways to integrate this knowledge produced by the scientific community and other academic instituted.
Here I present a challenge to this integration project. I would argue, with reference to the study of psychology and cross-cultural ethnography, that the world model developed in a particular academic discipline does not map to what is in traditional beliefs and practices to cope with nature. traditional ecological knowledge distributed across heterogeneous arrays overlap in indigenous cultural practices, including spiritual practices and rituals that call categories, properties, and clear causal model that is not in general converge with those of academic sciences. In light of this divergence, I argue that we should abandon the integration project, and concludes by sketching the idea of coordination of knowledge as a possible successor framework.
seasonal variations in the diversity of seaweeds studied in Olaikuda and Vadakkadu, two coastal areas unexplored in Rameshwaram island on the southern coast of India. A comprehensive survey on seasonal changes in diversity of seaweed made the study and the data were analyzed for the different diversity index. In each location, three transects 100 m gap is taken and in each transect 10 square, a total of 30 squares drawn to the diversity of seaweed.
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 RAB11FIP3. Recognizes RAB11FIP3 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: IHC, ELISA;IHC:1/100-1/300.ELISA:1/10000
Buffer: Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific
Description: A polyclonal antibody against RAB11FIP3. Recognizes RAB11FIP3 from Human, Mouse. This antibody is Unconjugated. Tested in the following application: ELISA, IHC;IHC:1:50-1:100
Buffer: Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific
Description: A polyclonal antibody against RAB11FIP3. Recognizes RAB11FIP3 from Human, Mouse. This antibody is Unconjugated. Tested in the following application: ELISA, IHC;IHC:1:50-1:100
Description: Quantitative sandwich ELISA for measuring Human Rab11 family-interacting protein 3 (RAB11FIP3) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Human Rab11 family-interacting protein 3 (RAB11FIP3)
Description: Quantitative sandwich ELISA for measuring Human Rab11 family-interacting protein 3 (RAB11FIP3) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Human Rab11 family-interacting protein 3 (RAB11FIP3)
Description: Quantitative sandwich ELISA for measuring Human Rab11 family-interacting protein 3 (RAB11FIP3) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
Rab11fip3 sgRNA CRISPR/Cas9 All-in-One Lentivector set (Mouse)
Description: This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis. One version of pediatric acute myeloid leukemia is the result of a reciprocal translocation between chromosomes 11 and X, with the breakpoint associated with the genes encoding the mixed-lineage leukemia and septin 2 proteins. This gene encodes four transcript variants encoding three distinct isoforms. An additional transcript variant has been identified, but its biological validity has not been determined.
Description: This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is highly expressed in brain and heart. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. One of the isoforms (known as ARTS) is distinct; it is localized to the mitochondria, and has a role in apoptosis and cancer.
Description: This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB; platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced.
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Description: This gene encodes a protein that is highly similar to the CDC10 protein of Saccharomyces cerevisiae. The protein also shares similarity with Diff 6 of Drosophila and with H5 of mouse. Each of these similar proteins, including the yeast CDC10, contains a GTP-binding motif. The yeast CDC10 protein is a structural component of the 10 nm filament which lies inside the cytoplasmic membrane and is essential for cytokinesis. This human protein functions in gliomagenesis and in the suppression of glioma cell growth, and it is required for the association of centromere-associated protein E with the kinetochore. Alternative splicing results in multiple transcript variants. Several related pseudogenes have been identified on chromosomes 5, 7, 9, 10, 11, 14, 17 and 19.
Description: This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB; platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced.
Description: This gene encodes a protein that is highly similar to the CDC10 protein of Saccharomyces cerevisiae. The protein also shares similarity with Diff 6 of Drosophila and with H5 of mouse. Each of these similar proteins, including the yeast CDC10, contains a GTP-binding motif. The yeast CDC10 protein is a structural component of the 10 nm filament which lies inside the cytoplasmic membrane and is essential for cytokinesis. This human protein functions in gliomagenesis and in the suppression of glioma cell growth, and it is required for the association of centromere-associated protein E with the kinetochore. Alternative splicing results in multiple transcript variants. Several related pseudogenes have been identified on chromosomes 5, 7, 9, 10, 11, 14, 17 and 19.
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Description: This gene encodes a guanine-nucleotide binding protein and member of the septin family of cytoskeletal GTPases. Septins play important roles in cytokinesis, exocytosis, embryonic development, and membrane dynamics. Multiple transcript variants encoding different isoforms have been found for this gene.
Description: This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis and the maintenance of cellular morphology. This gene encodes a protein that can form homo- and heterooligomeric filaments, and may contribute to the formation of neurofibrillary tangles in Alzheimer's disease. Alternatively spliced transcript variants have been found but the full-length nature of these variants has not been determined. [provided by RefSeq, Dec 2012]
The Intra-assay Precision is determined when 3 samples with low, middle and high level of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) were tested on 3 different plates, 8 replicates in each plate
Description: This is Competitive Enzyme-linked immunosorbent assay for Antibody Detection.detection of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) in serum, plasma and other biological fluids.
Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) ELISA Kit
The Intra-assay Precision is determined when 3 samples with low, middle and high level of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) were tested on 3 different plates, 8 replicates in each plate
Description: This is Competitive Enzyme-linked immunosorbent assay for Antibody Detection.detection of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) in serum, plasma and other biological fluids.
Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) ELISA Kit
The Intra-assay Precision is determined when 3 samples with low, middle and high level of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) were tested on 3 different plates, 8 replicates in each plate
Description: This is Competitive Enzyme-linked immunosorbent assay for Antibody Detection.detection of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) in serum, plasma and other biological fluids.
Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) ELISA Kit
The Intra-assay Precision is determined when 3 samples with low, middle and high level of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) were tested on 3 different plates, 8 replicates in each plate
Description: This is Competitive Enzyme-linked immunosorbent assay for Antibody Detection.detection of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) in serum, plasma and other biological fluids.
Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) ELISA Kit
Known also as Anti-Sperm Antibody elisa. Alternative names of the recognized antigen: Anti-Spermatozoa Antibodies
Sperm Antibodies
Antisperm Antibodies
Description: Enzyme-linked immunosorbent assay based on the Competitive Inhibition method for detection of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) in samples from serum, plasma and other biological fluids with no significant corss-reactivity with analogues from other species.
ELISA kit for Human Anti-AsAb (Anti-Anti-Sperm Antibody Antibody)
The microtiter plate provided in this kit has been pre-coated with an antigen. Standards or samples are then added to the appropriate microtiter plate wells with a Horseradish Peroxidase (HRP)-conjugated secondary antibody. After TMB substrate soluti
Description: A competitive Inhibition ELISA kit for detection of Anti-Anti-Sperm Antibody Antibody from Human in samples from blood, serum, plasma, cell culture fluid and other biological fluids.
Biodiversity data were analyzed by statistical methods such as graphical and statistical analysis of K-dominance curves with PRIMER software package, cluster analysis, multivariate methods, anosim and diversity indices such as Shannon Weaver diversity index
 Antibody)
 Antibody)
 (pORF))
 (pORF))
)
)
 (Target 1))
 (Target 2))
 (Target 3))
 (Target 1))
 (Target 2))
 (Target 3))
 (pPB-C-His))
 (pPB-N-His))
 (pPM-C-HA))
 (pPM-C-His))
 (pPB-C-His))
 (pPB-N-His))
 (pPM-C-HA))
 (pPM-C-His))
 ELISA Kit)
ELISA Kit)
)
)
)
 (Target 1))
 (Target 2))
 (Target 3))
 (Target 1))
 (Target 2))
 (Target 3))
 ELISA Kit)
)
