12003 Results for: "GUANGZHOU+JET+BIOFILTRATION&pageNo=21&view=list"
Eco Hi-Vis Work Trousers
Supplier: Portwest
A classic style with a full update, made from a sustainable polyester/cotton fabric.
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Real-Time PCR kit for detection of toxic Vibrio cholerae
Supplier: Q BIOANALYTIC
Kit for Vibrio cholerae tox gene (ctx). Food safety experts like the German DGHM recommend to test warm water fish for vibrio cholerae. With this Real-Time PCR test you have a very versatile method for testing whether or not the present strain has the ability to produce toxins. You can use our Real-Time PCR Test for Vibrio cholerae for testing for the presence of the species before. You can use this test in combination with an appropriate pre- enrichment in alkaline peptone-water or you can confirm bacterial colonies on agar plates.
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Human MYH7B ELISA Kit
Supplier: Antibodies.com
Human MYH7B ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human MYH7B in serum, plasma, and other biological fluids.
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Human DR6 ELISA Kit
Supplier: Antibodies.com
Human DR6 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human DR6 in serum, plasma, tissue homogenates, and other biological fluids.
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Human PTTG1IP ELISA Kit
Supplier: Antibodies.com
Human PTTG1IP ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human PTTG1IP in serum, plasma, tissue homogenates, and other biological fluids.
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Human LY6G6D ELISA Kit
Supplier: Antibodies.com
Human LY6G6D ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human LY6G6D in serum, plasma, and other biological fluids.
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Human DR6 ELISA Kit
Supplier: Antibodies.com
Human DR6 ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human DR6 in serum, plasma, and other biological fluids.
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Human POTED ELISA Kit
Supplier: Antibodies.com
Human POTED ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human POTED in serum, plasma, and other biological fluids.
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Micro-quartz fibre filters
Supplier: Ahlstrom-Munksjö
Micro-quartz filters are useful for testing hot "stack" gases as the quartz fibers can withstand temperatures up to 900 °C. In addition, micro-quartz is used when the highest purity media is required. With excellent filtration properties and minimal traces of metals and minerals, quartz fibers are dimensionally stable and can be used in the analysis of acidic gases with the exception of hydrofluoric acid.
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Rectangle Cryogenic Labels for Thermal Transfer Barcode Printers
Supplier: GA
These labels are available in a range of sizes and configurations, perfect for identifying small diameter cryo vials, microtubes, cardboard or polypropylene cryo/freezer boxes, cell culture plates, and plastic bags.
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Trousers, PW3, T601 Urban Work
Supplier: Portwest
Rugged trouser made from durable Kingsmill polyester/cotton 300 g fabric with a modern fit and adjustable leg length. Pockets have oxford reinforcement for extra durability.
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UltraSpeed cleaning system
Supplier: FHP VILEDA SCS
The UltraSpeed system is designed to save time whilst reducing the floor cleaning costs in all general building and HoReCa environments, irrespective of size with or without laundry facilities. The system easily covers all cleaning requirements - the mops and frame can be used with a 25 l single bucket or 2×25 l double bucket on wheels depending on the size of your area. The mops and frames are versatile and can be used to clean floors, skirting boards, walls, staircases and ceilings.
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Welding trousers with waistband, Flam
Supplier: FRISTADS KANSAS
Protective trousers made from 75% cotton and 25% polyester. The cotton/polyester fabric mix offers long lasting protection against open flames and sources of heat thanks to the flame-retardant used.
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Trousers, Fristads® PR54-220, Design B, Royal Blue
Supplier: FRISTADS KANSAS
Thanks to their durability and comfort, these trousers are perfectly suitable for use in garages as well as in industrial and service companies. The material is made of 65% polyester and 35% cotton. The inside is brushed and provides a comfortable cotton feel. The outside is very hardwearing and does not bleach, even after countless washes.
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Cleanroom gloves, polychloroprene, DermaShield® 73-711 / 73-721
Supplier: Ansell
Hand-specific, ergonomically designed gloves with a beaded cuff. Ideal for use in laboratories, pharmaceutical, biotech and medical device manufacturing.
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Anti-FBXL21 Rabbit Polyclonal Antibody (Cy3®)
Supplier: Bioss
FBL3B is a 434 amino acid protein encoded by the human gene FBXL21. FBL3B contains one 40 amino acid F-box region, making it a member of the F-box family. FBL3B also contains three LRR (leucine-rich) repeats. F-box proteins are critical components of the SCF (Skp1-CUL-1-F-box protein) type E3 ubiquitin ligase complex and are involved in substrate recognition and recruitment for ubiquitination. F-box proteins are members of a large family that regulates cell cycle, immune response, signaling cascades and developmental programs by targeting proteins, such as cyclins, cyclin-dependent kinase inhibitors, IkB-a and b-catenin, for degradation by the proteasome after ubiquitination. FBL3B is a substrate-recognition component of the SCF complex that interacts with Skp1 p19 and CUL-1. FBL3B is also associated with expression and regulation of circadian and cryptochrome proteins.
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Anti-AMHR2 Rabbit Polyclonal Antibody (Alexa Fluor® 680)
Supplier: Bioss
MISR II is a 573 amino acid protein encoded by the human gene AMHR2. MISR II belongs to the protein kinase superfamily, TKL Ser/Thr protein kinase family, TGFB receptor subfamily and contains one protein kinase domain. Upon ligand binding, MISR II forms a receptor complex consisting of two type II and two type I transmembrane serine/threonine kinases. These type II receptors rylate and activate type I receptors which autophosphorylate, then bind and activate Smad transcriptional regulators. MISR II also acts as a receptor for anti-Muellerian hormone. Defects in AMHR2 are the cause of persistent Muellerian duct syndrome type 2 (PMDS-2). PMDS-2 is a form of male pseudo-hermaphroditism characterised by a failure of Muellerian duct regression in otherwise normal males.
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Anti-FBXL21 Rabbit Polyclonal Antibody (Alexa Fluor® 647)
Supplier: Bioss
FBL3B is a 434 amino acid protein encoded by the human gene FBXL21. FBL3B contains one 40 amino acid F-box region, making it a member of the F-box family. FBL3B also contains three LRR (leucine-rich) repeats. F-box proteins are critical components of the SCF (Skp1-CUL-1-F-box protein) type E3 ubiquitin ligase complex and are involved in substrate recognition and recruitment for ubiquitination. F-box proteins are members of a large family that regulates cell cycle, immune response, signaling cascades and developmental programs by targeting proteins, such as cyclins, cyclin-dependent kinase inhibitors, IkB-a and b-catenin, for degradation by the proteasome after ubiquitination. FBL3B is a substrate-recognition component of the SCF complex that interacts with Skp1 p19 and CUL-1. FBL3B is also associated with expression and regulation of circadian and cryptochrome proteins.
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Anti-NeuroD1 Rabbit Polyclonal Antibody (HRP (Horseradish PE (Phycoerythrin)rOxidase))
Supplier: Bioss
Acts as a transcriptional activator: mediates transcriptional activation by binding to E box-containing promoter consensus core sequences 5'-CANNTG-3'. Associates with the p300/CBP transcription coactivator complex to stimulate transcription of the secretin gene as well as the gene encoding the cyclin-dependent kinase inhibitor CDKN1A. Contributes to the regulation of several cell differentiation pathways, like those that promote the formation of early retinal ganglion cells, inner ear sensory neurons, granule cells forming either the cerebellum or the dentate gyrus cell layer of the hippocampus, endocrine islet cells of the pancreas and enteroendocrine cells of the small intestine. Together with PAX6 or SIX3, is required for the regulation of amacrine cell fate specification. Also required for dendrite morphogenesis and maintenance in the cerebellar cortex. Associates with chromatin to enhancer regulatory elements in genes encoding key transcriptional regulators of neurogenesis (By similarity).
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Dialysis systems Spectra/Por® Float-A-Lyzer® G2
Supplier: Spectrum Laboratories
Ready-to-use laboratory dialysis systems featuring proprietary Ultra-pure Biotech Cellulose Ester (CE) Membrane. Biotech Grade CE is a low protein-binding synthetic membrane available in 9 precise MWCO's with no heavy metal and sulfide contaminants. The cylindrical tubing geometry prevents sample dilution (associated with cassette-type devices) and provides open access for total volume retrieval by pipette. Only the Float-A-Lyzer® G2 assures a 95 to 98% sample recovery while maintaining 99% sample purity and <1% sample dilution. The leakproof screw-on cap with sealing o-ring provides easy access with included pipette for loading, in-process testing and sample retrieval, without the risk of needle punctures. The included floatation ring improves sample buoyancy and vertical orientation during dialysis. The sleek design allows multiple samples to be dialysed in the same reservoir.
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Anti-C2orf61 Rabbit Polyclonal Antibody (Alexa Fluor® 680)
Supplier: Bioss
C2orf61 (chromosome 2 open reading frame 61), also known as FLJ40172, is a 177 amino acid protein encoded by a gene that maps to human chromosome 2p21. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
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FARRAR® 4000 Series Controlled Rate Freeze/Thaw Chambers
Supplier: TRANE TECHNOLOGIES
Eliminate uncertainty in your freeze-thaw processes. Purpose-built for bio-processing applications, the Controlled Rate Chamber Model 4000 offers uniformity and repeatability in rapid, controlled freezing and thawing applications. The forced air convection cooling rapidly freezes material from ambient to −80 °C.
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Anti-NeuroD1 Rabbit Polyclonal Antibody (Cy7®)
Supplier: Bioss
Acts as a transcriptional activator: mediates transcriptional activation by binding to E box-containing promoter consensus core sequences 5'-CANNTG-3'. Associates with the p300/CBP transcription coactivator complex to stimulate transcription of the secretin gene as well as the gene encoding the cyclin-dependent kinase inhibitor CDKN1A. Contributes to the regulation of several cell differentiation pathways, like those that promote the formation of early retinal ganglion cells, inner ear sensory neurons, granule cells forming either the cerebellum or the dentate gyrus cell layer of the hippocampus, endocrine islet cells of the pancreas and enteroendocrine cells of the small intestine. Together with PAX6 or SIX3, is required for the regulation of amacrine cell fate specification. Also required for dendrite morphogenesis and maintenance in the cerebellar cortex. Associates with chromatin to enhancer regulatory elements in genes encoding key transcriptional regulators of neurogenesis (By similarity).
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Anti-NeuroD1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)
Supplier: Bioss
Acts as a transcriptional activator: mediates transcriptional activation by binding to E box-containing promoter consensus core sequences 5'-CANNTG-3'. Associates with the p300/CBP transcription coactivator complex to stimulate transcription of the secretin gene as well as the gene encoding the cyclin-dependent kinase inhibitor CDKN1A. Contributes to the regulation of several cell differentiation pathways, like those that promote the formation of early retinal ganglion cells, inner ear sensory neurons, granule cells forming either the cerebellum or the dentate gyrus cell layer of the hippocampus, endocrine islet cells of the pancreas and enteroendocrine cells of the small intestine. Together with PAX6 or SIX3, is required for the regulation of amacrine cell fate specification. Also required for dendrite morphogenesis and maintenance in the cerebellar cortex. Associates with chromatin to enhancer regulatory elements in genes encoding key transcriptional regulators of neurogenesis (By similarity).
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Anti-NeuroD1 Rabbit Polyclonal Antibody (Alexa Fluor® 680)
Supplier: Bioss
Acts as a transcriptional activator: mediates transcriptional activation by binding to E box-containing promoter consensus core sequences 5'-CANNTG-3'. Associates with the p300/CBP transcription coactivator complex to stimulate transcription of the secretin gene as well as the gene encoding the cyclin-dependent kinase inhibitor CDKN1A. Contributes to the regulation of several cell differentiation pathways, like those that promote the formation of early retinal ganglion cells, inner ear sensory neurons, granule cells forming either the cerebellum or the dentate gyrus cell layer of the hippocampus, endocrine islet cells of the pancreas and enteroendocrine cells of the small intestine. Together with PAX6 or SIX3, is required for the regulation of amacrine cell fate specification. Also required for dendrite morphogenesis and maintenance in the cerebellar cortex. Associates with chromatin to enhancer regulatory elements in genes encoding key transcriptional regulators of neurogenesis (By similarity).
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Anti-BIN2 Rabbit Polyclonal Antibody (Alexa Fluor® 750)
Supplier: Bioss
BAR proteins are characterised by a common N-terminal BAR (bin, amphiphysin and Rvs161/167) domain and are recognised as adaptor proteins that are involved in many cellular processes. BIN1 and BIN2 are BAR proteins that share 61% sequence similarity. BIN1 (Bridging integrator 1) is a ubiquitously expressed regulatory protein for synaptic vesicle endocytosis. BIN1 also interacts with the transcription factors c-Myc and MyoD, potentially functioning as a tumour suppressor. BIN2, also known as Breast cancer-associated protein 1, is a 565 amino acid protein that interacts with BIN1. In contrast to BIN1, BIN2 lacks tumour suppressor features as well as a c-Myc interacting region. BIN2 shows preferred expression in tissues of hematopoietic origin, with high levels found in spleen, thymus, colon, placenta, lymphoid and granulocytic cells. There are two isoforms of BIN2 that are produced as a result of alternative splicing events.
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Winlog.Validation Evaluation Software for Ebro Data Loggers EBI 12, EBI 11 and EBI 16
Supplier: EBRO
The easy-to-use software products are suitable for programming and read-out of Ebro® data loggers as well as for the evaluation of the measured values. For routine checks and validation.
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Anti-ELK4/SAP-1a Rabbit Polyclonal Antibody (Alexa Fluor® 750)
Supplier: Bioss
Serum response factor (SRF) is a transcription factor that binds the serum response element (SRE), a sequence that mediates the transient response of many cellular genes to growth stimulation. SRF-binding sites are also constitutive promoter elements in many muscle-specific promoters. At the c-Fos SRE, formation of a ternary complex containing SRF and its accessory protein p62TCF appears to be important for signal transduction. Two related Ets domain proteins, Elk-1 and SRF accessory protein-1 (SAP-1), have DNA binding properties identical to that of p62TCF. Elk-1 and SAP-1 contain two homologous regions of which the two amino terminal regions, the Ets domain (box A) and the B box, mediate ternary complex formation with SRF. The third homologous region, the C box located toward the C-terminus of the proteins, contains conserved consensus phosphorylation sites for MAP kinases.
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Anti-C9orf152 Rabbit Polyclonal Antibody (Alexa Fluor® 680)
Supplier: Bioss
C9orf152 is a 239 amino acid protein encoded by a gene that maps to human chromosome 9q31.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukaemias.
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Anti-C11ORF46 Rabbit Polyclonal Antibody (Alexa Fluor® 680)
Supplier: Bioss
C11orf46, also known as FLJ38968 or dJ299F11.1, is a 260 amino acid protein that is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumours, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.