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Numéro de catalogue: (BOSSBS-5343R-CY7)

Fournisseur:  Bioss
Description:   This gene is a member of the Tyr protein kinase family and the epidermal growth factor receptor subfamily. It encodes a single-pass type I membrane protein with multiple cysteine rich domains, a transmembrane domain, a tyrosine kinase domain, a phosphotidylinositol-3 kinase binding site and a PDZ domain binding motif. The protein binds to and is activated by neuregulins and other factors and induces a variety of cellular responses including mitogenesis and differentiation. Multiple proteolytic events allow for the release of a cytoplasmic fragment and an extracellular fragment. Mutations in this gene have been associated with cancer. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008].
UOM:  1 * 100 µl
Numéro de catalogue: (BOSSBS-11395R)

Fournisseur:  Bioss
Description:   Syntaxins were originally thought to be docking proteins, but have more recently been categorized as anchoring proteins that anchor themselves to the cytoplasmic surfaces of cellular membranes. Syntaxins bind to various proteins involved in exocytosis, including VAMPs (vesicle-associated membrane proteins), NSF (N-ethylmaleimide-sensitive factor), SNAPs (soluble NSF attachment proteins) and Synaptotagmin. Endobrevin, also designated VAMP-8 or ED, is a 100 amino acid single-pass type IV membrane protein that belongs to the synaptobrevin family. Similar in sequence to the synaptobrevins, endobrevin is abundantly expressed in kidney, moderately expressed in heart and spleen, and slightly expressed in brain, thymus and liver. Endobrevin interacts specifically with the SNAPs, most likely through an endobrevin-containing SNARE complex.
UOM:  1 * 100 µl
Numéro de catalogue: (BOSSBS-10470R-CY5)

Fournisseur:  Bioss
Description:   This gene is a member of the Tyr protein kinase family and the epidermal growth factor receptor subfamily. It encodes a single-pass type I membrane protein with multiple cysteine rich domains, a transmembrane domain, a tyrosine kinase domain, a phosphotidylinositol-3 kinase binding site and a PDZ domain binding motif. The protein binds to and is activated by neuregulins and other factors and induces a variety of cellular responses including mitogenesis and differentiation. Multiple proteolytic events allow for the release of a cytoplasmic fragment and an extracellular fragment. Mutations in this gene have been associated with cancer. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008].
UOM:  1 * 100 µl

Fournisseur:  ENZO LIFE SCIENCES
Description:   Recommended Applications: Flow Cytometry

Species reactivity: Human
UOM:  1 * 1 EA
New Product

Fournisseur:  ENZO LIFE SCIENCES
Description:   Recommended Applications: Flow Cytometry

Species reactivity: Human
UOM:  1 * 1 EA
New Product
Fournisseur:  Saint Gobain Life Sciences
Description:   Pure-Fit SIB eliminates entrapment and leak points that can occur with traditional assembly systems. The unique internal design eliminates voids or dead space that can lead to turbulence or stagnation of fluid flow creating the potential for bacterial growth.
Numéro de catalogue: (BOSSBS-6179R-CY5)

Fournisseur:  Bioss
Description:   Involved in exocytosis by regulating a late step in synaptic vesicle fusion. Could play a role in neurotransmitter release by regulating membrane flow in the nerve terminal.
UOM:  1 * 100 µl
Fournisseur:  WTW
Description:   Sample bottle for IDS turbidity sensor VisoTurb® 900-P, volume 500 ml, Pour: VisoTurb® 900-P
Numéro de catalogue: (BOSSBS-11896R-A555)

Fournisseur:  Bioss
Description:   NETO2 is a 525 amino acid single-pass type I membrane protein that contains two CUB domains and one LDL-receptor class A domain. Expressed as multiple alternatively spliced isoforms, NETO2 is thought to play a role in the development and maintenance of neuronal circuitry, possibly playing a role in proper brain function. The gene encoding NETO2 maps to human chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
UOM:  1 * 100 µl

Fournisseur:  Bioss
Description:   NETO2 is a 525 amino acid single-pass type I membrane protein that contains two CUB domains and one LDL-receptor class A domain. Expressed as multiple alternatively spliced isoforms, NETO2 is thought to play a role in the development and maintenance of neuronal circuitry, possibly playing a role in proper brain function. The gene encoding NETO2 maps to human chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
UOM:  1 * 100 µl
Numéro de catalogue: (BOSSBS-11862R-CY7)

Fournisseur:  Bioss
Description:   DYX2 is a 1072 amino acid single-pass transmembrane protein that contains one MANSC domain and two PKD (Polycystic Kidney Disease) domains, which are usually found in the extracellular regions of proteins and are involved in protein-protein interactions. In DYX2, it is likely that its PKD domains mediate the interaction between neurons and glial fibers during neuronal migration. When overexpressed, this plasma membrane protein colocalizes with EEA1 (early endosome antigen 1) in large intracellular vesicles, suggesting that it is endocytosed and recycled. DYX2 is highly expressed in brain cortex, cerebellum, amygdala, putamen and hippocampus. Defects in the gene encoding DYX2 may be the cause of dyslexia type 2, a relatively common disorder that is characterized by reading performance impairment in the absence of sensory or neurologic disability. There are three isoforms of DYX2 that are produced as a result of alternative splicing events
UOM:  1 * 100 µl
Numéro de catalogue: (NOVUNB120-15680)

Fournisseur:  Novus Biologicals
Description:   Rat Monoclonal MHC Class I Antibody (ERMP42). Tested Applications: Flow Cytometry, Immunohistochemistry, Immunohistochemistry-Frozen. Tested Reactivity: Mouse, Human (-).
UOM:  1 * 50 µG
Numéro de catalogue: (MLDV5084788)

Fournisseur:  Molecular Devices
Description:   Photodocumentation System, Gas mixer for ImageXpress® systems (Mixes 100% CO₂ with air to deliver 5% CO₂ into the sample chamber; flow and mixture are electronically controlled and stabilised for healthy and accurate long term time lapses of living cells)
UOM:  1 * 1 ST
Numéro de catalogue: (634-0759)

Fournisseur:  VWR Collection
Description:   Accessoire pour spectrophotomètre UV/Vis, Porte-cuvette unique avec parcours optique de 10 mm, Pour: U-5100
UOM:  1 * 1 ST
Numéro de catalogue: (ROCK712-1133)

Fournisseur:  Rockland Immunochemicals
Description:   Suitable for immunomicroscopy and flow cytometry or FACS analysis as well as other antibody based fluorescent assays requiring extremely low background levels, absence of F(c) mediated binding, lot-to-lot consistency, high titer and specificity.
UOM:  1 * 500 µG
Numéro de catalogue: (ROCK712-701-149)

Fournisseur:  Rockland Immunochemicals
Description:   Suitable for immunomicroscopy and flow cytometry or FACS analysis as well as other antibody based fluorescent assays requiring extremely low background levels, absence of F(c) mediated binding, lot-to-lot consistency, high titer and specificity.
UOM:  1 * 500 µG
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