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Catalog Number: (10796-714)
Supplier: Bachem Americas
Description: Biotinyl-Amylin (human), Trifluoroacetate salt, Molecular Formula: C175H275N53O57S3, Relative Molecular Mass: 4129.63, CAS Registry Number: [1678415-18-3] net, Source: Synthetic, Storage Conditions: -20 +/- 5 degree Celcius, 0.5mg


Catalog Number: (L-1240.0050BA)
Supplier: Bachem Americas
Description: Z-KR-pNA, CAS-number (net) 108318-37-2.


Catalog Number: (76110-620)
Supplier: Bioss
Description: NET-4, also known as TSPAN5 or TM4SF9, is a 268 amino acid multi-pass membrane protein that belongs to the tetraspanin family and is thought to play a role in signal transduction events related to cell development, activation, growth and motility. The gene encoding NET-4 maps to human chromosome 4, which encodes nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.


Catalog Number: (76855-772)
Supplier: ANTIBODIES.COM LLC
Description: Rabbit polyclonal antibody to Eph receptor B1 / NET for WB with samples derived from Human and Mouse.


Catalog Number: (77128-280)
Supplier: Prosci
Description: Anti-TSPAN5/NET-4 Goat Polyclonal Antibody


Catalog Number: (10002-034)
Supplier: ELPRO SERVICES, INC.
Description: ECOLOG-NET Central Monitoring System is your solution for compliant monitoring offered in a Wireless, Wired or hybrid setup It is a redundant, scalable system that can grow according to user needs, whether monitoring just a few or several hundred pieces of laboratory equipment or other critical environments (such as storage spaces or LN2 tanks)


Catalog Number: (10487-774)
Supplier: Bioss
Description: NET-4, also known as TSPAN5 or TM4SF9, is a 268 amino acid multi-pass membrane protein that belongs to the tetraspanin family and is thought to play a role in signal transduction events related to cell development, activation, growth and motility. The gene encoding NET-4 maps to human chromosome 4, which encodes nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.


Catalog Number: (10489-692)
Supplier: Bioss
Description: NET-4, also known as TSPAN5 or TM4SF9, is a 268 amino acid multi-pass membrane protein that belongs to the tetraspanin family and is thought to play a role in signal transduction events related to cell development, activation, growth and motility. The gene encoding NET-4 maps to human chromosome 4, which encodes nearly 6% of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.


Supplier: Abcam
Description: Anti-Eph receptor B1/NET Rabbit Monoclonal Antibody [clone: EPR6457]

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Supplier: Bachem Americas
Description: [6366-77-4] (net)

Catalog Number: (76109-310)
Supplier: Bioss
Description: The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 encodes over 1100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.


Supplier: Ace Glass
Description: This heavy-wall borosilicate glass bottle has three PTFE valves with Tefzel keys.

Small Business Enterprise Product available on GSA Advantage®

Supplier: Sklar
Description: All Sklar products are industry standard.

Catalog Number: (10487-836)
Supplier: Bioss
Description: NET-6, also known as TSPAN13 (tetraspanin-13) or TM4SF13 (transmembrane 4 superfamily member 13), is a 204 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. Members of the tetraspanin family are cell-surface proteins that are characterized by the presence of four hydrophobic domains and mediate signal transduction events that play a role in the regulation of cell development, activation, growth, motility, differentiation, and cancer. Considered molecular facilitators, tetraspanin proteins may regulate vesicle fusion and fission. The gene encoding NET-6 maps to human chromosome 7, which houses over 1,000 genes, comprises nearly 5% of the human genome and has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.


Catalog Number: (10488-086)
Supplier: Bioss
Description: The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.


Catalog Number: (10487-852)
Supplier: Bioss
Description: NET-6, also known as TSPAN13 (tetraspanin-13) or TM4SF13 (transmembrane 4 superfamily member 13), is a 204 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. Members of the tetraspanin family are cell-surface proteins that are characterized by the presence of four hydrophobic domains and mediate signal transduction events that play a role in the regulation of cell development, activation, growth, motility, differentiation, and cancer. Considered molecular facilitators, tetraspanin proteins may regulate vesicle fusion and fission. The gene encoding NET-6 maps to human chromosome 7, which houses over 1,000 genes, comprises nearly 5% of the human genome and has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.


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