Primary antibodies

Primary antibodies

Descrizione	Azione
TRPV3 Antibody detects endogenous levels of total TRPV3. TRPV3 Antibody Codice: DF10186 Confezionamento: 200ul	Dettagli
TRPV3 Antibody detects endogenous levels of total TRPV3. TRPV3 Mouse Monoclonal Antibody Codice: BF8081 Confezionamento: 200ul	Dettagli
TRPV3 Antibody detects endogenous levels of total TRPV3. TRPV3 Mouse Monoclonal Antibody Codice: BF8081 Confezionamento: 100ul	Dettagli
TRPV4 Antibody detects endogenous levels of total TRPV4. TRPV4 Antibody Codice: DF8624 Confezionamento: 100ul	Dettagli
TRPV4 Antibody detects endogenous levels of total TRPV4. TRPV4 Antibody Codice: DF8624 Confezionamento: 200ul	Dettagli
This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene. TRPV4 Polyclonal Antibody Codice: E-AB-14424_200μL Confezionamento: 200μL	Dettagli
This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene. TRPV4 Polyclonal Antibody Codice: E-AB-14424_20μL Confezionamento: 20μL	Dettagli
This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene. TRPV4 Polyclonal Antibody Codice: E-AB-14424_60μL Confezionamento: 60μL	Dettagli
This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene. TRPV4 Polyclonal Antibody Codice: E-AB-14424_120μL Confezionamento: 120μL	Dettagli
This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene. TRPV4 Polyclonal Antibody Codice: E-AB-10664_120μL Confezionamento: 120μL	Dettagli
This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene. TRPV4 Polyclonal Antibody Codice: E-AB-10664_60μL Confezionamento: 60μL	Dettagli
This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene. TRPV4 Polyclonal Antibody Codice: E-AB-10664_20μL Confezionamento: 20μL	Dettagli

1…6333 6334 633563366337 6338 6339…6620

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