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  2. Polyclonal

GTX31567

TRPV4 antibody

Cannot supply to this region.

SKU:
GTX31567
Additional Names:
transient receptor potential cation channel subfamily V member 4 , BCYM3 , CMT2C , HMSN2C , OTRPC4 , SMAL , SPSMA , SSQTL1 , TRP12 , VRL2 , VROAC
Application:
ELISA, WB, IHC-P
Concentration:
1 mg/ml
Physical State:
Liquid
Species Reactivity:
Human
Purification:
Affinity Purified
Storage Conditions:
-20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:
Genetex
Host:
Rabbit
Reactivities:
Human
Buffer:
PBS, 0.02% Sodium azide.
Immunogen:
TRPV4 antibody was raised against an 18 amino acid peptide near the center of human TRPV4.The immunogen is located within amino acids 380 - 430 of TRPV4.
Uniprot:
Q9HBA0
Synonyms:
BCYM3;CMT2C;HMSN2C;osm-9-like TRP channel 4;OSM9-like transient receptor potential channel 4;osmosensitive transient receptor potential channel 4;OTRPC4;SMAL;SPSMA;SSQTL1;transient receptor potential cation channel subfamily V member 4;transient receptor potential protein 12;TRP12;vanilloid receptor-like channel 2;Vanilloid receptor-like protein 2;vanilloid receptor-related osmotically activated channel;Vanilloid receptor-related osmotically-activated channel;VRL2;VROAC
Extra Details:
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. [provided by RefSeq, Apr 2010]
Shipping Conditions:
Blue Ice