The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
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Shipped at 4°C. Store at -20°C.
Constituents: 0.32% Tris HCl, 0.58% Sodium chloride
Reconstitute with water to desired concentration.
Acid sensing ion channel 3
Acid-sensing ion channel 3
Amiloride sensitive cation channel 3
Amiloride sensitive cation channel 3 testis
Amiloride-sensitive cation channel 3
Modulatory subunit of ASIC 2a
Modulatory subunit of ASIC2a
Neuronal amiloride sensitive cation channel 3
Neuronal amiloride-sensitive cation channel 3
Proton gated cation channel subunit
Testis sodium channel 1
Cation channel with high affinity for sodium, which is gated by extracellular protons and inhibited by the diuretic amiloride. Generates a biphasic current with a fast inactivating and a slow sustained phase. In sensory neurons is proposed to mediate the pain induced by acidosis that occurs in ischemic, damaged or inflamed tissue. May be involved in hyperalgesia. May play a role in mechanoreception. Heteromeric channel assembly seems to modulate channel properties.
Expressed by sensory neurons. Strongly expressed in brain, spinal chord, lung, lymph nodes, kidney, pituitary, heart and testis.
Belongs to the amiloride-sensitive sodium channel (TC 1.A.6) family. ACCN3 subfamily.
Expressed in fetal tissues, expression increases in lung and kidney adult tissues.
The PDZ domain-binding motif is involved in interaction with LIN7A, GOPC and MAGI1.
Phosphorylated by PKA. Phosphorylated by PKC. In vitro, PRKCABP/PICK-1 is necessary for PKC phosphorylation and activation of a ACCN3/ASIC3-ACCN1/ASIC2b channel, but does not activate a homomeric ACCN3 channel.
Cell membrane. Cytoplasm. Cell surface expression may be stabilized by interaction with LIN7B and cytoplasmic retention by interaction with DLG4. In part cytoplasmic in cochlea cells.