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液泡膜质子转运ATP酶2型抗体
交货期:1周


产品名称
Anti-Atp6v0a2
Anti-ATPase, H+ transporting, lysosomal V0 subunit A2 Antibody
产品介绍
靶标:

Atp6v0a2


产品别名:

8430408C20Rik; AI385560; ATP6a2; AW489264; Atp6n1d; Atp6n2; C76904; ISF; J6B7; SHIF; Stv1; TJ6M; TJ6s; Tj6; V-ATPase 116 kDa; V-ATPase a2; Atp6v0a2; ATPase, H+ transporting, lysosomal V0 subunit A2; ATPase, H+ transporting, lysosomal V0 subunit A2; V-type proton ATPase 116 kDa subunit a 2; ATPase, H+ transporting, lysosomal (vacuolar proton pump) non-catalytic accessory protein 2 (38kD); ATPase, H+ transporting, lysosomal V0 subunit a; T-cell expressing clone j6; V-ATPase 116 kDa subunit a 2; V-ATPase 116 kDa subunit a2; V-type proton ATPase 116 kDa subunit a; V-type proton ATPase 116 kDa subunit a2; immune suppressor factor J6B7; lysosomal H(+)-transporting ATPase V0 subunit a 2; vacuolar proton translocating ATPase 116 kDa subunit a; 液泡膜质子转运ATP酶2型;


背景信息:
The protein encoded by this gene is a subunit of the vacuolar ATPase (v-ATPase), an heteromultimeric enzyme that is present in intracellular vesicles and in the plasma membrane of specialized cells, and which is essential for the acidification of diverse cellular components. V-ATPase is comprised of a membrane peripheral V(1) domain for ATP hydrolysis, and an integral membrane V(0) domain for proton translocation. The subunit encoded by this gene is a component of the V(0) domain. Mutations in this gene are a cause of both cutis laxa type II and wrinkly skin syndrome. [provided by RefSeq, Jul 2009],
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