ATP13A2 产品
(ATPase Type 13A2 (ATP13A2))
Categories
This gene encodes a member of the P5 subfamily of ATPases which transports inorganic cations as well as other substrates. Mutations in this gene are associated with Kufor-Rakeb syndrome (KRS), also referred to as Parkinson disease 9. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2008].
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Featured ATP13A2 Categories
ATP13A2 抗体
High quality antibodies with extensive validation data.
ATP13A2 ELISA试剂盒
Reliable ELISA kits for a wide range of species.
ATP13A2 蛋白
Proteins for various applications incl. WB, ELISA, IF etc.
Recommended ATP13A2 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
ELISA, WB
Validations
- (2)
Cat. No.
ABIN525142
Quantity
100 μg
Datasheet
Datasheet
Reactivity
Rat
Application
ELISA, IF (cc), IF (p), IHC (fro), IHC (p), ICC
Validations
- (1)
Cat. No.
ABIN1387850
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human
Application
ELISA, IF
Validations
- (1)
Cat. No.
ABIN7147051
Quantity
100 μL
Datasheet
Datasheet
Recommended ATP13A2 ELISA试剂盒
Product
Reactivity
Analytical Method
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Analytical Method
Quantitative Competition ELISA
Validations
Cat. No.
ABIN5591580
Quantity
96 tests
Datasheet
Datasheet
Reactivity
Mouse
Analytical Method
Quantitative Sandwich ELISA
Validations
Cat. No.
ABIN5591581
Quantity
96 tests
Datasheet
Datasheet
Recommended ATP13A2 蛋白
Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Source
Wheat germ
Validations
- (1)
Cat. No.
ABIN1346016
Quantity
10 μg
Datasheet
Datasheet
Reactivity
Human
Source
Tobacco (Nicotiana tabacum)
Validations
Cat. No.
ABIN3118379
Quantity
1 mg
Datasheet
Datasheet
Reactivity
Mouse
Source
Tobacco (Nicotiana tabacum)
Validations
Cat. No.
ABIN3137038
Quantity
1 mg
Datasheet
Datasheet
Latest Publications for our ATP13A2 Products
: "Pathogenic LRRK2 mutations, through increased kinase activity, produce enlarged lysosomes with reduced degradative capacity and increase ATP13A2 expression." in: Human molecular genetics, Vol. 24, Issue 21, pp. 6013-28, (2015) (PubMed).: "Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 109, Issue 24, pp. 9611-6, (2012) (PubMed).
: "Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase." in: Nature genetics, Vol. 38, Issue 10, pp. 1184-91, (2006) (PubMed).
Synonyms and alternative names related to ATP13A2
ATPase 13A2 (ATP13A2), ATPase type 13A2 (Atp13a2), ATPase 13A2 (Atp13a2), ATPase type 13A2 (atp13a2), ATPase type 13A2 (PTRG_01071), ATPase type 13A2 (MCYG_01937), probable cation-transporting ATPase 13A2 (LOC100439053), 1110012E06Rik, AA589443, ATP13A2, CLN12, HSA9947, im:7147302, KRPPD, PARK9, RGD1307977, zgc:136762Protein level used designations for ATP13A2
- ATPase type 13A2
- probable cation-transporting ATPase 13A2
- N-ATPase
- putative ATPase
- probable cation-transporting ATPase 13A2-like
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