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ATP13A2 产品

(ATPase Type 13A2 (ATP13A2))
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, Mouse
Application WB, IHC
Validations
  • (1)
  • (2)
Cat. No. ABIN540775
Quantity 100 μL
Datasheet Datasheet
Reactivity Human
Application WB, ELISA
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

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 Mouse
Source Escherichia coli (E. coli)
Validations
  • (1)
Cat. No. ABIN3128488
Quantity 1 mg
Datasheet Datasheet
Reactivity Human
Source Escherichia coli (E. coli)
Validations
  • (1)
Cat. No. ABIN3089521
Quantity 1 mg
Datasheet Datasheet

Latest Publications for our ATP13A2 Products

Henry, Aghamohammadzadeh, Samaroo, Chen, Mou, Needle, Hirst: "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).

Dehay, Ramirez, Martinez-Vicente, Perier, Canron, Doudnikoff, Vital, Vila, Klein, Bezard: "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).

Ramirez, Heimbach, Gründemann, Stiller, Hampshire, Cid, Goebel, Mubaidin, Wriekat, Roeper, Al-Din, Hillmer, Karsak, Liss, Woods, Behrens, Kubisch: "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:136762

Protein 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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