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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.

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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 IHC, WB
Validations
  • collections(2)
Cat. No. ABIN363562
Quantity 0.1 mL
Reactivity Human
Application ELISA, WB
Validations
  • collections(2)
Cat. No. ABIN525142
Quantity 100 μg
Reactivity Human, Mouse, Rat
Application WB
Validations
  • collections(1)
Cat. No. ABIN6290030
Quantity 50 μL

Recommended ATP13A2 ELISA试剂盒

Product
Reactivity
Analytical Method
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Analytical Method Quantitative Sandwich ELISA
Validations
  • collections(1)
Cat. No. ABIN6965082
Quantity 96 tests
Reactivity Human
Analytical Method Quantitative Competition ELISA
Validations
Cat. No. ABIN5591580
Quantity 96 tests
Reactivity Mouse
Analytical Method Quantitative Sandwich ELISA
Validations
Cat. No. ABIN5591581
Quantity 96 tests

Recommended ATP13A2 蛋白

Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Source Escherichia coli (E. coli)
Validations
  • collections(1)
Cat. No. ABIN3089521
Quantity 1 mg
Reactivity Mouse
Source Escherichia coli (E. coli)
Validations
  • collections(1)
Cat. No. ABIN3128488
Quantity 1 mg
Reactivity Human
Source Insect Cells
Validations
  • collections(1)
Cat. No. ABIN3089522
Quantity 1 mg

Latest Publications on 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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