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ATP13A2 Rabbit Polyclonal Antibody

CAT: 0013-GTR17744439-01Size: 50 μLDry Ice: NoHazardous: No
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CAT#:0013-GTR17744439-01Size:50 μL
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Description
ATP13A2 Rabbit Polyclonal Antibody
Product Name Alternative
CLN12; HSA9947; KRPPD; PARK9; SPG78; 1110012E06Rik; RGD1307977; AT132_HUMAN; ATP13A2; 7.6.2.-; AT132_MOUSE; ATPase cation transporting 13A2; Parkinson disease (autosomal recessive) 9 (Kufor-Rakeb syndrome) ; ATPase type 13A2; ATPase 13A2
UniProt
Q9NQ11
Reactivity
Rat
Immunogen
KLH conjugated synthetic peptide derived from human ATP13A2 (1001-1080/1180aa)
Target
ATP13A2
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Neuroscience
Purification
Affinity purified by Protein A
Concentration
1mg/ml
Dilution
IHC-P=1:100-500, IHC-F=1:100-500, IF=1:100-500
Form
Liquid
Molecular Weight
129 kDa
References & Citations
Chen, Qian et al. Knockdown of Parkinson's disease-related gene ATP13A2 reduces tumorigenesis via blocking autophagic flux in colon cancer Cell Biosci, 10, 144 (2020)
Pubmed id
33308286
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Notes
For research use only.
Prediction Reactivity
Bovine, Equine, Human, Mouse, Porcine, Rabbit
Tested Applications
IF, IHC-Fr, IHC-P
Host or Source
Rabbit
Preservative
0.01M TBS (pH7.4) with 1% rAlbumin, 0.02% Proclin300 and 50% Glycerol.
Isotype
IgG

UniProtKB · Q9NQ11

Polyamine-transporting ATPase 13A2

AT132_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9NQ11
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
ATP13A2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
7.6.2.-
Processing
—
Secondary accessions
O75700, Q5JXY1, Q5JXY2, Q6S9Z9
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Ligand

ATP-bindingLipid-bindingMagnesiumMetal-bindingNucleotide-binding

Cellular component

Cytoplasmic vesicleEndosomeLysosomeMembrane

Disease

Disease variantHereditary spastic paraplegiaNeurodegenerationNeuronal ceroid lipofuscinosisParkinsonism

PTM

GlycoproteinPhosphoprotein

Molecular function

Translocase

Domain

TransmembraneTransmembrane helix

Biological process

Transport

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