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PARS2 antibody
PARS2
Reactivity: Human, Mouse, Rat
ELISA, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-PARS2 Antibody
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Target
See all PARS2 Antibodies
PARS2
(Prolyl-tRNA Synthetase 2, Mitochondrial (Putative) (PARS2))
Reactivity
All reactivities for PARS2 antibodies
Human, Mouse, Rat
Host
All hosts for PARS2 antibodies
Rabbit
Clonality
All clonalities for PARS2 antibodies
Polyclonal
Conjugate
All conjugates for PARS2 antibodies
This PARS2 antibody is un-conjugated
Application
All applications for PARS2 antibodies
ELISA, Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Antigen affinity purification
Immunogen
Fusion protein of human PARS2
Isotype
IgG
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Discover our top product PARS2 Primary Antibody
Alternatives
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Application Details
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Application Notes
IHC 1:30-1:150, ELISA 1:5000-1:10000
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.96 mg/mL
Buffer
PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for PARS2
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Target
PARS2
(Prolyl-tRNA Synthetase 2, Mitochondrial (Putative) (PARS2))
Alternative Name
PARS2 (PARS2 Products )
Synonyms
fc83e06 antibody, zgc:77163 antibody, wu:fc83e06 antibody, MGC53152 antibody, BC027073 antibody, MT-PRORS antibody, RGD1305345 antibody, prolyl-tRNA synthetase 2, mitochondrial antibody, prolyl-tRNA synthetase 2, mitochondrial L homeolog antibody, prolyl-tRNA synthetase 2, mitochondrial (putative) antibody, prolyl-tRNA synthetase 2, mitochondria antibody, prolyl-tRNA synthetase (mitochondrial)(putative) antibody, pars2 antibody, pars2.L antibody, PARS2 antibody, Pars2 antibody
Background
This gene encodes a putative member of the class II family of aminoacyl-tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. This protein is encoded by the nuclear genome but is likely to be imported to the mitochondrion where it is thought to catalyze the ligation of proline to tRNA molecules. Mutations have been found in this gene in some patients with Alpers syndrome.
UniProt
Q7L3T8
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