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Rabbit anti-Human VARS2 Polyclonal Antibody

The antibody against VARS2 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 864-1063 of human VARS2 (NP_065175.4) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

ADA-05023A

The antibody against VARS2 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 864-1063 of human VARS2 (NP_065175.4) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

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Specifications


Cat.No ADA-05023A ClonalityPolyclonal
Host SpeciesRabbitTarget NameVARS2
Target SynonymsVALRS; VARSL; VARS2L; COXPD20; VARS2FormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.01% thimerosal, pH7.3.Purification MethodAffinity purification
Positive SamplesU-251MGApplicationELISA, WB

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 864-1063 of human VARS2 (NP_065175.4).Target SpeciesHuman
Immunogen SequenceLWQRLPPRPGCPPAPSISVAPYPSACSLEHWRQPELERRFSRVQEVVQVLRALRATYQLTKARPRVLLQSSEPGDQGLFEAFLEPLGTLGYCGAVGLLPPGAAAPSGWAQAPLSDTAQVYMELQGLVDPQIQLPLLAARRYKLQKQLDSLTARTPSEGEAGTQRQQKLSSLQLELSKLDKAASHLRQLMDEPPAPGSPELUniprot IDQ5ST30
Background Information
  • Uniprot Id

    Q5ST30

  • Target Species

    Human

  • Target Name

    VARS2

  • Target Full Name

    Valine--tRNA ligase, mitochondrial

  • Target Involvement

    Combined oxidative phosphorylation deficiency 20 (COXPD20)

  • Target Subcellular Location

    Mitochondrion.

  • Target Protein Families

    Class-I aminoacyl-tRNA synthetase family

  • Target Synonyms

    COXPD20; mitochondrial; SYVM_HUMAN; Valine--tRNA ligase; ValRS; Valyl tRNA synthetase 2 mitochondrial; Valyl-tRNA synthetase; Valyl-tRNA synthetase-like; Vars2; VARS2L; VARSL

  • Target Background

    This gene encodes a mitochondrial aminoacyl-tRNA synthetase, which catalyzes the attachment of valine to tRNA(Val) for mitochondrial translation. Mutations in this gene cause combined oxidative phosphorylation deficiency-20, and are also associated with early-onset mitochondrial encephalopathies. Alternative splicing of this gene results in multiple transcript variants.

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