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PRPS1 Antibody

CAT: 0864-A32132-50ULSize: 50 μLDry Ice: NoHazardous: No
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CAT#:0864-A32132-50ULSize:50 μL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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CAS Number
9007-83-4
Gene Aliases
ARTS, CMTX5, Deafness 2 perceptive congenital, Deafness X linked 2 perceptive congenital, DFN2, DFNX1, EC 2.7.6.1, KIAA0967, Phosphoribosyl pyrophosphate synthase I, Phosphoribosyl pyrophosphate synthetase I, PPRibP, Prps1, PRPS1_HUMAN, PRS I, PRS-I, PRSI, Ribose phosphate pyrophosphokinase I, Ribose-phosphate pyrophosphokinase 1
UniProt
P60891
Host
Rabbit
Antigen Species
Human
Reactivity
Human
Target Antigen
Recombinant Human Ribose-phosphate pyrophosphokinase 1 protein (1-318AA)
Target
PRPS1
Clonality
Polyclonal
Conjugation
Non-conjugated
Applications
ELISA, WB, IHC
Purification Method
Antigen affinity purified
Form
Liquid
Buffer
PBS, 0.02% sodium azide, 50% glycerol, pH 7.3.
Storage Conditions
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Fragment
IgG

UniProtKB · P60891

Ribose-phosphate pyrophosphokinase 1

PRPS1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P60891
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
PRPS1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
2.7.6.1
Processing
—
Secondary accessions
B1ALA8, B2R6T7, B4DNL6, D3DUX6, P09329
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Ligand

ATP-bindingMagnesiumMetal-bindingNucleotide-binding

Disease

Charcot-Marie-Tooth diseaseDeafnessDisease variantGoutIntellectual disabilityNeurodegenerationNeuropathyNon-syndromic deafnessRetinitis pigmentosa

Molecular function

KinaseTransferase

Biological process

Nucleotide biosynthesis

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