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PRPS1 antibody (AA 1-318)
PRPS1
Reactivity: Human
WB, ELISA, IF, ICC
Host: Mouse
Monoclonal
AT1E11
unconjugated
Product Details anti-PRPS1 Antibody
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Target
See all PRPS1 Antibodies
PRPS1
(phosphoribosyl Pyrophosphate Synthetase 1 (PRPS1))
Binding Specificity
All epitopes for PRPS1 antibodies
AA 1-318
Reactivity
All reactivities for PRPS1 antibodies
Human
Host
All hosts for PRPS1 antibodies
Mouse
Clonality
All clonalities for PRPS1 antibodies
Monoclonal
Conjugate
All conjugates for PRPS1 antibodies
This PRPS1 antibody is un-conjugated
Application
All applications for PRPS1 antibodies
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunocytochemistry (ICC)
Purpose
Human PRPS1 antibody
Purification
protein-A affinity chromatography
Immunogen
Recombinant human PRPS1 (1-318aa) purified from E. coli
Clone
AT1E11
Isotype
IgG2a kappa
Top Product
Discover our top product PRPS1 Primary Antibody
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Application Details
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Application Notes
Optimal working dilution should be determined by the investigator.
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
1 mg/mL
Buffer
Phosphate-Buffered Saline (pH 7.4) with 0.02% Sodium Azide, 10% glycero
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
4 °C,-20 °C,-80 °C
Storage Comment
Can be stored at +2°C to +8°C for 1 week. For long term storage, aliquot and store at -20°C to -80°C. Avoid repeated freezing and thawing cycles.
Target Details for PRPS1
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Target
PRPS1
(phosphoribosyl Pyrophosphate Synthetase 1 (PRPS1))
Alternative Name
PRPS1 (PRPS1 Products )
Background
PRPS1 is an enzyme that catalyzes the phosphoribosylation of ribose 5-phosphate to 5-phosphoribosyl-1-pyrophosphate, which is necessary for purine metabolism and nucleotide biosynthesis. A mutation in PRPS1 may result in PRPS superactivity, a disease characterized by gout and the overproductionof purine nucleotides, uric acid and PRPP. PRPS1 mutations can also lead to a reduction in PRPS1 activity resulting in ARTS syndrome or CMTX5 (Charcot-Marie-Tooth disease X-linked recessive type 5).
NCBI Accession
NP_002755
Pathways
Ribonucleoside Biosynthetic Process
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