PRPS1 (NM_002764) Human Recombinant Protein

Product Name

PRPS1 (NM_002764) Human Recombinant Protein

View all PRPS1 recombinant proteins

SKU/Catalog Number

PROTP60891

Size

20 µg

Tag

C-Myc/DDK

Description

Recombinant protein of human phosphoribosyl pyrophosphate synthetase 1 (PRPS1)

Storage & Handling

Store at -80°C. Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles.

Cite This Product

PRPS1 (NM_002764) Human Recombinant Protein (Boster Biological Technology, Pleasanton CA, USA, Catalog # PROTP60891)

Form

Frozen Solution in PBS Buffer

Formulation

25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol

Concentration

>50 ug/mL as determined by microplate BCA method

Purity

> 80% as determined by SDS-PAGE and Coomassie blue staining

Predicted MW

34.834kDa

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Validation Images & Assay Conditions

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Coomassie blue staining of purified PRPS1 protein. The protein was produced from HEK293T cells transfected with PRPS1 cDNA clone.

Gene/Protein Information For PRPS1 (Source: Uniprot.org, NCBI)

Alternative Names

CMTX5ARTS; deafness, X-linked 2, perceptive, congenital; DFN2; DFNX1KIAA0967; dJ1070B1.2 (phosphoribosyl pyrophosphate synthetase 1); EC 2.7.6.1; Phosphoribosyl pyrophosphate synthase I; phosphoribosyl pyrophosphate synthetase 1; PPRibP; PRSI; PRS-I; ribose-phosphate diphosphokinase 1; ribose-phosphate pyrophosphokinase 1 PRPS1 ARTS, CMTX5, DFN2, DFNX1, PPRibP, PRS-I, PRSI phosphoribosyl pyrophosphate synthetase 1 ribose-phosphate pyrophosphokinase 1|dJ1070B1.2 (phosphoribosyl pyrophosphate synthetase 1)|deafness 2, perceptive, congenital|deafness, X-linked 2, perceptive, congenital|phosphoribosyl pyrophosphate synthase I|ribose-phosphate diphosphokinase 1

For more info on PRPS1, check out the PRPS1 Infographic

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In this infographic, you will see the following information for PRPS1: database IDs, superfamily, protein function, synonyms, molecular weight, chromosomal locations, tissues of expression, subcellular locations, post-translational modifications, and related diseases, research areas & pathways. If you want to see more information included, or would like to contribute to it and be acknowledged, please contact us at [email protected].

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