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Typical Testing Data/Standard Curve (for reference only)

Human SPR (Sepiapterin reductase) ELISA Kit | SPR elisa kit

Human SPR (Sepiapterin reductase) ELISA Kit

Gene Names
SPR; SDR38C1
Reactivity
Human
Synonyms
SPR (Sepiapterin reductase); Human SPR (Sepiapterin reductase) ELISA Kit; Sepiapterin reductase; SPR; SPR elisa kit
Ordering
For Research Use Only!
Reactivity
Human
Assay Type
Sandwich ELISA, Double Antibody
Samples
serum, plasma, tissue homogenates and other biological fluids.
Detection Range
0.156-10ng/ml
Sensitivity
0.094ng/ml
Precision
Intra-Assay: CV<8%
Inter-Assay: CV<10%
Preparation and Storage
Store at 2-8 degree C for 6 months

Typical Testing Data/Standard Curve (for reference only)

Typical Testing Data/Standard Curve (for reference only)

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Accession #
Molecular Weight
28,048 Da
NCBI Official Full Name
sepiapterin reductase
NCBI Official Synonym Full Names
sepiapterin reductase (7,8-dihydrobiopterin:NADP+ oxidoreductase)
NCBI Official Symbol
SPR
NCBI Official Synonym Symbols
SDR38C1
NCBI Protein Information
sepiapterin reductase; short chain dehydrogenase/reductase family 38C, member 1
UniProt Protein Name
Sepiapterin reductase
Protein Family
UniProt Gene Name
SPR
UniProt Synonym Gene Names
SPR
UniProt Entry Name
SPRE_HUMAN

NCBI Description

This gene encodes an aldo-keto reductase that catalyzes the NADPH-dependent reduction of pteridine derivatives and is important in the biosynthesis of tetrahydrobiopterin (BH4). Mutations in this gene result in DOPA-responsive dystonia due to sepiaterin reductase deficiency. A pseudogene has been identified on chromosome 1. [provided by RefSeq, Jul 2008]

Uniprot Description

SPR: Catalyzes the final one or two reductions in tetra- hydrobiopterin biosynthesis to form 5,6,7,8-tetrahydrobiopterin. Defects in SPR are the cause of dystonia DOPA-responsive due to sepiapterin reductase deficiency (DRDSPRD). In the majority of cases, patients manifest progressive psychomotor retardation, dystonia and spasticity. Cognitive anomalies are also often present. The disease is due to severe dopamine and serotonin deficiencies in the central nervous system caused by a defect in BH4 synthesis. Dystonia is defined by the presence of sustained involuntary muscle contractions, often leading to abnormal postures. Belongs to the sepiapterin reductase family.

Protein type: Cofactor and Vitamin Metabolism - folate biosynthesis; EC 1.1.1.153; Oxidoreductase

Chromosomal Location of Human Ortholog: 2p14-p12

Cellular Component: nucleoplasm; mitochondrion; cytoplasm; cytosol

Molecular Function: aldo-keto reductase activity; sepiapterin reductase activity; NADP binding

Biological Process: L-phenylalanine metabolic process; tetrahydrobiopterin biosynthetic process; voluntary musculoskeletal movement; death; pteridine metabolic process; neuron morphogenesis during differentiation; regulation of multicellular organism growth; regulation of nitric-oxide synthase activity; nitric oxide biosynthetic process; norepinephrine metabolic process; dopamine metabolic process; nitric oxide metabolic process; serotonin metabolic process

Disease: Dystonia, Dopa-responsive, Due To Sepiapterin Reductase Deficiency

Research Articles on SPR

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Product Notes

The Human SPR spr (Catalog #AAA7612665) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA7612665 ELISA Kit recognizes Human SPR. It is sometimes possible for the material contained within the vial of "SPR (Sepiapterin reductase), ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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