IDS ELISA Kit
Quick Overview for IDS ELISA Kit (ABIN6720131)
Target
See all IDS ELISA KitsReactivity
Detection Method
Method Type
Detection Range
Application
Sample Type
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Minimum Detection Limit
- 156 pg/mL
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Supplier Product No.
- koa0877
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Supplier
- Rockland
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Purpose
- Mouse IDS Sandwich ELISA Kit for Quantitative Detection
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Brand
- AccuSignal™
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Analytical Method
- Quantitative
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Specificity
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Production: Natural and recombinant mouse IDS. There is no detectable cross-reactivity with other relevant proteins.
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Sensitivity
- < 15 pg/mL
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Components
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- Antibody-coated 96-well plate
- Target Protein Standard
- Detection antibody
- Detection reagent
- Diluent buffers
- Wash buffers
- Substrate Solution
- Stop solutions
- Adhesive covers
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Application Notes
- Useful in Sandwich ELISA for Quantitative Detection of Antigen. Aliquot 0.1 mL per well of the 10000pg/mL, 5000pg/mL, 2500pg/mL, 1250pg/mL, 625pg/mL, 312pg/mL, 156pg/mL mouse IDS standard solutions into the precoated 96-well plate. Add 0.1 mL of the sample diluent buffer into the control well (Zero well). Add 0.1 mL of each properly diluted sample of mouse cell culture supernates, serum or plasma(heparin, EDTA) to each empty well. It is recommended that each mouse IDS standard solution and each sample be measured in duplicate.
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Comment
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Standard: Expression system for standard: NSO, Immunogen sequence: T36-P552
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Sample Volume
- 100 μL
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Plate
- Pre-coated
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Restrictions
- For Research Use only
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Storage
- 4 °C,-20 °C
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Storage Comment
- Store vials at 4°C prior to opening. Centrifuge product if not completely clear after standing at room temperature. This product is stable for 6 months at 4°C as an undiluted liquid. Dilute only prior to immediate use. For extended storage freeze at -20°C or below for 12 months. Avoid cycles of freezing and thawing.
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Expiry Date
- 12 months
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- IDS (Iduronate 2-Sulfatase (IDS))
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Alternative Name
- IDS
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Background
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Synonyms: Ids, Iduronate 2 sulfatase, Iduronate sulfatase, Idursulfase, MPS2, SIDS
Background: Iduronate 2-sulfatase (IDS) is a sulfatase enzyme associated with Hunter syndrome. It encodes a member of the sulfatase family of proteins. Iduronate 2-sulfatase is involved in the lysosomal degradation of the glycosaminoglycans heparan sulfate and dermatan sulfate. The encoded preproprotein is proteolytically processed to generate two polypeptide chains. Mutations in this gene are associated with the X-linked lysosomal storage disease mucopolysaccharidosis type II, also known as Hunter syndrome. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed.
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Gene ID
- 15931
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NCBI Accession
- NP_034628
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UniProt
- Q08890
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Pathways
- Glycosaminoglycan Metabolic Process
Target See all IDS ELISA Kits
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