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IDS Polyclonal Antibody

CAT: 0763-E-AB-53138-02Size: 60 µLDry Ice: NoHazardous: No
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CAT#:0763-E-AB-53138-02Size:60 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Background
Iduronate 2-sulfatase (IDS) is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations causing IDS deficiency in humans result in the lysosomal storage of these glycosaminoglycans and Hunter syndrome, an X chromosome-linked disease. An internal proteolytic cleavage occurs to produce the mature IDS present in human liver shown to contain a 42 kDa polypeptide N-terminal to a 14 kDa polypeptide..
Abbreviation
IDS
UniProt
P22304
Host
Rabbit
Reactivity
Human; Mouse
Immunogen
Fusion protein of human IDS
Target
Alpha L iduronate sulfate sulfatase; Alpha-L-iduronate sulfate sulfatase; AW214631; Ids; IDS; Iduronate 2 sulfatase 14 kDa chain; Iduronate 2 sulfatase 42 kDa chain; Iduronate 2 sulfatase; Iduronate 2-sulfatase 14 kDa chain; Iduronate sulfatase; Idursulfase; MPS2; RP23-29M4.1; SIDS
Clonality
Polyclonal
Conjugation
Unconjugated
Applications
IHC
Field of Research
Cell Biology
Purification
Antigen affinity purification
Concentration
1.2 mg/mL
Dilution
IHC 1:50-1:200
Buffer
PBS with 0.05% NaN3 and 40% Glycerol, pH7.4
Shipping Conditions
The product is shipped with ice pack, upon receipt, store it immediately at the temperature recommended.
Storage Conditions
Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Isotype
IgG

UniProtKB · P22304

Iduronate 2-sulfatase

IDS_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P22304
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
IDS
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
3.1.6.13
Processing
Precursor
Secondary accessions
D3DWT4, Q14604, Q9BRM3
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Ligand

CalciumMetal-binding

Disease

Disease variantMucopolysaccharidosis

PTM

Disulfide bondGlycoproteinZymogen

Molecular function

Hydrolase

Cellular component

Lysosome

Domain

Signal

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