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CoraLite® Plus 488-conjugated IDS Recombinant monoclonal antibody

IDS Uni-rAb® Recombinant Antibody for IF/ICC

Cat No. CL488-84623-7
Clone No.242054G12

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

IF/ICC

242054G12, Alpha-L-iduronate sulfate sulfatase, EC:3.1.6.13, Iduronate 2-sulfatase, Iduronate 2-sulfatase 14 kDa chain

Formulation:  PBS, Proclin300, BSA, Glycerol
PBS, Proclin300, BSA, Glycerol
Conjugate:  CoraLite® Plus 488
Size/Concentration: 
SKU: 

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Quantity

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Tested Applications

Positive IF/ICC detected inHeLa cells

Recommended dilution

ApplicationDilution
Immunofluorescence (IF)/ICCIF/ICC : 1:500-1:2000
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

CL488-84623-7 targets IDS in IF/ICC applications and shows reactivity with human samples.

Tested Reactivity human
Host / Isotype Rabbit / IgG
Class Recombinant
Type Antibody
Immunogen

CatNo: Ag31132

Product name: Recombinant human IDS protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 160-312 aa of BC006170

Sequence: PSSEKYENTKTCRGPDGELHANLLCPVDVLDVPEGTLPDKQSTEQAIQLLEKMKTSASPFFLAVGYHKPHIPFRYPKEFQKLYPLENITLAPDPEVPDGLPPVAYNPWMDIRQREDVQALNISVPYGPIPVDFQEDQSSTGFRLKTSSTRKYK

Predict reactive species
Full Name iduronate 2-sulfatase
Calculated Molecular Weight312aa,35 kDa; 550aa,62 kDa
GenBank Accession NumberBC006170
Gene Symbol IDS
Gene ID (NCBI) 3423
Conjugate CoraLite® Plus 488 Fluorescent Dye
Excitation/Emission Maxima Wavelengths493 nm / 522 nm
Excitation LaserBlue laser (488 nm)
FormLiquid
Purification MethodProtein A purification
UNIPROT IDP22304
Storage Buffer PBS with 50% glycerol, 0.05% Proclin300, 0.5% BSA, pH 7.3.
Storage ConditionsStore at -20°C. Avoid exposure to light. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

Background Information

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. IDS is synthesized as two precursor forms of 76 and 90 kDa that are converted, through a 62 kDa intermediate, to mature polypeptides due to an internal proteolytic cleavage (PMID: 10838181).

Protocols

Product Specific Protocols
IF protocol for CL Plus 488 IDS antibody CL488-84623-7Download protocol
Standard Protocols
Click here to view our Standard Protocols
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