IDS Polyclonal Antibody | G-AB-04629

IDS Polyclonal Antibody | G-AB-04629 | Gentaur Antibodies

Overview: 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..

Category Type: Polyclonal Antibody

Research Areas: Cell Biology

Synonyms: 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

Reactivity: Human, Mouse

Host: Rabbit

Isotype: IgG

Gene ID:

Accession #: BC006170

Clonality: Polyclonal

Immunogen: Fusion protein of human IDS

Clone #:

Conjugation: Unconjugated

Swissprot: P22304

Santa Cruz:

Calculated MW:

Observed MW:

Concentration: 1.02 mg/mL

Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

Purification method: Antigen affinity purification

Application: IHC, ELISA

Dilution: IHC 1:50-1:200, ELISA 1:5000-1:10000

Storage: Store at -20°C. Avoid freeze / thaw cycles.

IDS Polyclonal Antibody DataSheet