Rabbit polyclonal GNS antibody (A7489)

$69.00$259.00

Reactivity: Human,Mouse,Rat
Applications: WB,IHC
Conjugation: Unconjugated
Supplier: ABclonal Inc.

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Rabbit polyclonal GNS antibody (A7489)

Supplier: ABclonal Inc.

Recommended applications: WB,IHC

Recommended dilution:

WB 1:500 – 1:2000 IHC 1:50 – 1:200

Recommended protocols: check protocols

Image descriptions:

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Alternative names:

Check alternative names for the antibody

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G6S antibody
2610016K11Rik antibody|AU042285 antibody|C87209 antibody|G6S antibody|Glucosamine (N-acetyl) 6 sulfatase antibody|Glucosamine 6 sulfatase antibody|Glucosamine-6-sulfatase antibody|GNS antibody|GNS_HUMAN antibody|MGC21274 antibody|N acetylglucosamine 6 sulfatase [Precursor] antibody|N-acetylglucosamine-6-sulfatase antibody|N28088 antibody|Anti-GNS antibody [EPR8329(2)] (ab154177)

SCBT cat No: sc-161668|sc-161669|

Name

Rabbit polyclonal GNS antibody

Catalogue No.

A7489

Reactivity

Human, Mouse, Rat

Immunogen

Recombinant protein of human GNS

Host

Rabbit

Applications

WB, IHC

Recommended dilution

WB 1:500 – 1:2000
IHC 1:50 – 1:200

Clonality

Polyclonal

Conjugation

Unconjugated

Isotype

IgG

Molecular weight

Predicted: 62kDa/Observed: Refer to figures

Formulation

GNS antibody was tube-contained.
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Purification

GNS antibody was purified using affinity purification.

Storage

Store at -20 Celsius degree. Avoid freeze / thaw cycles.

Alternative antibody names

G6S antibody

Database links

Human UniProt/Swiss-Prot:P15586

Protein names

G6S

Protein sequence and domain

Belongs to the sulfatase family.

Protein post-translational modifications

The form A (78 kDa) is processed by internal peptidase cleavage to a 32 kDa N-terminal species (form B) and a 48 kDa C-terminal species.; The conversion to 3-oxoalanine (also known as C-formylglycine, FGly), of a serine or cysteine residue in prokaryotes and of a cysteine residue in eukaryotes, is critical for catalytic activity.

Protein cellular localization

Lysosome.

Background

The product of this gene is a lysosomal enzyme found in all cells. It is involved in the catabolism of heparin, heparan sulphate, and keratan sulphate. Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome). Mucopolysaccharidosis type IIID is the least common of the four subtypes of Sanfilippo syndrome.

Note

AntibodyPlus can customize GNS antibody according to your requirement, including bulk product size,etc. Please contact info@antibodyplus.com. AntibodyPlus provides antibody trial sample for your own antibody validation.

Product type

Primary antibody

Supplier

ABclonal Inc.

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