NAGA Antibodies

AND NAGA ELISA kits, NAGA Proteins

Many biological assays use antibodies to detect NAGA, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with NAGA in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop NAGA antibodies...

We validate the specificity of these antibodies to NAGA by testing them on tissues known to express NAGA positively and negatively. Browse below to find the NAGA antibody that suites your experiment. We have 5 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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NAGA Infographic by Boster Bio

All NAGA Products

Product

Figures

Specificity

Applications

Price

Anti-NAGA Antibody

Human, Mouse, Rat

IF, ICC, WB

$405
Cat # A04163
100ul

Human a-N-acetylgalactosaminidase Recombinant Protein

SDS-PAGE

$250
Cat # PROTP17050
Starting from 4ug

Anti-NAGA Mouse Monoclonal Antibody [Clone ID: OTI3A4]

Human

IHC, WB

$523
Cat # M04163
100 µl

NAGA (NM_000262) Human Over-expression Lysate

Human

$628
Cat # LS004668
100 µg

Human NAGA ELISA Kit PicoKine®

Human

ELISA

$750
Cat # EK2248
96 wells/kit, with removable strips.

NAGA Overview

Facts about Alpha-N-acetylgalactosaminidase.

NAGA 3D structure. Source: alphafold

Alpha-N-acetylgalactosaminidase (NAGA)

Removes terminal alpha-N-acetylgalactosamine residues from glycolipids and glycopeptides. Required for the breakdown of glycolipids.

Gene Information

Human
Gene Name:	NAGA
Uniprot:	P17050
Entrez:	4668

Family

Belongs to:

glycosyl hydrolase 27 family

Alternative Names

alpha-N- (alpha-galactosidase B); alphaNacetylgalactosaminidase; alpha-N-acetylgalactosaminidase; EC 3.2.1; EC 3.2.1.49; GALB; N-acetylgalactosaminidase, alpha-; NAGA

Molecular Weight

Mass (kDA):
46.565 kDA

Genomic Context


Human

Location:	22q13.2
Sequence:	22; NC_000022.11 (42058334..42070842, complement)

Subcellular Localizations

Lysosome.

Diseases

Alpha-n-acetylgalactosaminidase Deficiency
Lysosomal Storage Diseases
Dystrophy
Fabry Disease
Neuroaxonal Dystrophies
Angiokeratoma
Kidney Diseases
Malignant Neoplasms
Carcinoma
Neoplasms
Infantile Neuroaxonal Dystrophy

Infective Disorder
Diabetes Mellitus
Storage Disease
Ischemia
Albinism
Trematode Infections

Pathways

Excretion
Transport
Secretion
Glycosylation
Pathogenesis
Virulence
Glycolysis
Fermentation
Reverse Transcription
Phagocytosis
Sulfation
Autolysis
Localization

Glomerular Filtration
Macrophage Activation
N-acetylglucosamine Transport
Cell Death
Protein Phosphorylation
Constitutive Secretory Pathway
Protein Maturation

PTMs

Cleavage
Phosphorylation
Glycosylation
Deglycosylation

Reduction
Deacetylation
Oxidation
Gpi Anchoring

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/NAGA

References

PMID: 2174888 by Wang A.M., et al. Human alpha-N-acetylgalactosaminidase-molecular cloning, nucleotide sequence, and expression of a full-length cDNA. Homology with human alpha-galactosidase A suggests evolution from a common ancestral gene.

PMID: 1646157 by Wang A.M., et al. Structural organization and complete sequence of the human alpha-N- acetylgalactosaminidase gene: homology with the alpha-galactosidase A gene provides evidence for evolution from a common ancestral gene.