NAALADL2 Antibodies

AND NAALADL2 ELISA kits, NAALADL2 Proteins

Many biological assays use antibodies to detect NAALADL2, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with NAALADL2 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop NAALADL2 antibodies...

We validate the specificity of these antibodies to NAALADL2 by testing them on tissues known to express NAALADL2 positively and negatively. Browse below to find the NAALADL2 antibody that suites your experiment. We have 1 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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NAALADL2 Infographic by Boster Bio

All NAALADL2 Products

Product

Figures

Specificity

Applications

Price

Anti-NADL2 NAALADL2 Antibody

Human

ELISA, WB

$380
Cat # A11421
100ul

NAALADL2 Overview

Facts about Inactive N-acetylated-alpha-linked acidic dipeptidase-like protein 2.

NAALADL2 3D structure. Source: alphafold

Inactive N-acetylated-alpha-linked acidic dipeptidase-like protein 2 (NAALADL2)

May be catalytically inactive. .

Gene Information

Human
Gene Name:	NAALADL2
Uniprot:	Q58DX5
Entrez:	254827

Family

Belongs to:

peptidase M28 family

Alternative Names

inactive N-acetylated-alpha-linked acidic dipeptidase-like protein 2; NAALADase L2; NAALADase like 2; NAALADase-like 2; NAALADL2; N-acetylated alpha-linked acidic dipeptidase 2; N-acetylated alpha-linked acidic dipeptidase-like 2

Molecular Weight

Mass (kDA):
88.682 kDA

Genomic Context


Human

Location:	3q26.31
Sequence:	3; NC_000003.12 (174438534..175810548)

Tissue Specificity

Expressed at higher level in kidney and placenta. In embryo, it is mainly confined to duodenal and stomach endoderm, mesonephros, metanephros and pancreas.

Subcellular Localizations

Membrane; Single-pass type II membrane protein.

Diseases

Congenital Abnormality
Cornelia De Lange Syndrome
Mild Mental Retardation
Communicable Diseases
Growth Retardation
Cardiovascular Diseases
Mucocutaneous Lymph Node Syndrome
Obesity
Chromosome Breakage

Inflammation
Cytogenetic Abnormality
Vasculitis

Interacting Proteins

GPR25
GRM2
ITM2B
LAPTM4B
SLC30A3

Pathways

Pathogenesis

PTMs

Acetylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/NAALADL2

References

PMID: 15168106 by Tonkin E.T., et al. A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3.