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NAP1L2 Antibodies

AND NAP1L2 ELISA kits, NAP1L2 Proteins

Many biological assays use antibodies to detect NAP1L2, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with NAP1L2 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop NAP1L2 antibodies...

We validate the specificity of these antibodies to NAP1L2 by testing them on tissues known to express NAP1L2 positively and negatively. Browse below to find the NAP1L2 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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NAP1L2 Infographic by Boster Bio

NAP1L2 protein infographic

All NAP1L2 Products

Product

Figures

Specificity

Applications

Price

NAP1L2 (NM_021963) Human Over-expression Lysate

Human

$628
Cat # LS004674
100 µg

NAP1L2 Overview

Facts about Nucleosome assembly protein 1-like 2.

NAP1L2 3D structure

NAP1L2 3D structure. Source: alphafold

Nucleosome assembly protein 1-like 2 (NAP1L2)

Acidic protein which might be involved in interactions with other proteins or DNA. .

.

Gene Information

Human
Gene Name:	NAP1L2
Uniprot:	Q9ULW6
Entrez:	4674

Gene Information

Family

Belongs to:

nucleosome assembly protein (NAP) family

Family

Alternative Names

BPXMGC26243; brain specific gene BPX; Brain-specific protein, X-linked; nucleosome assembly protein 1-like 2

Molecular Weight

Mass (kDA):
52.542 kDA

Molecular Weight

Genomic Context


Human

Location:	Xq13.2
Sequence:	X; NC_000023.11 (73212299..73214851, complement)

Subcellular Localizations

Nucleus.

Subcellular Localization

Diseases

Anencephaly
Spina Bifida
Isodicentric Chromosome
Sex Chromosome Aberrations
Leukemia, Myelocytic, Acute
Myeloid Leukemia
Nervousness
Leukemia
Chromosome Breakage

Chimera Disorder
Cytogenetic Abnormality
Dysmyelopoietic Syndromes
Preleukemia

Disease

Pathways

Nucleosome Assembly
Histone Acetylation
Cell Proliferation
G1 Phase
Dna Methylation
Neurogenesis
Metaphase
Localization
Lateral Inhibition
Demethylation

Methylation
Cell Cycle
S Phase
Chromatin Modification

Pathways

PTMs

Acetylation

Demethylation

Methylation

Research Areas

Stem Cell Markers

Research Areas

Bosterbio | ELISA Kits, Antibodies, Antibody Company

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/NAP1L2

References

PMID: 14702039 by Ota T., et al. Complete sequencing and characterization of 21,243 full-length human cDNAs.

PMID: 15772651 by Ross M.T., et al. The DNA sequence of the human X chromosome.