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NXNL1 Antibodies

AND NXNL1 ELISA kits, NXNL1 Proteins

Many biological assays use antibodies to detect NXNL1, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with NXNL1 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop NXNL1 antibodies...

We validate the specificity of these antibodies to NXNL1 by testing them on tissues known to express NXNL1 positively and negatively. Browse below to find the NXNL1 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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NXNL1 Infographic by Boster Bio

NXNL1 protein infographic

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TXNL6 (NXNL1) (NM_138454) Human Over-expression Lysate

TXNL6 (NXNL1) Human Over-expression Lysates NM_138454

TXNL6 (NXNL1) Human Over-expression Lysates NM_138454

Human

$628
Cat # LS115861
20 µg, 100 µg

NXNL1 Overview

Facts about Nucleoredoxin-like protein 1.

NXNL1 3D structure

NXNL1 3D structure. Source: alphafold

Nucleoredoxin-like protein 1 (NXNL1)

May play a role in cone cell viability, slowing down cone degeneration, does not seem to play a role in degenerating rods. .

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Gene Information

Human
Gene Name:	NXNL1
Uniprot:	Q96CM4
Entrez:	115861

Gene Information

Family

Belongs to:

nucleoredoxin family

Family

Alternative Names

nucleoredoxin-like 1; nucleoredoxin-like protein 1; RDCVF; rod-derived cone viability factor; thioredoxin-like 6; Thioredoxin-like protein 6; TXNL6

Molecular Weight

Mass (kDA):
23.943 kDA

Molecular Weight

Genomic Context


Human

Location:	19p13.11
Sequence:	19; NC_000019.10 (17455425..17460926, complement)

Subcellular Localizations

Cell projection, cilium, photoreceptor outer segment.

Subcellular Localization

Diseases

Retinitis Pigmentosa
Retinal Degeneration
Blind Vision
Retinal Diseases
Amaurosis
Congenital Abnormality
Neurodegenerative Disorders
Bardet-biedl Syndrome
Age Related Macular Degeneration
Cataract

Leber Congenital Amaurosis
Disorder Of Eye
Eye Diseases, Hereditary
Alzheimer's Disease
Optic Atrophy, Hereditary, Leber

Disease

Pathways

Cell Death
Programmed Cell Death
Aging

Pathways

PTMs

Phosphorylation

Bosterbio | ELISA Kits, Antibodies, Antibody Company

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/NXNL1

References

PMID: 17286855 by Roni V., et al. Mapping of transcription start sites of human retina expressed genes.