MAB21L1 Antibodies

AND MAB21L1 ELISA kits, MAB21L1 Proteins

Many biological assays use antibodies to detect MAB21L1, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with MAB21L1 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop MAB21L1 antibodies...

We validate the specificity of these antibodies to MAB21L1 by testing them on tissues known to express MAB21L1 positively and negatively. Browse below to find the MAB21L1 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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MAB21L1 Infographic by Boster Bio

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MAB21L1 (NM_005584) Human Over-expression Lysate

Human

$628
Cat # LS004081
20 µg, 100 µg

MAB21L1 Overview

Facts about Putative nucleotidyltransferase MAB21L1.

MAB21L1 3D structure. Source: alphafold

Putative nucleotidyltransferase MAB21L1 (MAB21L1)

Putative nucleotidyltransferase required for several aspects of embryonic development including normal evolution of the eye (By similarity). It's unclear whether it displays nucleotidyltransferase activity in vivo (PubMed:27271801).

Binds single-stranded RNA (ssRNA) (PubMed:27271801). .

Gene Information

Human
Gene Name:	MAB21L1
Uniprot:	Q13394
Entrez:	4081

Family

Belongs to:

mab-21 family

Alternative Names

CAGR1mab-21 (C. elegans)-like 1; FLJ10197; mab-21-like 1 (C. elegans); mab-21-like protein 1; protein mab-21-like 1

Molecular Weight

Mass (kDA):
40.956 kDA

Genomic Context


Human

Location:	13q13.3
Sequence:	13; NC_000013.11 (35473789..35476689, complement)

Tissue Specificity

Expressed in brain, cerebellum and skeletal muscle.

Subcellular Localizations

Nucleus.

Diseases

Mood Disorders
Ataxia
Bipolar Disorder
Schizophrenia
Autistic Disorder
Microphthalmos
Malnutrition
Overlying Behavior
Trinucleotide Repeat Expansion
Dementia
Secondary Parkinson Disease
Chimera Disorder

Cytogenetic Abnormality
Myotonic Dystrophy
Embryonic Mosaic
Aphakia
Chromosomal Deletion
Hearing Problem

Interacting Proteins

SIAH1

Pathways

Osteoblast Differentiation
Tube Development
Eye Morphogenesis
Cell Proliferation
Cell Death
Brain Development
Bone Development
Neural Tube Development
Vasculogenesis

Eye Development
Bone Resorption
Localization

PTMs

Phosphorylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/MAB21L1

References

PMID: 8733127 by Margolis R.L., et al. cDNA cloning of a human homologue of the Caenorhabditis elegans cell fate-determining gene mab-21: expression, chromosomal localization and analysis of a highly polymorphic (CAG)n trinucleotide repeat.

PMID: 12880961 by Ohira M., et al. Neuroblastoma oligo-capping cDNA project: toward the understanding of the genesis and biology of neuroblastoma.