EPB42 Antibodies

AND EPB42 ELISA kits, EPB42 Proteins

Many biological assays use antibodies to detect EPB42, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with EPB42 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop EPB42 antibodies...

We validate the specificity of these antibodies to EPB42 by testing them on tissues known to express EPB42 positively and negatively. Browse below to find the EPB42 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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EPB42 Infographic by Boster Bio

All EPB42 Products

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Anti-EPB42 Antibody Picoband®

Western blot analysis of EPB42 using anti-EPB42 antibody (A08148-1)

Human, Rat

ELISA, WB

$370
Cat # A08148-1
100 μg/vial

EPB42 Overview

Facts about Erythrocyte membrane protein band 4.2.

EPB42 3D structure. Source: alphafold

Erythrocyte membrane protein band 4.2 (EPB42)

Probably plays a significant role in the regulation of erythrocyte shape and mechanical properties. .

Gene Information

Human
Gene Name:	EPB42
Uniprot:	P16452
Entrez:	2038

Family

Belongs to:

transglutaminase superfamily

Alternative Names

E42P; erythrocyte membrane protein band 4.2; Erythrocyte protein 4.2; erythrocyte surface protein band 4.2; MGC116735; MGC116737; P4.2; PA; SPH5

Molecular Weight

Mass (kDA):
77.009 kDA

Genomic Context


Human

Location:	15q15.2
Sequence:	15; NC_000015.10 (43197227..43225856, complement)

Subcellular Localizations

Cell membrane; Lipid-anchor; Cytoplasmic side. Cytoplasm, cytoskeleton. Cytoplasmic surface of erythrocyte membranes.

Diseases

Hereditary Spherocytosis
Hydrops Fetalis
Hereditary Diseases
Anemia
Dehydration
Edema
Anemia, Hemolytic, Congenital
Elliptocytosis, Hereditary
Hereditary Stomatocytosis
Stomatocytic Anemia
Pseudohyperkalaemia
Mutation Abnormality

Acidosis
Thalassemia
Channelopathies
Renal Tubular Acidosis
Precursor T-cell Lymphoblastic Leukemia-lymphoma
Acute Lymphocytic Leukemia
Xerocytosis

Interacting Proteins

SPINK7

Pathways

Cell Development
Glycosylation
Pathogenesis
Conjugation

PTMs

Phosphorylation

Glycosylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/EPB42

References

PMID: 2052563 by Korsgren C., et al. Organization of the gene for human erythrocyte membrane protein 4.2: structural similarities with the gene for the a subunit of factor XIII.

PMID: 2300550 by Korsgren C., et al. Complete amino acid sequence and homologies of human erythrocyte membrane protein band 4.2.