MRPS22 Antibodies

AND MRPS22 ELISA kits, MRPS22 Proteins

Many biological assays use antibodies to detect MRPS22, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with MRPS22 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop MRPS22 antibodies...

We validate the specificity of these antibodies to MRPS22 by testing them on tissues known to express MRPS22 positively and negatively. Browse below to find the MRPS22 antibody that suites your experiment. We have 5 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.

Previous: Septin9 Next: EMSY

MRPS22 Infographic by Boster Bio

All MRPS22 Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

Anti-MRPS22 Antibody

5 Q&As

Human

IF, WB

$360
Cat # A10300
100 µl

Anti-MRP-S22 (R263) Antibody

Human

IF, IHC

$405
Cat # A10300S22
100ul

Anti-MRPS22 Antibody

Human, Mouse, Rat

$405
Cat # A10300-1
100ul

Anti-MRP-S22 Antibody

Human, Monkey

ELISA, IF, IHC, WB

$380
Cat # A10300S22-1
100ul

Anti-MRPS22 Antibody Picoband®

Human

ELISA, Flow Cytometry, IF, IHC, ICC, WB

$370
Cat # A10300-2
100 μg/vial

MRPS22 Overview

Facts about 28S ribosomal protein S22, mitochondrial.

MRPS22 3D structure. Source: alphafold

28S ribosomal protein S22, mitochondrial (MRPS22)

Gene Information

Human
Gene Name:	MRPS22
Uniprot:	P82650
Entrez:	56945

Family

Belongs to:

mitochondrion-specific ribosomal protein mS22 family

Alternative Names

C3orf5GK002; COXPD5; GIBT; mitochondrial ribosomal protein S22; MRP-S2228S ribosomal protein S22, mitochondrial; RPMS22; S22mt

Molecular Weight

Mass (kDA):
41.28 kDA

Genomic Context


Human

Location:	3q23
Sequence:	3; NC_000003.12 (139343994..139357140)

Subcellular Localizations

Mitochondrion.

Diseases

Hypertrophic Cardiomyopathy
Cardiomyopathies
Microcephaly
Premature Menopause
Fetal Diseases
Mitochondrial Diseases
Cornelia De Lange Syndrome
Infertility
Muscle Hypotonia
Mitochondrial Myopathies
Female Infertility
Ovarian Failure, Premature

Skin Oedema
Hypertensive Disease
Edema
Obesity
Hypertrophy
Chromosome Breakage
Chromosomal Translocation

Pathways

Translation
Mitochondrial Translation
Oxidative Phosphorylation

PTMs

Acetylation

Phosphoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/MRPS22

References

PMID: 11175783 by Crisponi L., et al. The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome.

PMID: 10938081 by Koc E.C., et al. A proteomics approach to the identification of mammalian mitochondrial small subunit ribosomal proteins.