MRPL32 Antibodies

AND MRPL32 ELISA kits, MRPL32 Proteins

Many biological assays use antibodies to detect MRPL32, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with MRPL32 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop MRPL32 antibodies...

We validate the specificity of these antibodies to MRPL32 by testing them on tissues known to express MRPL32 positively and negatively. Browse below to find the MRPL32 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.

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MRPL32 Infographic by Boster Bio

All MRPL32 Products

Product

Figures

Specificity

Applications

Price

Anti-MRPL32 Antibody

6 Q&As

Human

IF, WB

$360
Cat # A14134
100 µl

Anti-MRPL32 Antibody

Human, Mouse, Rat

$405
Cat # A14134-1
100ul

Anti-MRP-L32 Antibody

Human

ELISA, IF, IHC, WB

$380
Cat # A14134-2
100ul

MRPL32 (NM_031903) Human Recombinant Protein

$1249
Cat # PROTQ9BYC8
20 µg

MRPL32 (NM_031903) Human Over-expression Lysate

Human

$628
Cat # LS064983
100 µg

MRPL32 Overview

Facts about 39S ribosomal protein L32, mitochondrial.

MRPL32 3D structure. Source: alphafold

39S ribosomal protein L32, mitochondrial (MRPL32)

Gene Information

Human
Gene Name:	MRPL32
Uniprot:	Q9BYC8
Entrez:	64983

Family

Belongs to:

bacterial ribosomal protein bL32 family

Alternative Names

39S ribosomal protein L32, mitochondrial; HSPC283; L32mtMRP-L32bMRP-59b; mitochondrial ribosomal protein L32

Molecular Weight

Mass (kDA):
21.405 kDA

Genomic Context


Human

Location:	7p14.1
Sequence:	7; NC_000007.14 (42932376..42937857)

Subcellular Localizations

Mitochondrion.

Diseases

Paraplegia
Neurodegenerative Disorders
Spastic Paraplegia
Spastic Paraplegia, Hereditary
Aortic Aneurysm, Abdominal

Pathways

Translation
Ribosome Assembly
Ribosome Biogenesis
Cell Death
Mitochondrial Translation

PTMs

Cleavage

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/MRPL32

References

PMID: 11279069 by Suzuki T., et al. Structural compensation for the deficit of rRNA with proteins in the mammalian mitochondrial ribosome. Systematic analysis of protein components of the large ribosomal subunit from mammalian mitochondria.

PMID: 11543634 by Kenmochi N., et al. The human mitochondrial ribosomal protein genes: mapping of 54 genes to the chromosomes and implications for human disorders.