Mrpl40 Antibodies

AND Mrpl40 ELISA kits, Mrpl40 Proteins

Many biological assays use antibodies to detect Mrpl40, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Mrpl40 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Mrpl40 antibodies...

We validate the specificity of these antibodies to Mrpl40 by testing them on tissues known to express Mrpl40 positively and negatively. Browse below to find the Mrpl40 antibody that suites your experiment. We have 3 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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Mrpl40 Infographic by Boster Bio

All Mrpl40 Products

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Specificity

Applications

Price

Anti-MRP-L40 Antibody

4 Q&As

Western Blot (WB) analysis of specific cells using MRP-L40 Polyclonal antibody

Human, Mouse, Rat

ELISA, IF, IHC, WB

$399
Cat # A11512
100μl

MRPL40 (NM_003776) Human Over-expression Lysate

Human

$628
Cat # LS064976
20 µg, 100 µg

Anti-MRPL40 Antibody

Human

ELISA, IP, IF, IHC, ICC, WB

$370
Cat # A11512-2
100 μl/vial

Mrpl40 Overview

Facts about 39S ribosomal protein L40, mitochondrial.

39S ribosomal protein L40, mitochondrial (Mrpl40)

Gene Information

Mouse
Gene Name:	Mrpl40
Uniprot:	Q9Z2Q5
Entrez:	18100

Family

Belongs to:

mitochondrion-specific ribosomal protein mL40 family

Alternative Names

FLJ41774; L40mt; MGC9400; mitochondrial ribosomal protein L40; MRP-L22,39S ribosomal protein L40, mitochondrial; MRP-L40; NLVCFURIM; nuclear localization signal containing protein deleted in velocardiofacialsyndrome; nuclear localization signal deleted in velocardiofacial syndrome; Nuclear localization signal-containing protein deleted in velocardiofacialsyndrome; Up-regulated in metastasis

Molecular Weight

Mass (kDA):
24.301 kDA

Genomic Context


Mouse

Location:	16 A3\|16 11.69 cM
Sequence:	16;

Tissue Specificity

Ubiquitous.

Diseases

Digeorge Syndrome
Learning Disorders
Learning Disabilities
Craniofacial Abnormalities
Haploinsufficiency
Vascular Ring
Congenital Disorders
Right Aortic Arch (disorder)
Congenital Heart Defects

Aberrant Subclavian Artery
Cytogenetic Abnormality
Retroesophageal Subclavian Artery
Dysequilibrium Syndrome

Pathways

Oxidative Phosphorylation
Localization

PTMs

Phosphorylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/Mrpl40

References

PMID: 9790763 by Funke B., et al. Isolation and characterization of a human gene containing a nuclear localization signal from the critical region for velo-cardio-facial syndrome on 22q11.