Mouse Anti-MRPS34 Recombinant Antibody (CBFYM-2584) (CBMAB-M2772-FY)

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Basic Information

Host Animal
Mouse
Clone
CBFYM-2584
Application
WB, IHC, IF
Immunogen
Full length human recombinant protein of human MRPS34(NP_076425) produced in E.coli
Specificity
Human, Dog
Antibody Isotype
IgG1
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
PBS, pH 7.3, 1% BSA
Preservative
0.02% Sodium azide
Concentration
1 mg/mL
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.
More Infomation

Target

Full Name
MITOCHONDRIAL RIBOSOMAL PROTEIN S34
Introduction
Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 28S subunit protein. Alternative splicing results in multiple transcript variants.
Entrez Gene ID
UniProt ID
HumanP82930
DogE2R798
Alternative Names
Mitochondrial Ribosomal Protein S34; Mitochondrial Small Ribosomal Subunit Protein MS34; MRP-S34; S34mt; 28S Ribosomal Protein S34, Mitochondrial; Mitochondrial 28S Ribosomal Protein S34; MRP-S12; COXPD32; MRPS12
Function
Required for mitochondrial translation, plays a role in maintaining the stability of the small ribosomal subunit and the 12S rRNA that are required for mitoribosome formation.
Biological Process
Mitochondrial translation Source: ComplexPortal
Cellular Location
Mitochondrion
Involvement in disease
Combined oxidative phosphorylation deficiency 32 (COXPD32):
An autosomal recessive disorder due to deficiency of mitochondrial respiratory chain complexes, I, III and IV, and characterized by delayed psychomotor development and neurodevelopmental regression. Additional variable symptoms include poor or absent speech, inability to walk, and abnormal movements.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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