MRPS22 polyclonal, anti-human, mouse
€388.00
In stock
SKU
BS72390
Background:
The mitoribosomes are composed of a 4:1 ratio of protein to RNA, with the proteins forming two subunits, the 28S subunit and the 39S subunit. Across species, the proteins that make up the mitoribosome subunits vary greatly in sequence, preventing easy recognition by sequence homology. MRP-S22 (mitochondrial 28S ribosomal protein S22), also known as S22mt, is a 360 amino acid mitochondrial ribosomal protein. Localized to the mitochondria, MRP-S22 is present in the 28S subunit of the mitoribosomes. Defects of MRP-S22 are the cause of combined oxidative phosphorylation deficiency type 5 (COXPD5). COXPD5 is an antenatal mitochondrial disease characterized by hypotonia, edema, cardiomyopathy and tubulopathy.
Alternative Name:
28S ribosomal protein S22, mitochondrial, MRP-S22, S22mt, MRPS22, C3orf5, RPMS22, ORF Names: GK002
Application Dilution: WB: 1:500 - 1:2000, IHC: 1:50 - 1:100
Specificity: MRPS22 polyclonal antibody detects endogenous levels of MRPS22 protein.
Immunogen:
Recombinant protein of human MRPS22
MW: ~ 41 kDa
Swis Prot.: P82650
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1 mg/ml in Phosphate buffered saline (PBS) with 0.05% sodium azide, approx. pH 7.2.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
The mitoribosomes are composed of a 4:1 ratio of protein to RNA, with the proteins forming two subunits, the 28S subunit and the 39S subunit. Across species, the proteins that make up the mitoribosome subunits vary greatly in sequence, preventing easy recognition by sequence homology. MRP-S22 (mitochondrial 28S ribosomal protein S22), also known as S22mt, is a 360 amino acid mitochondrial ribosomal protein. Localized to the mitochondria, MRP-S22 is present in the 28S subunit of the mitoribosomes. Defects of MRP-S22 are the cause of combined oxidative phosphorylation deficiency type 5 (COXPD5). COXPD5 is an antenatal mitochondrial disease characterized by hypotonia, edema, cardiomyopathy and tubulopathy.
Alternative Name:
28S ribosomal protein S22, mitochondrial, MRP-S22, S22mt, MRPS22, C3orf5, RPMS22, ORF Names: GK002
Application Dilution: WB: 1:500 - 1:2000, IHC: 1:50 - 1:100
Specificity: MRPS22 polyclonal antibody detects endogenous levels of MRPS22 protein.
Immunogen:
Recombinant protein of human MRPS22
MW: ~ 41 kDa
Swis Prot.: P82650
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1 mg/ml in Phosphate buffered saline (PBS) with 0.05% sodium azide, approx. pH 7.2.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
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