MRPS22 Antibody

Code CSB-PA785563
Size US$297
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  • Western blot analysis of extracts from COS cells, using MRPS22 antibody.
  • Immunofluorescence analysis of A549 cells, using MRPS22 antibody.
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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) MRPS22 Polyclonal antibody
Uniprot No.
Target Names
MRPS22
Alternative Names
28S ribosomal protein S22 antibody; C3orf5 antibody; COXPD5 antibody; GIBT antibody; GK002 antibody; mitochondrial antibody; Mitochondrial ribosomal protein S22 antibody; MRP-S22 antibody; MRPS22 antibody; RPM S22 antibody; RPMS22 antibody; RT22_HUMAN antibody; S22mt antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Synthesized peptide derived from internal of Human MRPS22.
Immunogen Species
Homo sapiens (Human)
Clonality
Polyclonal
Purification Method
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration
It differs from different batches. Please contact us to confirm it.
Form
Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Tested Applications
ELISA,WB,IF
Recommended Dilution
Application Recommended Dilution
WB 1:500-1:3000
IF 1:100-1:500
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Gene References into Functions
  1. hypertrophic cardiomyopathy and tubulopathy may not be considered as constant features of MRPS22 PMID: 28752220
  2. A mutation in the MRPS22 gene led to reduction of 12sRNA in fibroblasts and fatal neonatal hypertrophic cardiomyopathy & kidney tubulopathy. PMID: 17873122
  3. The effect of mutated MRPS22 on the assembly of the small and large ribosomal subunits in human mitochondria is reported. PMID: 18539099
Involvement in disease
Combined oxidative phosphorylation deficiency 5 (COXPD5)
Subcellular Location
Mitochondrion.
Protein Families
Mitochondrion-specific ribosomal protein mS22 family
Database Links

HGNC: 14508

OMIM: 605810

KEGG: hsa:56945

STRING: 9606.ENSP00000310785

UniGene: Hs.745001

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7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA
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