MRPS16 Antibody

Code CSB-PA869890
Size US$297
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  • Western blot analysis of extracts from HepG2 cells, using MRPS16 antibody.
  • Immunohistochemistry analysis of paraffin-embedded human tonsil tissue using MRPS16 antibody.
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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) MRPS16 Polyclonal antibody
Uniprot No.
Target Names
MRPS16
Alternative Names
28S ribosomal protein S16 antibody; 28S ribosomal protein S16 mitochondrial antibody; CGI-132 antibody; COXPD2 antibody; mitochondrial antibody; Mitochondrial ribosomal protein S16 antibody; MRP-S16 antibody; mrps16 antibody; RPMS16 antibody; RT16_HUMAN antibody; S16mt antibody
Raised in
Rabbit
Species Reactivity
Human,Mouse
Immunogen
Synthesized peptide derived from internal of Human MRPS16.
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,IHC
Recommended Dilution
Application Recommended Dilution
WB 1:500-1:3000
IHC 1:50-1:100
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. Mutual effect of human ribosomal proteins S5 and S16 on their binding with 18S rRNA fragment 1203-1236/1521-1698 PMID: 19807034
  2. Defective mitochondrial translation caused by a ribosomal protein (MRPS16) mutation. PMID: 15505824
  3. The effect of mutated MRPS16 on the assembly of the small and large ribosomal units in human mitochondria is reported. PMID: 18539099
Involvement in disease
Combined oxidative phosphorylation deficiency 2 (COXPD2)
Subcellular Location
Mitochondrion.
Protein Families
Bacterial ribosomal protein bS16 family
Database Links

HGNC: 14048

OMIM: 609204

KEGG: hsa:51021

STRING: 9606.ENSP00000362036

UniGene: Hs.180312

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