MRPL3 Antibody

Code CSB-PA003294
Size US$100
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  • Western Blot analysis of Jurkat cells using MRP-L3 Polyclonal Antibody
  • Western Blot analysis of Jurkat cells using MRP-L3 Polyclonal Antibody
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Product Details

Uniprot No.
Target Names
MRPL3
Alternative Names
39S ribosomal protein L3 antibody; 39S ribosomal protein L3 mitochondrial antibody; COXPD9 antibody; L3mt antibody; Mitochondrial 39S ribosomal protein L3 antibody; Mitochondrial 60S ribosomal protein L3 antibody; mitochondrial antibody; mitochondrial ribosomal protein antibody; Mitochondrial ribosomal protein L3 antibody; MRL3 antibody; MRP-L3 antibody; MRPL3 antibody; RM03_HUMAN antibody; RPML3 antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Synthesized peptide derived from the Internal region of Human MRP-L3.
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Isotype
IgG
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.
Buffer
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Form
Liquid
Tested Applications
WB, ELISA
Recommended Dilution
Application Recommended Dilution
WB 1:500-1:2000
ELISA 1:5000
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. Found MRPL3 S75N variant is probably a rare cause of Tourette syndrome/chronic tic phenotype in Chinese Han patients. PMID: 22507240
  2. the first mutation in large mitochondrial ribosomal protein MRPL3 in a family of four sibs with hypertrophic cardiomyopathy, psychomotor retardation, and multiple respiratory chain deficiency.(MRPL3) PMID: 21786366
Involvement in disease
Combined oxidative phosphorylation deficiency 9 (COXPD9)
Subcellular Location
Mitochondrion.
Protein Families
Universal ribosomal protein uL3 family
Database Links

HGNC: 10379

OMIM: 607118

KEGG: hsa:11222

STRING: 9606.ENSP00000264995

UniGene: Hs.205163

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301-363-4651 (Available 9 a.m. to 5 p.m. CST from Monday to Friday)
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Address
7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA
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