| Weight | 1 lbs | 
|---|---|
| Dimensions | 9 × 5 × 2 in | 
| host | mouse  | 
		
| isotype | IgG  | 
		
| clonality | monoclonal  | 
		
| concentration | concentrate, predilute  | 
		
| applications | IHC  | 
		
| reactivity | human  | 
		
| available size | 0.1 mL, 0.5 mL, 1 mL concentrated, 7 mL prediluted  | 
		
rabbit anti-RRM1 monoclonal antibody (ZR114) 6356
Price range: $160.00 through $528.00
Antibody summary
- Rabbit monoclonal to RRM1
 - Suitable for: Immunohistochemistry (formalin-fixed, paraffin-embedded tissues)
 - Reacts with: Human
 - Isotype:IgG
 - Control: Breast or colon carcinoma
 - Visualization: cytoplasm
 - 0.1, 0.5, 1.0 mL concentrated, 7 mL prediluted
 
rabbit anti-RRM1 monoclonal antibody ZR114 6356
| target relevance | 
|---|
| Protein names Ribonucleoside-diphosphate reductase large subunit (EC 1.17.4.1) (Ribonucleoside-diphosphate reductase subunit M1) (Ribonucleotide reductase large subunit)  | 
| Gene names RRM1,RRM1 RR1  | 
| Protein family Ribonucleoside diphosphate reductase large chain family  | 
| Mass 90070Da  | 
| Function FUNCTION: Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides.  | 
| Catalytic activity CATALYTIC ACTIVITY: Reaction=a 2'-deoxyribonucleoside 5'-diphosphate + [thioredoxin]-disulfide + H2O = a ribonucleoside 5'-diphosphate + [thioredoxin]-dithiol; Xref=Rhea:RHEA:23252, Rhea:RHEA-COMP:10698, Rhea:RHEA-COMP:10700, ChEBI:CHEBI:15377, ChEBI:CHEBI:29950, ChEBI:CHEBI:50058, ChEBI:CHEBI:57930, ChEBI:CHEBI:73316; EC=1.17.4.1; Evidence={ECO:0000269|PubMed:16376858};  | 
| Subellular location SUBCELLULAR LOCATION: Cytoplasm.  | 
| Structure SUBUNIT: Heterodimer of a large and a small subunit. Heterodimer with small subunit RRM2 or RRM2B. The heterodimer with RRM2 has higher catalytic activity than the heterodimer with RRM2B. Interacts with AHCYL1 which inhibits its activity. {ECO:0000269|PubMed:16376858, ECO:0000269|PubMed:21336276, ECO:0000269|PubMed:25237103}.  | 
| Involvement in disease DISEASE: Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 6 (PEOB6) [MIM:620647]: A form of progressive external ophthalmoplegia, a mitochondrial myopathy characterized by progressive paralysis of the levator palpebrae, orbicularis oculi, and extraocular muscles. Ragged red fibers are seen on muscle biopsy. {ECO:0000269|PubMed:35617047}. Note=The disease may be caused by variants affecting the gene represented in this entry.  | 
| Target Relevance information above includes information from UniProt accession: P23921 | 
| The UniProt Consortium | 
Data
Publications
| pmid | title | authors | citation | 
|---|---|---|---|
| We haven't added any publications to our database yet. | |||
Protocols
| relevant to this product | 
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| IHC | 
Documents
| # | SDS | Certificate | |
|---|---|---|---|
| Please enter your product and batch number here to retrieve product datasheet, SDS, and QC information. | |||
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