Product Name
SIRT5 Recombinant Rabbit Monoclonal Antibody [PSH15-71] - BSA and Azide free
Antibody Type
Recombinant Rabbit monoclonal Antibody
Target Molecular Weight
Predicted band size: 34 kDa
Positive Control
293T cell lysate, Hepa-1-6 cell lysate, RAW264.7 cell lysate, C6 cell lysate, Rat liver tissue lysate, human liver tissue.
Storage Instructions
Store at 2-8℃. Avoid freeze.
Purification Method
Protein A affinity purified.
Function
SIRT5 is a human member of a family of proteins called Sirtuins (Sir2-like proteins) and are present in prokaryotes and eukaryotes. All Sir2-like proteins have a sirtuin core domain, which contains a series of sequence motifs conserved in organisms ranging from bacteria to humans. Bacterial, yeast and mammalian sirtuins are able to metabolize NAD and possibly at as mono-ADP-ribosyltransferases. The enzymatic function of sirtuins is not yet completely understood but recent reports of histone-activated Sir2-mediated NAD metabolism and NAD-activated Sir2-mediated histone deacetylation suggest a possible coupled reciprocal activation mechanism involving interactions of Sir2 with NAD and the N epsilon-acetyl-lysine groups of acetylated histones.
Background References
1. Teng P et al. SIRT5-mediated ME2 desuccinylation promotes cancer growth by enhancing mitochondrial respiration. Cell Death Differ. 2024 Jan
2. Wu M et al. Sirt5 improves cardiomyocytes fatty acid metabolism and ameliorates cardiac lipotoxicity in diabetic cardiomyopathy via CPT2 de-succinylation. Redox Biol. 2024 Jul
Subcellular Location
Mitochondrion matrix, Mitochondrion intermembrane space, Cytoplasm, cytosol, Nucleus.
Synonyms
NAD dependent deacetylase sirtuin 5 antibody
NAD dependent lysine demalonylase and desuccinylase sirtuin 5 mitochondrial antibody
NAD dependent protein deacylase sirtuin 5 mitochondrial antibody
NAD-dependent protein deacylase sirtuin-5, mitochondrial antibody
Regulatory protein SIR2 homolog 5 antibody
Silent mating type information regulation 2 S.cerevisiae homolog 5 antibody
Sir2 like 5 antibody
SIR2-like protein 5 antibody
SIR2L5 antibody
SIR5_HUMAN antibody
Expand
NAD dependent deacetylase sirtuin 5 antibody
NAD dependent lysine demalonylase and desuccinylase sirtuin 5 mitochondrial antibody
NAD dependent protein deacylase sirtuin 5 mitochondrial antibody
NAD-dependent protein deacylase sirtuin-5, mitochondrial antibody
Regulatory protein SIR2 homolog 5 antibody
Silent mating type information regulation 2 S.cerevisiae homolog 5 antibody
Sir2 like 5 antibody
SIR2-like protein 5 antibody
SIR2L5 antibody
SIR5_HUMAN antibody
Sirt5 antibody
Sirtuin 5 antibody
Sirtuin type 5 antibody
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This data was developed using HA723774, the same antibody clone in a different buffer formulation.
Western blot analysis of SIRT5 on different lysates with Rabbit anti-SIRT5 antibody (HA723774) at 1/2,000 dilution.
Lane 1: 293T cell lysate (20 µg/Lane)
Lane 2: Hepa-1-6 cell lysate (20 µg/Lane)
Lane 3: RAW264.7 cell lysate (20 µg/Lane)
Lane 4: C6 cell lysate (20 µg/Lane)
Lane 5: Rat liver tissue lysate (20 µg/Lane)
Predicted band size: 34 kDa
Observed band size: 34 kDa
Exposure time: 1 minute 50 seconds; ECL: K1801;
4-20% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA723774) at 1/2,000 dilution was used in primary antibody dilution (K1803) at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
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This data was developed using HA723774, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human liver tissue with Rabbit anti-SIRT5 antibody (HA723774) at 1/1,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA723774) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"