Anti-L-Lactyl-Histone H3 (Lys27) Rabbit pAb
PTM-1428
ApplicationsWestern Blot, ChIP Chromatin ImmunoPrecipitation
Product group Antibodies
ReactivityHuman, Mouse
Overview
- SupplierPTM BIO
- Product NameAnti-L-Lactyl-Histone H3 (Lys27) Rabbit pAb
- Delivery Days Customer5
- Antibody SpecificityAnti-L-Lactyl-Histone H3 (Lys27) Rabbit pAb detects histone H3 only when it is L-lactylated at Lys27.
- ApplicationsWestern Blot, ChIP Chromatin ImmunoPrecipitation
- Applications SupplierWB, ChIP
- Category SupplierAntibody
- CertificationResearch Use Only
- ClonalityPolyclonal
- Clone IDW1664-FT3
- ConjugateUnconjugated
- HostRabbit
- IsotypeIgG
- Protein IDP68431
- Protein NameHistone H3.1
- Scientific DescriptionHistones, fundamental proteins involved in chromatin structure and gene regulation, are subject to a wide array of enzyme-catalyzed modifications, including acetylation, methylation, Phosphorylatedrylation, ubiquitination, and numerous others. Histone L-lactylation, a recently discovered post-translational modification induced by lactate has emerged as a significant addition to this repertoire. The extent and dynamics of this modification are highly reliant on lactate levels within the cellular microenvironment and can be modulated through the introduction of extracellular lactate in cultured cells or the stimulation of intracellular glycolysis. The introduction of lysine L-lactylation is mediated by the acetyltransferase p300, while the removal of lactylation marks from histones has been attributed to Class I histone deacetylases (HDAC 1-3). Histone lactylation has been implicated in various biological processes, including inflammation, fibrosis, differentiation, and cancer progression.
- Shelf life instructionStable for 12 months from date of receipt/reconstitution.
- ReactivityHuman, Mouse
- Reactivity SupplierHuman, Mouse
- Reactivity Supplier NoteProtein A and immunogen affinity purified
- Storage InstructionStore at -20°C. Avoid freeze/thaw cycles.
- UNSPSC12352203
References
- Xuanxuan Zhang, et al. 'Lactate drives epithelial-mesenchymal transition in diabetic kidney disease via the H3K14la/KLF5 pathway' Redox Biology (2024)Read more