• Jia, Wei‐Qiang, et al. "Verbascoside inhibits progression of glioblastoma cells by promoting Let‐7g‐5p and down‐regulating HMGA2 via Wnt/beta‐catenin signalling blockade. " Journal of cellular and molecular medicine 24. 5 (2020) : 2901-2916.
  • Immunofluorescence analysis of Hela cell. 1, Cleaved-PARP-1 (D214) Polyclonal Antibody (red) was diluted at 1:200 (4°C overnight). LC3B Polyclonal Antibody (green) was diluted at 1:200 (4°C overnight). 2, Goat Anti Rabbit Alexa Fluor 594 Catalog:STJS000476 was diluted at 1:1000 (room temperature, 50min). Goat Anti mouse Alexa Fluor 488 Catalog:STJS000301 was diluted at 1:1000 (room temperature, 50min).
  • Western blot analysis of lysates from 1) Hela, 2) 3T3, 3) Rat Brain Tissue cells, (Green) primary antibody was diluted at 1:1000, 4°C over night, secondary antibody (STJS000791) was diluted at 1:10000, 37° 1hour. (Red) GAPDH Monoclonal Antibody (2B8) (STJ96931) antibody was diluted at 1:5000 as loading control, 4° over night, secondary antibody (STJS000788) was diluted at 1:10000, 37° 1hour.
  • Immunohistochemical analysis of paraffin-embedded Rat-kidney tissue. 1, LC3B Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.
  • Immunohistochemical analysis of paraffin-embedded mouse-lung tissue. 1, LC3B Polyclonal Antibody was diluted at 1:200 (4°C, overnight). 2, Sodium citrate pH 6.0 was used for antibody retrieval (>98°C, 20min). 3, Secondary antibody was diluted at 1:200 (room tempeRature, 30min). Negative control was used by secondary antibody only.
  • Immunofluorescence analysis of mouse-lung tissue. 1, LC3B Polyclonal Antibody (red) was diluted at 1:200 (4°C, overnight). 2, Cy3 labelled Secondary antibody was diluted at 1:300 (room temperature, 50min). 3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+B
  • Western blot analysis of 1) Hela, 2) 3T3, 3) Rat Brain Tissue using MAP LC3β Polyclonal Antibody. Secondary antibody (STJ99666) was diluted at 1:20000
  • Immunohistochemical analysis of paraffin-embedded Rat BrainTissue using MAP LC3β Polyclonal Antibody.
  • Feng, Qin. "Quantitative proteomic analysis reveals that Arctigenin alleviates concanavalin A-induced hepatitis through suppressing immune system and regulating autophagy. " Frontiers in immunology 9 (2018) : 1881.

Anti-MAP1LC3B antibody (STJ197355)

SKU:
STJ197355

Current Stock:
Host: Rabbit
Applications: WB/IF/IHC
Reactivity: Human/Mouse/Rat
Note: STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.
Short Description: Rabbit polyclonal antibody anti-Microtubule-associated proteins 1A/1B light chain 3B is suitable for use in Western Blot, Immunofluorescence and Immunohistochemistry research applications.
Clonality: Polyclonal
Conjugation: Unconjugated
Isotype: IgG
Formulation: Liquid in PBS pH7.4, 0.5% BSA, 0.02% Sodium Azide and 50% Glycerol.
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Dilution Range: WB 1:1000-2000
IHC 1:200-500
IF 1:200
Storage Instruction: Store at-20°C for up to 1 year from the date of receipt, and avoid repeat freeze-thaw cycles.
Gene Symbol: MAP1LC3B
Gene ID: 81631
Uniprot ID: MLP3B_HUMAN
Specificity: The antibody detects endogenous MAP LC3 Beta protein.
Immunogen: Recombinant Protein of MAP LC3 Beta
Post Translational Modifications The precursor molecule is cleaved by ATG4 (ATG4A, ATG4B, ATG4C or ATG4D) to expose the glycine at the C-terminus and form the cytosolic form, LC3-I. The processed form is then activated by APG7L/ATG7, transferred to ATG3 and conjugated to phosphatidylethanolamine (PE) phospholipid to form the membrane-bound form, LC3-II. During non-canonical autophagy, the processed form is conjugated to phosphatidylserine (PS) phospholipid. ATG4 proteins also mediate the delipidation of PE-conjugated forms. In addition, ATG4B and ATG4D mediate delipidation of ATG8 proteins conjugated to PS during non-canonical autophagy. ATG4B constitutes the major protein for proteolytic activation. ATG4D is the main enzyme for delipidation activity. (Microbial infection) The Legionella effector RavZ is a deconjugating enzyme that hydrolyzes the amide bond between the C-terminal glycine residue and an adjacent aromatic residue in ATG8 proteins conjugated to phosphatidylethanolamine (PE), producing an ATG8 protein that is resistant to reconjugation by the host machinery due to the cleavage of the reactive C-terminal glycine. RavZ is also able to mediate delipidation of ATG8 proteins conjugated to phosphatidylserine (PS). Phosphorylation by PKA inhibits conjugation of phosphatidylethanolamine (PE). Interaction with MAPK15 reduces the inhibitory phosphorylation and increases autophagy activity.
Function Ubiquitin-like modifier involved in formation of autophagosomal vacuoles (autophagosomes). Plays a role in mitophagy which contributes to regulate mitochondrial quantity and quality by eliminating the mitochondria to a basal level to fulfill cellular energy requirements and preventing excess ROS production. In response to cellular stress and upon mitochondria fission, binds C-18 ceramides and anchors autophagolysosomes to outer mitochondrial membranes to eliminate damaged mitochondria. While LC3s are involved in elongation of the phagophore membrane, the GABARAP/GATE-16 subfamily is essential for a later stage in autophagosome maturation. Promotes primary ciliogenesis by removing OFD1 from centriolar satellites via the autophagic pathway. Through its interaction with the reticulophagy receptor TEX264, participates in the remodeling of subdomains of the endoplasmic reticulum into autophagosomes upon nutrient stress, which then fuse with lysosomes for endoplasmic reticulum turnover. Upon nutrient stress, directly recruits cofactor JMY to the phagophore membrane surfaces and promotes JMY's actin nucleation activity and autophagosome biogenesis during autophagy.
Protein Name Microtubule-Associated Proteins 1a/1b Light Chain 3b
Autophagy-Related Protein Lc3 B
Autophagy-Related Ubiquitin-Like Modifier Lc3 B
Map1 Light Chain 3-Like Protein 2
Map1a/Map1b Light Chain 3 B
Map1a/Map1b Lc3 B
Microtubule-Associated Protein 1 Light Chain 3 Beta
Database Links Reactome: R-HSA-1632852
Reactome: R-HSA-5205685
Reactome: R-HSA-8854214
Reactome: R-HSA-8934903
Reactome: R-HSA-9664873
Reactome: R-HSA-9679504
Reactome: R-HSA-9694676
Reactome: R-HSA-9754560
Reactome: R-HSA-9755511
Cellular Localisation Cytoplasmic Vesicle
Autophagosome Membrane
Lipid-Anchor
Endomembrane System
Mitochondrion Membrane
Cytoplasm
Cytoskeleton
Lc3-Ii Binds To The Autophagic Membranes
Lc3-Ii Localizes With The Mitochondrial Inner Membrane During Parkin-Mediated Mitophagy
Localizes Also To Discrete Punctae Along The Ciliary Axoneme
Alternative Antibody Names Anti-Microtubule-Associated Proteins 1a/1b Light Chain 3b antibody
Anti-Autophagy-Related Protein Lc3 B antibody
Anti-Autophagy-Related Ubiquitin-Like Modifier Lc3 B antibody
Anti-Map1 Light Chain 3-Like Protein 2 antibody
Anti-Map1a/Map1b Light Chain 3 B antibody
Anti-Map1a/Map1b Lc3 B antibody
Anti-Microtubule-Associated Protein 1 Light Chain 3 Beta antibody
Anti-MAP1LC3B antibody
Anti-MAP1ALC3 antibody

Information sourced from Uniprot.org

12 months for antibodies. 6 months for ELISA Kits. Please see website T&Cs for further guidance