LC3B-Specific Polyclonal antibody, PBS Only

LC3B-Specific Polyclonal Antibody for WB, IHC, IF/ICC, FC (Intra), Indirect ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, IHC, IF/ICC, FC (Intra), Indirect ELISA

Conjugate

Unconjugated

Cat no : 18725-1-PBS

Synonyms

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Validation Data Gallery

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  WB analysis of human brain using 18725-1-AP (same clone as 18725-1-PBS)

  human brain tissue were subjected to SDS PAGE followed by western blot with 18725-1-AP (LC3B-Specific antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

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  WB analysis of TN treated Hela using 18725-1-AP (same clone as 18725-1-PBS)

  TN treated Hela cells were subjected to SDS PAGE followed by western blot with 18725-1-AP (LC3B-Specific antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

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  WB analysis of A549 using 18725-1-AP (same clone as 18725-1-PBS)

  A549 cells were subjected to SDS PAGE followed by western blot with 18725-1-AP (LC3B-Specific antibody) at dilution of 1:500 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

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  WB analysis using 18725-1-AP (same clone as 18725-1-PBS)

  HepG2 cells were subjected to SDS PAGE followed by western blot with 18725-1-AP (LC3B-Specific antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

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  WB analysis of mouse brain using 18725-1-AP (same clone as 18725-1-PBS)

  mouse brain tissue were subjected to SDS PAGE followed by western blot with 18725-1-AP (LC3B-Specific antibody) at dilution of 1:300 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

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  WB analysis of MCF-7 using 18725-1-AP (same clone as 18725-1-PBS)

  MCF7 cells were subjected to SDS PAGE followed by western blot with 18725-1-AP (LC3B-Specific antibody) at dilution of 1:500 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

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  WB analysis of UV treated HEK-293 using 18725-1-AP (same clone as 18725-1-PBS)

  UV treated HEK-293 cells were subjected to SDS PAGE followed by western blot with 18725-1-AP (LC3B-Specific antibody) at dilution of 1:300 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

• 

  IHC staining of mouse brain using 18725-1-AP (same clone as 18725-1-PBS)

  Immunohistochemical analysis of paraffin-embedded mouse brain tissue slide using 18725-1-AP (LC3B-Specific antibody) at dilution of 1:200 (under 40x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

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  IHC staining of mouse brain using 18725-1-AP (same clone as 18725-1-PBS)

  Immunohistochemical analysis of paraffin-embedded mouse brain tissue slide using 18725-1-AP (LC3B-Specific antibody) at dilution of 1:200 (under 10x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

• 

  IHC staining of mouse brain using 18725-1-AP (same clone as 18725-1-PBS)

  Immunohistochemical analysis of paraffin-embedded mouse brain tissue slide using 18725-1-AP (LC3B-Specific antibody) at dilution of 1:200 (under 40x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

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  IHC staining of rat brain using 18725-1-AP (same clone as 18725-1-PBS)

  Immunohistochemical analysis of paraffin-embedded rat brain tissue slide using 18725-1-AP (LC3B-Specific antibody) at dilution of 1:200 (under 10x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

• 

  IHC staining of rat brain using 18725-1-AP (same clone as 18725-1-PBS)

  Immunohistochemical analysis of paraffin-embedded rat brain tissue slide using 18725-1-AP (LC3B-Specific antibody) at dilution of 1:200 (under 40x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

• 

  IHC staining of rat brain using 18725-1-AP (same clone as 18725-1-PBS)

  Immunohistochemical analysis of paraffin-embedded rat brain tissue slide using 18725-1-AP (LC3B-Specific antibody) at dilution of 1:200 (under 10x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

• 

  IHC staining of mouse brain using 18725-1-AP (same clone as 18725-1-PBS)

  Immunohistochemical analysis of paraffin-embedded mouse brain tissue slide using 18725-1-AP (LC3B-Specific antibody) at dilution of 1:200 (under 10x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

• 

  IHC staining of rat brain using 18725-1-AP (same clone as 18725-1-PBS)

  Immunohistochemical analysis of paraffin-embedded rat brain tissue slide using 18725-1-AP (LC3B-Specific antibody) at dilution of 1:200 (under 40x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

• 

  IF Staining of HepG2 using 18725-1-AP (same clone as 18725-1-PBS)

  Immunofluorescent analysis of -20℃ Ethanol fixed CQ treated HepG2 cells (left) and untreated HepG2 cells (right) using 18725-1-AP (LC3B-Specific antibody) at dilution of 1:50 and Alexa Fluor 488-conjugated AffiniPure Goat Anti-Rabbit IgG(H+L). The cytoskeleton was labelled in red with 66031-1-Ig (alpha tubulin). This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

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  IF Staining of HeLa using 18725-1-AP (same clone as 18725-1-PBS)

  Immunofluorescent analysis of (-20°C Ethanol) fixed Chloroquine treated HeLa cells using LC3B-Specific antibody (18725-1-AP) at dilution of 1:200 and CoraLite®488-Conjugated AffiniPure Goat Anti-Rabbit IgG(H+L), CL594-Phalloidin (red). This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

• 

  IF Staining of HepG2 using 18725-1-AP (same clone as 18725-1-PBS)

  Immunofluorescent analysis of (-20°C Ethanol) fixed CQ treated HepG2 cells using 18725-1-AP (LC3B-Specific antibody) at dilution of 1:200 and CoraLite488-Conjugated AffiniPure Goat Anti-Rabbit IgG(H+L). This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

• 

  IF Staining of HepG2 using 18725-1-AP (same clone as 18725-1-PBS)

  Immunofluorescent analysis of (-20°C Ethanol) fixed HepG2 cells using 18725-1-AP (LC3B-Specific antibody) at dilution of 1:200 and CoraLite488-Conjugated AffiniPure Goat Anti-Rabbit IgG(H+L). This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

• 

  FC experiment of HeLa using 18725-1-AP (same clone as 18725-1-PBS)

  1X10^6 HeLa cells were intracellularly stained with 0.4 ug Anti-Human LC3B-Specific (18725-1-AP) and CoraLite®488-Conjugated AffiniPure Goat Anti-Rabbit IgG(H+L) at dilution 1:1000 (red), or 0.4 ug Control Antibody. Cells were fixed with 4% PFA and permeabilized with Flow Cytometry Perm Buffer (PF00011-C). This data was developed using the same antibody clone with 18725-1-PBS in a different storage buffer formulation.

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Product Information

18725-1-PBS targets LC3B-Specific in WB, IHC, IF/ICC, FC (Intra), Indirect ELISA applications and shows reactivity with human, mouse, rat samples.

• Tested Reactivity: human, mouse, rat
• Host / Isotype: Rabbit / IgG
• Class: Polyclonal
• Type: Antibody
• Immunogen: Peptide
• Full Name: microtubule-associated protein 1 light chain 3 beta
• Calculated Molecular Weight: 15 kDa
• Observed Molecular Weight: 15 kDa, 18 kDa
• GenBank Accession Number: NM_022818
• Gene Symbol: LC3B
• Gene ID (NCBI): 81631
• Conjugate: Unconjugated
• Form: Liquid
• Purification Method: Antigen affinity purification
• Storage Buffer: PBS Only
• Storage Conditions: Store at -80°C.

Background Information

LC3B, also named as MAP1LC3B, MAP1A/1BLC3, belongs to the MAP1 LC3 family. It is a subunit of neuronal microtubule-associated MAP1A and MAP1B proteins, which are involved in microtubule assembly and important for neurogenesis. In cell biology, autophagy, or autophagocytosis, is a catabolic process involving the degradation of a cell's own components through the lysosomalmachinery. It is a major mechanism by which a starving cell reallocates nutrients from unnecessary processes to more-essential processes. Two forms of LC3, called LC3-I (17-19kd) and -II(14-16kd), were produced post-translationally in various cells. LC3-I is cytosolic, whereas LC3-II is membrane bound. The precursor molecule is cleaved by APG4B/ATG4B to form the cytosolic form, LC3-I. This is activated by APG7L/ATG7, transferred to ATG3 and conjugated to phospholipid to form the membrane-bound form, LC3-II. The amount of LC3-II is correlated with the extent of autophagosome formation. LC3-II is the first mammalian protein identified that specifically associates with autophagosome membranes. MAP1LC3 has 3 isoforms MAP1LC3A, MAP1LC3B and MAP1LC3C. MAP1LC3A and MAP1LC3C are produced by the proteolytic cleavage after the conserved C-terminal Gly residue, like their rat counterpart, MAP1LC3B does not undergo C-terminal cleavage and exists in a single modified form. This antibody is specific to LC3B.