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LC3A/B Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年11月24日
  • W, IF-IC, F
  • Rabbit
  • H,M,R,Mk,C,X,Z,Dg
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    • 详细信息
    • 询价记录
    • 文献和实验
    • 技术资料
    • 抗体英文名

      LC3A/B Antibody

    • 抗原

      synthetic peptide corresponding to residues surrounding Gly40 of LC3B

    • 应用范围

      W, IF-IC, F

    • 宿主

      Rabbit

    • 保质期

      详见说明书

    • 供应商

      CST

    • 适应物种

      H,M,R,Mk,C,X,Z,Dg

    • 库存

      大量

    • 级别

      详见MSDS文件

    • 是否单克隆

      2

    • 保存条件

      -20°c

    • 规格

      100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:carrier free & custom formulation / quantity产品价格:¥请询价

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting  IF-IC=Immunofluorescence (Immunocytochemistry)  F=Flow Cytometry
    Reactivity Key:  H=Human  M=Mouse  R=Rat  Mk=Monkey  C=Chicken  X=Xenopus  Z=Zebrafish  Dg=Dog
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Applications Reactivity Sensitivity MW (kDa) Source
    W IF-IC F H M R (Mk) (C) (X) (Z) (Dg) Endogenous 14, 16 Rabbit
    Protocols

    * Product-specific protocol.

    Specificity / Sensitivity

    LC3A/B Antibody detects endogenous levels of total LC3A and LC3B proteins. Cross-reactivity may exist with LC3C. Stronger reactivity is observed with the type II form of LC3A/B.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Gly40 of LC3B. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from various cell lines, untreated or treated with chloroquine (50 μM, overnight) using LC3A/B Antibody.

    Flow Cytometry

    Flow Cytometry

    Flow cytometric analysis of Hela cells using LC3A/B Antibody (blue) compared to a nonspecific negative control antibody (red).

    IF-IC

    IF-IC

    Confocal immunofluorescent analysis of HeLa cells, untreated (left) or chloroquine-treated (right), using LC3A/B Antibody (green). Actin filaments were labeled using DY-554 phalloidin (red). Blue pseudocolor = DRAQ5® #4084 (fluorescent DNA dye).


    Background

    Autophagy is a catabolic process for the autophagosomic-lysosomal degradation of bulk cytoplasmic contents (1,2). Autophagy is generally activated by conditions of nutrient deprivation but has also been associated with a number of physiological processes including development, differentiation, neurodegenerative diseases, infection and cancer (3). Autophagy marker Light Chain 3 (LC3) was originally identified as a subunit of microtubule-associated proteins 1A and 1B (termed MAP1LC3) (4), and subsequently found to contain similarity to the yeast protein Apg8/Aut7/Cvt5 critical for autophagy (5). Three human LC3 isoforms (LC3A, LC3B, and LC3C) undergo post-translational modifications during autophagy (6-9). Cleavage of LC3 at the carboxy terminus immediately following synthesis yields the cytosolic LC3-I form. During autophagy, LC3-I is converted to LC3-II through lipidation by a ubiquitin-like system involving Atg7 and Atg3 that allows for LC3 to become associated with autophagic vesicles (6-10). The presence of LC3 in autophagosomes and the conversion of LC3 to the lower migrating form LC3-II have been used as indicators of autophagy (11).

    1. Reggiori, F. and Klionsky, D.J. (2002) Eukaryot. Cell 1, 11-21.
    2. Codogno, P. and Meijer, A.J. (2005) Cell Death Differ. 12 Suppl 2, 1509-1518.
    3. Levine, B. and Yuan, J. (2005) J. Clin. Invest. 115, 2679-2688.
    4. Mann, S.S. and Hammarback, J.A. (1994) J. Biol. Chem. 269, 11492-11497.
    5. Lang, T. et al. (1998) EMBO J. 17, 3597-3607.
    6. Kabeya, Y. et al. (2000) EMBO J. 19, 5720-5728.
    7. He, H. et al. (2003) J. Biol. Chem. 278, 29278-29287.
    8. Tanida, I. et al. (2004) J. Biol. Chem. 279, 47704-47710.
    9. Wu, J. et al. (2006) Biochem. Biophys. Res. Commun. 339, 437-442.
    10. Ichimura, Y. et al. (2000) Nature 408, 488-492.
    11. Kabeya, Y. et al. (2004) J. Cell Sci. 117, 2805-2812.
    Application References

    Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know !

    Companion Products

    For Research Use Only. Not For Use In Diagnostic Procedures.

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    图标文献和实验
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    • Detection of Hepatitis B Virus X Antigen by Immunohistochemistry and Western Blotting

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    • Abrogation of p53-Induced Apoptosis by the Hepatitis B Virus X Gene

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    • Antibody Conjugation

      8.0) in clean 16x125mm polypropylene test tube. If needed, adjust pH to 8.0 using 0.5M carbonate buffer. 2. Prepare fresh, 1mg/mL of either NHS-FITC in DMSO or 1mg/mL NHS-LC-Biotin in DH2O. If FITC coupling, add 75uL of FITC/DMSO solution to Antibody

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