membrane protein 2 lamp2 Search Results


rat monoclonal anti lamp 2  (StressMarq)
92
StressMarq rat monoclonal anti lamp 2
Rat Monoclonal Anti Lamp 2, supplied by StressMarq, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/membrane+protein+2+lamp2/Anti-LAMP2+Antibody/pmc11289521-262-49-54
Average 92 stars, based on 1 article reviews
rat monoclonal anti lamp 2 - by Bioz Stars, 2026-10
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lamp2a  (MedChemExpress)
93
MedChemExpress lamp2a
Lamp2a, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/membrane+protein+2+lamp2/LAMP2+Antibody/pm41407230-147-79-82
Average 93 stars, based on 1 article reviews
lamp2a - by Bioz Stars, 2026-10
93/100 stars
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lamp2  (Boster Bio)
94
Boster Bio lamp2
Lamp2, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/membrane+protein+2+lamp2/Anti-LAMP2a+Rabbit+Monoclonal+Antibody/pmc12907057-303-47-48
Average 94 stars, based on 1 article reviews
lamp2 - by Bioz Stars, 2026-10
94/100 stars
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lamp2  (ProSci Incorporated)
90
ProSci Incorporated lamp2
RACK1 depletion-induced autophagy is non-canonical. ( a ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 48 h, followed by immunoblot analysis using the indicated antibodies (left panel). Intensities of Atg5/12 and Beclin1 proteins were normalized against that of tubulin proteins, and the relative expressions in RACK1 siRNA-treated cells compared with that in control cells were plotted (right panel). ( b ) HT1080 cells were transfected with siRNAs against control or RACK1 in combination with or without Beclin1 siRNA (100 pmol). After 48 h, these cells were analyzed by immunoblotting using the indicated antibodies. ( c ) HT1080 cells were transfected with control or Atg5 siRNA (100 pmol). After 24 h, the cells were re-transfected with control or RACK1 siRNA. After a further 48 h incubation, the cell extracts were subjected to immunoblot analysis using the indicated antibodies. ( d ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 48 h, followed by immunoblot analysis using the indicated antibodies. ( e ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 24 h. Extracts of siRNA-transfected cells were pretreated with rapamycin 1 μM for 24 h, followed by immunoblot analysis using the indicated antibodies. Intensities of LAMP1 and <t>LAMP2</t> proteins were normalized against that of tubulin proteins, and the relative expressions in RACK1 siRNA-treated cells compared with that in control cells were plotted. * P <0.05, ** P <0.01 (Student’s t -test)
Lamp2, supplied by ProSci Incorporated, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/membrane+protein+2+lamp2/LAMP2+Antibody/pmc05520723-138-8-12
Average 90 stars, based on 1 article reviews
lamp2 - by Bioz Stars, 2026-10
90/100 stars
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antibody specific to human lamp1  (Johns Hopkins HealthCare)
90
Johns Hopkins HealthCare antibody specific to human lamp1
RACK1 depletion-induced autophagy is non-canonical. ( a ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 48 h, followed by immunoblot analysis using the indicated antibodies (left panel). Intensities of Atg5/12 and Beclin1 proteins were normalized against that of tubulin proteins, and the relative expressions in RACK1 siRNA-treated cells compared with that in control cells were plotted (right panel). ( b ) HT1080 cells were transfected with siRNAs against control or RACK1 in combination with or without Beclin1 siRNA (100 pmol). After 48 h, these cells were analyzed by immunoblotting using the indicated antibodies. ( c ) HT1080 cells were transfected with control or Atg5 siRNA (100 pmol). After 24 h, the cells were re-transfected with control or RACK1 siRNA. After a further 48 h incubation, the cell extracts were subjected to immunoblot analysis using the indicated antibodies. ( d ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 48 h, followed by immunoblot analysis using the indicated antibodies. ( e ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 24 h. Extracts of siRNA-transfected cells were pretreated with rapamycin 1 μM for 24 h, followed by immunoblot analysis using the indicated antibodies. Intensities of LAMP1 and <t>LAMP2</t> proteins were normalized against that of tubulin proteins, and the relative expressions in RACK1 siRNA-treated cells compared with that in control cells were plotted. * P <0.05, ** P <0.01 (Student’s t -test)
Antibody Specific To Human Lamp1, supplied by Johns Hopkins HealthCare, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/membrane+protein+2+lamp2/lysosome+associated+membrane+protein+2++lamp2+++abl+93++antibody/pm20522958-193-24-7
Average 90 stars, based on 1 article reviews
antibody specific to human lamp1 - by Bioz Stars, 2026-10
90/100 stars
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anti-lamp2 rabbit polyclonal antibody  (Bioworld Antibodies)
90
Bioworld Antibodies anti-lamp2 rabbit polyclonal antibody
RACK1 depletion-induced autophagy is non-canonical. ( a ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 48 h, followed by immunoblot analysis using the indicated antibodies (left panel). Intensities of Atg5/12 and Beclin1 proteins were normalized against that of tubulin proteins, and the relative expressions in RACK1 siRNA-treated cells compared with that in control cells were plotted (right panel). ( b ) HT1080 cells were transfected with siRNAs against control or RACK1 in combination with or without Beclin1 siRNA (100 pmol). After 48 h, these cells were analyzed by immunoblotting using the indicated antibodies. ( c ) HT1080 cells were transfected with control or Atg5 siRNA (100 pmol). After 24 h, the cells were re-transfected with control or RACK1 siRNA. After a further 48 h incubation, the cell extracts were subjected to immunoblot analysis using the indicated antibodies. ( d ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 48 h, followed by immunoblot analysis using the indicated antibodies. ( e ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 24 h. Extracts of siRNA-transfected cells were pretreated with rapamycin 1 μM for 24 h, followed by immunoblot analysis using the indicated antibodies. Intensities of LAMP1 and <t>LAMP2</t> proteins were normalized against that of tubulin proteins, and the relative expressions in RACK1 siRNA-treated cells compared with that in control cells were plotted. * P <0.05, ** P <0.01 (Student’s t -test)
Anti Lamp2 Rabbit Polyclonal Antibody, supplied by Bioworld Antibodies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/membrane+protein+2+lamp2/lysosomal+associated+membrane+protein+2++lamp+2/ppr0282580-59-12-18
Average 90 stars, based on 1 article reviews
anti-lamp2 rabbit polyclonal antibody - by Bioz Stars, 2026-10
90/100 stars
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primary antibodies against human cd107b (lysosome-associated membrane protein-2, lamp-2) #10-672-c100  (HiSS Diagnostics)
90
HiSS Diagnostics primary antibodies against human cd107b (lysosome-associated membrane protein-2, lamp-2) #10-672-c100
RACK1 depletion-induced autophagy is non-canonical. ( a ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 48 h, followed by immunoblot analysis using the indicated antibodies (left panel). Intensities of Atg5/12 and Beclin1 proteins were normalized against that of tubulin proteins, and the relative expressions in RACK1 siRNA-treated cells compared with that in control cells were plotted (right panel). ( b ) HT1080 cells were transfected with siRNAs against control or RACK1 in combination with or without Beclin1 siRNA (100 pmol). After 48 h, these cells were analyzed by immunoblotting using the indicated antibodies. ( c ) HT1080 cells were transfected with control or Atg5 siRNA (100 pmol). After 24 h, the cells were re-transfected with control or RACK1 siRNA. After a further 48 h incubation, the cell extracts were subjected to immunoblot analysis using the indicated antibodies. ( d ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 48 h, followed by immunoblot analysis using the indicated antibodies. ( e ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 24 h. Extracts of siRNA-transfected cells were pretreated with rapamycin 1 μM for 24 h, followed by immunoblot analysis using the indicated antibodies. Intensities of LAMP1 and <t>LAMP2</t> proteins were normalized against that of tubulin proteins, and the relative expressions in RACK1 siRNA-treated cells compared with that in control cells were plotted. * P <0.05, ** P <0.01 (Student’s t -test)
Primary Antibodies Against Human Cd107b (Lysosome Associated Membrane Protein 2, Lamp 2) #10 672 C100, supplied by HiSS Diagnostics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/membrane+protein+2+lamp2/primary+antibodies+against+human+cd107b++lysosome+associated+membrane+protein+2++lamp+2+++10+672+c100/pmc04869830-182-13-20
Average 90 stars, based on 1 article reviews
primary antibodies against human cd107b (lysosome-associated membrane protein-2, lamp-2) #10-672-c100 - by Bioz Stars, 2026-10
90/100 stars
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elisa kit for lysosomal associated membrane protein 2 (lamp2; cat. # seb464hu)  (Cloud-Clone corp)
90
Cloud-Clone corp elisa kit for lysosomal associated membrane protein 2 (lamp2; cat. # seb464hu)
RACK1 depletion-induced autophagy is non-canonical. ( a ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 48 h, followed by immunoblot analysis using the indicated antibodies (left panel). Intensities of Atg5/12 and Beclin1 proteins were normalized against that of tubulin proteins, and the relative expressions in RACK1 siRNA-treated cells compared with that in control cells were plotted (right panel). ( b ) HT1080 cells were transfected with siRNAs against control or RACK1 in combination with or without Beclin1 siRNA (100 pmol). After 48 h, these cells were analyzed by immunoblotting using the indicated antibodies. ( c ) HT1080 cells were transfected with control or Atg5 siRNA (100 pmol). After 24 h, the cells were re-transfected with control or RACK1 siRNA. After a further 48 h incubation, the cell extracts were subjected to immunoblot analysis using the indicated antibodies. ( d ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 48 h, followed by immunoblot analysis using the indicated antibodies. ( e ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 24 h. Extracts of siRNA-transfected cells were pretreated with rapamycin 1 μM for 24 h, followed by immunoblot analysis using the indicated antibodies. Intensities of LAMP1 and <t>LAMP2</t> proteins were normalized against that of tubulin proteins, and the relative expressions in RACK1 siRNA-treated cells compared with that in control cells were plotted. * P <0.05, ** P <0.01 (Student’s t -test)
Elisa Kit For Lysosomal Associated Membrane Protein 2 (Lamp2; Cat. # Seb464hu), supplied by Cloud-Clone corp, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/membrane+protein+2+lamp2/ELISA+Kit+for+Lysosomal+Associated+Membrane+Protein+2++LAMP2++cat++++SEB464Hu/pmc05952035-51-5-18
Average 90 stars, based on 1 article reviews
elisa kit for lysosomal associated membrane protein 2 (lamp2; cat. # seb464hu) - by Bioz Stars, 2026-10
90/100 stars
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anti-lamp-2(lysosomal-associated membrane protein 2) pe  (Bioquote Inc)
90
Bioquote Inc anti-lamp-2(lysosomal-associated membrane protein 2) pe
RACK1 depletion-induced autophagy is non-canonical. ( a ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 48 h, followed by immunoblot analysis using the indicated antibodies (left panel). Intensities of Atg5/12 and Beclin1 proteins were normalized against that of tubulin proteins, and the relative expressions in RACK1 siRNA-treated cells compared with that in control cells were plotted (right panel). ( b ) HT1080 cells were transfected with siRNAs against control or RACK1 in combination with or without Beclin1 siRNA (100 pmol). After 48 h, these cells were analyzed by immunoblotting using the indicated antibodies. ( c ) HT1080 cells were transfected with control or Atg5 siRNA (100 pmol). After 24 h, the cells were re-transfected with control or RACK1 siRNA. After a further 48 h incubation, the cell extracts were subjected to immunoblot analysis using the indicated antibodies. ( d ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 48 h, followed by immunoblot analysis using the indicated antibodies. ( e ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 24 h. Extracts of siRNA-transfected cells were pretreated with rapamycin 1 μM for 24 h, followed by immunoblot analysis using the indicated antibodies. Intensities of LAMP1 and <t>LAMP2</t> proteins were normalized against that of tubulin proteins, and the relative expressions in RACK1 siRNA-treated cells compared with that in control cells were plotted. * P <0.05, ** P <0.01 (Student’s t -test)
Anti Lamp 2(lysosomal Associated Membrane Protein 2) Pe, supplied by Bioquote Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/membrane+protein+2+lamp2/anti+lamp+2+lysosomal+associated+membrane+protein+2++pe/pmc03316510-78-18-25
Average 90 stars, based on 1 article reviews
anti-lamp-2(lysosomal-associated membrane protein 2) pe - by Bioz Stars, 2026-10
90/100 stars
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human lysosomal associated membrane protein 2 (lamp2) elisa kit  (Bioss)
N/A
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lysosomal associated membrane protein 2 lamp2 antibody biotin  (Abbexa)
N/A
Lysosomal Associated Membrane Protein 2 LAMP2 Antibody Biotin is an antibody conjugated to Biotin against Lysosomal Associated Membrane Protein 2 LAMP2
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lamp2 human - recombinant human lysosomal-associated membrane protein 2  (Aviva Systems)
N/A
Product Introduction: The protein encoded by LAMP2 belongs to a family of membrane glycoproteins. This glycoprotein provides selectins with carbohydrate ligands LAMP2 takes part in tumor cell metastasis and in addition has a role in
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Image Search Results


RACK1 depletion-induced autophagy is non-canonical. ( a ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 48 h, followed by immunoblot analysis using the indicated antibodies (left panel). Intensities of Atg5/12 and Beclin1 proteins were normalized against that of tubulin proteins, and the relative expressions in RACK1 siRNA-treated cells compared with that in control cells were plotted (right panel). ( b ) HT1080 cells were transfected with siRNAs against control or RACK1 in combination with or without Beclin1 siRNA (100 pmol). After 48 h, these cells were analyzed by immunoblotting using the indicated antibodies. ( c ) HT1080 cells were transfected with control or Atg5 siRNA (100 pmol). After 24 h, the cells were re-transfected with control or RACK1 siRNA. After a further 48 h incubation, the cell extracts were subjected to immunoblot analysis using the indicated antibodies. ( d ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 48 h, followed by immunoblot analysis using the indicated antibodies. ( e ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 24 h. Extracts of siRNA-transfected cells were pretreated with rapamycin 1 μM for 24 h, followed by immunoblot analysis using the indicated antibodies. Intensities of LAMP1 and LAMP2 proteins were normalized against that of tubulin proteins, and the relative expressions in RACK1 siRNA-treated cells compared with that in control cells were plotted. * P <0.05, ** P <0.01 (Student’s t -test)

Journal: Cell Death & Disease

Article Title: RACK1 depletion in the ribosome induces selective translation for non-canonical autophagy

doi: 10.1038/cddis.2017.204

Figure Lengend Snippet: RACK1 depletion-induced autophagy is non-canonical. ( a ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 48 h, followed by immunoblot analysis using the indicated antibodies (left panel). Intensities of Atg5/12 and Beclin1 proteins were normalized against that of tubulin proteins, and the relative expressions in RACK1 siRNA-treated cells compared with that in control cells were plotted (right panel). ( b ) HT1080 cells were transfected with siRNAs against control or RACK1 in combination with or without Beclin1 siRNA (100 pmol). After 48 h, these cells were analyzed by immunoblotting using the indicated antibodies. ( c ) HT1080 cells were transfected with control or Atg5 siRNA (100 pmol). After 24 h, the cells were re-transfected with control or RACK1 siRNA. After a further 48 h incubation, the cell extracts were subjected to immunoblot analysis using the indicated antibodies. ( d ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 48 h, followed by immunoblot analysis using the indicated antibodies. ( e ) HT1080 cells transfected with control or RACK1 siRNAs (50 pmol) were incubated for 24 h. Extracts of siRNA-transfected cells were pretreated with rapamycin 1 μM for 24 h, followed by immunoblot analysis using the indicated antibodies. Intensities of LAMP1 and LAMP2 proteins were normalized against that of tubulin proteins, and the relative expressions in RACK1 siRNA-treated cells compared with that in control cells were plotted. * P <0.05, ** P <0.01 (Student’s t -test)

Article Snippet: Antibodies against Atg5, Atg9A, Atg4B, Atg16, LAMP1 and LAMP2 were obtained from ProSci (Poway, CA, USA), and the anti-rpS3 antibody was from HAEL (Seoul, Korea).

Techniques: Transfection, Control, Incubation, Western Blot