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ABclonal Biotechnology pum1 primary antibody
a <t>PUM1</t> mRNA expression levels in PAAD tissues (T) and normal tissues (N) analyzed by gene expression profiling interactive analysis (GEPIA). * P < 0.05. b Analysis of the relationship between PUM1 mRNA expression and overall survival of PAAD patients analyzed using The Cancer Genome Atlas (TCGA)
Pum1 Primary Antibody, supplied by ABclonal Biotechnology, 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/result/pum1 primary antibody/product/ABclonal Biotechnology
Average 90 stars, based on 1 article reviews
pum1 primary antibody - by Bioz Stars, 2026-03
90/100 stars

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1) Product Images from "PUM1 knockdown prevents tumor progression by activating the PERK/eIF2/ATF4 signaling pathway in pancreatic adenocarcinoma cells"

Article Title: PUM1 knockdown prevents tumor progression by activating the PERK/eIF2/ATF4 signaling pathway in pancreatic adenocarcinoma cells

Journal: Cell Death & Disease

doi: 10.1038/s41419-019-1839-z

a PUM1 mRNA expression levels in PAAD tissues (T) and normal tissues (N) analyzed by gene expression profiling interactive analysis (GEPIA). * P < 0.05. b Analysis of the relationship between PUM1 mRNA expression and overall survival of PAAD patients analyzed using The Cancer Genome Atlas (TCGA)
Figure Legend Snippet: a PUM1 mRNA expression levels in PAAD tissues (T) and normal tissues (N) analyzed by gene expression profiling interactive analysis (GEPIA). * P < 0.05. b Analysis of the relationship between PUM1 mRNA expression and overall survival of PAAD patients analyzed using The Cancer Genome Atlas (TCGA)

Techniques Used: Expressing, Gene Expression

a Representative images of PUM1 expression by immunohistochemistry (IHC) analysis in tissue microarrays representing 60 PDAC patients. b Comparison of total scores for PUM1 assessment on tissue microarrays slides. Total score = positive staining scores × staining intensity score. * P < 0.05. c The overall survival rate of patients with PDAC was evaluated based on PUM1 expression using Kaplan–Meier analysis ( n = 60, P = 0.022)
Figure Legend Snippet: a Representative images of PUM1 expression by immunohistochemistry (IHC) analysis in tissue microarrays representing 60 PDAC patients. b Comparison of total scores for PUM1 assessment on tissue microarrays slides. Total score = positive staining scores × staining intensity score. * P < 0.05. c The overall survival rate of patients with PDAC was evaluated based on PUM1 expression using Kaplan–Meier analysis ( n = 60, P = 0.022)

Techniques Used: Expressing, Immunohistochemistry, Comparison, Staining

The relationship between  PUM1  protein levels and clinic characteristics of patients with pancreatic adenocarcinoma
Figure Legend Snippet: The relationship between PUM1 protein levels and clinic characteristics of patients with pancreatic adenocarcinoma

Techniques Used: Expressing

PUM1 mRNA ( a ) and protein ( b ) expression levels in PDAC cell lines (BxPC-3, AsPC-1, MIA PaCa-2, and PANC-1) and human pancreatic duct epithelial cells HPDE6-C7. c PUM1 expression levels in cells infected with lentivirus expressing the shRNA of PUM1 (shPUM1) or negative (NC) control empty lentivirus. d , e Effect of PUM1 knockdown on the OD values at 490 nm. f Effect of PUM1 knockdown on early apoptosis rate. b , c , f The representative graphs are on the left, and the statistical results are on the right. n = 3, * P < 0.05, for a – f
Figure Legend Snippet: PUM1 mRNA ( a ) and protein ( b ) expression levels in PDAC cell lines (BxPC-3, AsPC-1, MIA PaCa-2, and PANC-1) and human pancreatic duct epithelial cells HPDE6-C7. c PUM1 expression levels in cells infected with lentivirus expressing the shRNA of PUM1 (shPUM1) or negative (NC) control empty lentivirus. d , e Effect of PUM1 knockdown on the OD values at 490 nm. f Effect of PUM1 knockdown on early apoptosis rate. b , c , f The representative graphs are on the left, and the statistical results are on the right. n = 3, * P < 0.05, for a – f

Techniques Used: Expressing, Infection, shRNA, Control, Knockdown

Effect of PUM1 knockdown on cell migration ( a ) and invasion ( b ) detected by Transwell assays. Representative graphs (left). Bar graph showing the statistical result of migratory or invasive cells (right). c Effect of PUM1 knockdown on the expression of MMP9, VEGF, vimentin, and E-cadherin. Representative graphs of western blotting (left). Relative protein expression in reference to GAPDH (right). n = 3, * P < 0.05, for a – c
Figure Legend Snippet: Effect of PUM1 knockdown on cell migration ( a ) and invasion ( b ) detected by Transwell assays. Representative graphs (left). Bar graph showing the statistical result of migratory or invasive cells (right). c Effect of PUM1 knockdown on the expression of MMP9, VEGF, vimentin, and E-cadherin. Representative graphs of western blotting (left). Relative protein expression in reference to GAPDH (right). n = 3, * P < 0.05, for a – c

Techniques Used: Knockdown, Migration, Expressing, Western Blot

a PUM1 expression levels in tumors formed by the shPUM1 or NC group cells. b , c Effect of PUM1 knockdown on the growth of subcutaneous xenograft tumor. b Pictures of subcutaneous xenograft tumor. c Tumor growth curve. n = 8, * P < 0.05. d , e Effect of PUM1 knockdown on lung metastases examined by hematoxylin and eosin staining, or Ki67 expression detected by immunohistochemistry in the lung tissues of a lung metastasis mouse model
Figure Legend Snippet: a PUM1 expression levels in tumors formed by the shPUM1 or NC group cells. b , c Effect of PUM1 knockdown on the growth of subcutaneous xenograft tumor. b Pictures of subcutaneous xenograft tumor. c Tumor growth curve. n = 8, * P < 0.05. d , e Effect of PUM1 knockdown on lung metastases examined by hematoxylin and eosin staining, or Ki67 expression detected by immunohistochemistry in the lung tissues of a lung metastasis mouse model

Techniques Used: Expressing, Knockdown, Staining, Immunohistochemistry

Volcano plot ( a ), scatter plot ( b ), and cluster gram ( c ) of the cDNA microarrays. d Effect of PUM1 knockdown on the expression of key components of the eIF2 signaling pathway. Left: Representative graphs of western blotting. Right: Statistical result of the relative protein expression in reference to GAPDH. n = 3, * P < 0.05
Figure Legend Snippet: Volcano plot ( a ), scatter plot ( b ), and cluster gram ( c ) of the cDNA microarrays. d Effect of PUM1 knockdown on the expression of key components of the eIF2 signaling pathway. Left: Representative graphs of western blotting. Right: Statistical result of the relative protein expression in reference to GAPDH. n = 3, * P < 0.05

Techniques Used: Knockdown, Expressing, Western Blot

a Representative pictures showing p-PERK levels in 60 PDAC tissues on tissue microarray examined by immunohistochemical analysis. b Linear regression analysis showing the correlation of PUM1 and p-PERK levels in PDAC tissues ( n = 60)
Figure Legend Snippet: a Representative pictures showing p-PERK levels in 60 PDAC tissues on tissue microarray examined by immunohistochemical analysis. b Linear regression analysis showing the correlation of PUM1 and p-PERK levels in PDAC tissues ( n = 60)

Techniques Used: Microarray, Immunohistochemical staining



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Bethyl primary antibodies for pum1
Primary Antibodies For Pum1, supplied by Bethyl, 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/result/primary antibodies for pum1/product/Bethyl
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ABclonal Biotechnology pum1 primary antibody
a <t>PUM1</t> mRNA expression levels in PAAD tissues (T) and normal tissues (N) analyzed by gene expression profiling interactive analysis (GEPIA). * P < 0.05. b Analysis of the relationship between PUM1 mRNA expression and overall survival of PAAD patients analyzed using The Cancer Genome Atlas (TCGA)
Pum1 Primary Antibody, supplied by ABclonal Biotechnology, 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/result/pum1 primary antibody/product/ABclonal Biotechnology
Average 90 stars, based on 1 article reviews
pum1 primary antibody - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

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Bethyl primary anti pum1 antibody
Fig. 1. Generation of a murine <t>Pum1</t> gene trap mutation. (A) Schematic representation of the gene trap insertion into the Pum1 gene between exon 2 and exon 3. Short linear bar and black bar show the b-geo probe and Pum1 probe used for Southern blot. Exons are represented as boxes. SA, splice acceptor; b-geo, b-galactosidaseeneomycin resistance cassette. (B) Southern blot containing DNA isolated from postnatal pups of heterozygous parents. DNA was digested with SacI or SphI and hybridized with the probes shown in A (black bar). The expected fragments generated by SacI are 4.9 kb for the wild-type allele, and 7.6 kb for the mutant allele. For SphI digestion, the expected fragments are 5.6 kb for the wild-type, and 8.9 kb for the mutant allele. b-geo probe recognized a 8.9 kbp fragment when digested with SphI. (C) Characterization of Pum1 mRNA transcript. Total RNA was extracted from adult testis (T), epididymis (E) and ovary (O) of wild-type and Pum1 heterozygous mice. Two different pairs of primers were used to amplify the mutant transcript. Wild-type and mutant RTPCR products were run side by side for each sample. b-actin was used as a control. (D) PCR genotyping analysis to distinguish wild-type allele (580 bp) and mutant allele (274 bp). (E) Confirmation of Pum1- bgeo fusion protein. Testis lysates from wild-type and heterozygous mice were first blotted with anti-Pum1 antibody, and then reprobed with b-geo antibody. The Pum1 antibody can only detect one band because the 127 kDa Pum1 protein co-migrates with the 129 kDa fusion protein.
Primary Anti Pum1 Antibody, supplied by Bethyl, 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/result/primary anti pum1 antibody/product/Bethyl
Average 93 stars, based on 1 article reviews
primary anti pum1 antibody - by Bioz Stars, 2026-03
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Image Search Results


a PUM1 mRNA expression levels in PAAD tissues (T) and normal tissues (N) analyzed by gene expression profiling interactive analysis (GEPIA). * P < 0.05. b Analysis of the relationship between PUM1 mRNA expression and overall survival of PAAD patients analyzed using The Cancer Genome Atlas (TCGA)

Journal: Cell Death & Disease

Article Title: PUM1 knockdown prevents tumor progression by activating the PERK/eIF2/ATF4 signaling pathway in pancreatic adenocarcinoma cells

doi: 10.1038/s41419-019-1839-z

Figure Lengend Snippet: a PUM1 mRNA expression levels in PAAD tissues (T) and normal tissues (N) analyzed by gene expression profiling interactive analysis (GEPIA). * P < 0.05. b Analysis of the relationship between PUM1 mRNA expression and overall survival of PAAD patients analyzed using The Cancer Genome Atlas (TCGA)

Article Snippet: The PUM1 primary antibody was purchased from ABclonal Technology (Wuhan, China).

Techniques: Expressing, Gene Expression

a Representative images of PUM1 expression by immunohistochemistry (IHC) analysis in tissue microarrays representing 60 PDAC patients. b Comparison of total scores for PUM1 assessment on tissue microarrays slides. Total score = positive staining scores × staining intensity score. * P < 0.05. c The overall survival rate of patients with PDAC was evaluated based on PUM1 expression using Kaplan–Meier analysis ( n = 60, P = 0.022)

Journal: Cell Death & Disease

Article Title: PUM1 knockdown prevents tumor progression by activating the PERK/eIF2/ATF4 signaling pathway in pancreatic adenocarcinoma cells

doi: 10.1038/s41419-019-1839-z

Figure Lengend Snippet: a Representative images of PUM1 expression by immunohistochemistry (IHC) analysis in tissue microarrays representing 60 PDAC patients. b Comparison of total scores for PUM1 assessment on tissue microarrays slides. Total score = positive staining scores × staining intensity score. * P < 0.05. c The overall survival rate of patients with PDAC was evaluated based on PUM1 expression using Kaplan–Meier analysis ( n = 60, P = 0.022)

Article Snippet: The PUM1 primary antibody was purchased from ABclonal Technology (Wuhan, China).

Techniques: Expressing, Immunohistochemistry, Comparison, Staining

The relationship between  PUM1  protein levels and clinic characteristics of patients with pancreatic adenocarcinoma

Journal: Cell Death & Disease

Article Title: PUM1 knockdown prevents tumor progression by activating the PERK/eIF2/ATF4 signaling pathway in pancreatic adenocarcinoma cells

doi: 10.1038/s41419-019-1839-z

Figure Lengend Snippet: The relationship between PUM1 protein levels and clinic characteristics of patients with pancreatic adenocarcinoma

Article Snippet: The PUM1 primary antibody was purchased from ABclonal Technology (Wuhan, China).

Techniques: Expressing

PUM1 mRNA ( a ) and protein ( b ) expression levels in PDAC cell lines (BxPC-3, AsPC-1, MIA PaCa-2, and PANC-1) and human pancreatic duct epithelial cells HPDE6-C7. c PUM1 expression levels in cells infected with lentivirus expressing the shRNA of PUM1 (shPUM1) or negative (NC) control empty lentivirus. d , e Effect of PUM1 knockdown on the OD values at 490 nm. f Effect of PUM1 knockdown on early apoptosis rate. b , c , f The representative graphs are on the left, and the statistical results are on the right. n = 3, * P < 0.05, for a – f

Journal: Cell Death & Disease

Article Title: PUM1 knockdown prevents tumor progression by activating the PERK/eIF2/ATF4 signaling pathway in pancreatic adenocarcinoma cells

doi: 10.1038/s41419-019-1839-z

Figure Lengend Snippet: PUM1 mRNA ( a ) and protein ( b ) expression levels in PDAC cell lines (BxPC-3, AsPC-1, MIA PaCa-2, and PANC-1) and human pancreatic duct epithelial cells HPDE6-C7. c PUM1 expression levels in cells infected with lentivirus expressing the shRNA of PUM1 (shPUM1) or negative (NC) control empty lentivirus. d , e Effect of PUM1 knockdown on the OD values at 490 nm. f Effect of PUM1 knockdown on early apoptosis rate. b , c , f The representative graphs are on the left, and the statistical results are on the right. n = 3, * P < 0.05, for a – f

Article Snippet: The PUM1 primary antibody was purchased from ABclonal Technology (Wuhan, China).

Techniques: Expressing, Infection, shRNA, Control, Knockdown

Effect of PUM1 knockdown on cell migration ( a ) and invasion ( b ) detected by Transwell assays. Representative graphs (left). Bar graph showing the statistical result of migratory or invasive cells (right). c Effect of PUM1 knockdown on the expression of MMP9, VEGF, vimentin, and E-cadherin. Representative graphs of western blotting (left). Relative protein expression in reference to GAPDH (right). n = 3, * P < 0.05, for a – c

Journal: Cell Death & Disease

Article Title: PUM1 knockdown prevents tumor progression by activating the PERK/eIF2/ATF4 signaling pathway in pancreatic adenocarcinoma cells

doi: 10.1038/s41419-019-1839-z

Figure Lengend Snippet: Effect of PUM1 knockdown on cell migration ( a ) and invasion ( b ) detected by Transwell assays. Representative graphs (left). Bar graph showing the statistical result of migratory or invasive cells (right). c Effect of PUM1 knockdown on the expression of MMP9, VEGF, vimentin, and E-cadherin. Representative graphs of western blotting (left). Relative protein expression in reference to GAPDH (right). n = 3, * P < 0.05, for a – c

Article Snippet: The PUM1 primary antibody was purchased from ABclonal Technology (Wuhan, China).

Techniques: Knockdown, Migration, Expressing, Western Blot

a PUM1 expression levels in tumors formed by the shPUM1 or NC group cells. b , c Effect of PUM1 knockdown on the growth of subcutaneous xenograft tumor. b Pictures of subcutaneous xenograft tumor. c Tumor growth curve. n = 8, * P < 0.05. d , e Effect of PUM1 knockdown on lung metastases examined by hematoxylin and eosin staining, or Ki67 expression detected by immunohistochemistry in the lung tissues of a lung metastasis mouse model

Journal: Cell Death & Disease

Article Title: PUM1 knockdown prevents tumor progression by activating the PERK/eIF2/ATF4 signaling pathway in pancreatic adenocarcinoma cells

doi: 10.1038/s41419-019-1839-z

Figure Lengend Snippet: a PUM1 expression levels in tumors formed by the shPUM1 or NC group cells. b , c Effect of PUM1 knockdown on the growth of subcutaneous xenograft tumor. b Pictures of subcutaneous xenograft tumor. c Tumor growth curve. n = 8, * P < 0.05. d , e Effect of PUM1 knockdown on lung metastases examined by hematoxylin and eosin staining, or Ki67 expression detected by immunohistochemistry in the lung tissues of a lung metastasis mouse model

Article Snippet: The PUM1 primary antibody was purchased from ABclonal Technology (Wuhan, China).

Techniques: Expressing, Knockdown, Staining, Immunohistochemistry

Volcano plot ( a ), scatter plot ( b ), and cluster gram ( c ) of the cDNA microarrays. d Effect of PUM1 knockdown on the expression of key components of the eIF2 signaling pathway. Left: Representative graphs of western blotting. Right: Statistical result of the relative protein expression in reference to GAPDH. n = 3, * P < 0.05

Journal: Cell Death & Disease

Article Title: PUM1 knockdown prevents tumor progression by activating the PERK/eIF2/ATF4 signaling pathway in pancreatic adenocarcinoma cells

doi: 10.1038/s41419-019-1839-z

Figure Lengend Snippet: Volcano plot ( a ), scatter plot ( b ), and cluster gram ( c ) of the cDNA microarrays. d Effect of PUM1 knockdown on the expression of key components of the eIF2 signaling pathway. Left: Representative graphs of western blotting. Right: Statistical result of the relative protein expression in reference to GAPDH. n = 3, * P < 0.05

Article Snippet: The PUM1 primary antibody was purchased from ABclonal Technology (Wuhan, China).

Techniques: Knockdown, Expressing, Western Blot

a Representative pictures showing p-PERK levels in 60 PDAC tissues on tissue microarray examined by immunohistochemical analysis. b Linear regression analysis showing the correlation of PUM1 and p-PERK levels in PDAC tissues ( n = 60)

Journal: Cell Death & Disease

Article Title: PUM1 knockdown prevents tumor progression by activating the PERK/eIF2/ATF4 signaling pathway in pancreatic adenocarcinoma cells

doi: 10.1038/s41419-019-1839-z

Figure Lengend Snippet: a Representative pictures showing p-PERK levels in 60 PDAC tissues on tissue microarray examined by immunohistochemical analysis. b Linear regression analysis showing the correlation of PUM1 and p-PERK levels in PDAC tissues ( n = 60)

Article Snippet: The PUM1 primary antibody was purchased from ABclonal Technology (Wuhan, China).

Techniques: Microarray, Immunohistochemical staining

Fig. 1. Generation of a murine Pum1 gene trap mutation. (A) Schematic representation of the gene trap insertion into the Pum1 gene between exon 2 and exon 3. Short linear bar and black bar show the b-geo probe and Pum1 probe used for Southern blot. Exons are represented as boxes. SA, splice acceptor; b-geo, b-galactosidaseeneomycin resistance cassette. (B) Southern blot containing DNA isolated from postnatal pups of heterozygous parents. DNA was digested with SacI or SphI and hybridized with the probes shown in A (black bar). The expected fragments generated by SacI are 4.9 kb for the wild-type allele, and 7.6 kb for the mutant allele. For SphI digestion, the expected fragments are 5.6 kb for the wild-type, and 8.9 kb for the mutant allele. b-geo probe recognized a 8.9 kbp fragment when digested with SphI. (C) Characterization of Pum1 mRNA transcript. Total RNA was extracted from adult testis (T), epididymis (E) and ovary (O) of wild-type and Pum1 heterozygous mice. Two different pairs of primers were used to amplify the mutant transcript. Wild-type and mutant RTPCR products were run side by side for each sample. b-actin was used as a control. (D) PCR genotyping analysis to distinguish wild-type allele (580 bp) and mutant allele (274 bp). (E) Confirmation of Pum1- bgeo fusion protein. Testis lysates from wild-type and heterozygous mice were first blotted with anti-Pum1 antibody, and then reprobed with b-geo antibody. The Pum1 antibody can only detect one band because the 127 kDa Pum1 protein co-migrates with the 129 kDa fusion protein.

Journal: Biochemical and biophysical research communications

Article Title: Loss of preimplantation embryo resulting from a Pum1 gene trap mutation.

doi: 10.1016/j.bbrc.2015.04.019

Figure Lengend Snippet: Fig. 1. Generation of a murine Pum1 gene trap mutation. (A) Schematic representation of the gene trap insertion into the Pum1 gene between exon 2 and exon 3. Short linear bar and black bar show the b-geo probe and Pum1 probe used for Southern blot. Exons are represented as boxes. SA, splice acceptor; b-geo, b-galactosidaseeneomycin resistance cassette. (B) Southern blot containing DNA isolated from postnatal pups of heterozygous parents. DNA was digested with SacI or SphI and hybridized with the probes shown in A (black bar). The expected fragments generated by SacI are 4.9 kb for the wild-type allele, and 7.6 kb for the mutant allele. For SphI digestion, the expected fragments are 5.6 kb for the wild-type, and 8.9 kb for the mutant allele. b-geo probe recognized a 8.9 kbp fragment when digested with SphI. (C) Characterization of Pum1 mRNA transcript. Total RNA was extracted from adult testis (T), epididymis (E) and ovary (O) of wild-type and Pum1 heterozygous mice. Two different pairs of primers were used to amplify the mutant transcript. Wild-type and mutant RTPCR products were run side by side for each sample. b-actin was used as a control. (D) PCR genotyping analysis to distinguish wild-type allele (580 bp) and mutant allele (274 bp). (E) Confirmation of Pum1- bgeo fusion protein. Testis lysates from wild-type and heterozygous mice were first blotted with anti-Pum1 antibody, and then reprobed with b-geo antibody. The Pum1 antibody can only detect one band because the 127 kDa Pum1 protein co-migrates with the 129 kDa fusion protein.

Article Snippet: The blots were incubated in a 1:2000 dilution of the Primary anti-Pum1 antibody (Bethyl Lab) at 4 C overnight.

Techniques: Mutagenesis, Southern Blot, Isolation, Generated, Reverse Transcription Polymerase Chain Reaction, Control