Review




Structured Review

Asterand Inc sum149 cell line
Sum149 Cell Line, supplied by Asterand 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/sum149+cell+line/sum149+cells/bio_rxiv__2025__06__18__660428-200-0-7
Average 90 stars, based on 1 article reviews
sum149 cell line - by Bioz Stars, 2026-09
90/100 stars

Images

Related Articles

Cell Culture:

Article Title: NDR1 increases NOTCH1 signaling activity by impairing Fbw7 mediated NICD degradation to enhance breast cancer stem cell properties
Article Snippet: MCF-7 cells were obtained from the ATCC and were cultured in DMEM (Thermo Fisher Scientific) supplemented with 10% fetal bovine serum (Thermo Fisher Scientific). .. SUM149 cell line was obtained from Asterand and was cultured in Ham's F-12 supplemented with 5% fetal bovine serum. ..

Article Title: Lipocalin 2 promotes inflammatory breast cancer tumorigenesis and skin invasion
Article Snippet: .. The SUM149 cell line was purchased from Asterand (Detroit, MI, USA), and MDA‐IBC3 cell line was generated in Dr. Woodward's laboratory [ , ] and cultured in Ham's F‐12 media supplemented with 10% FBS (GIBCO, Thermo Fisher, Carlsbad, CA, USA), 1 μg·mL −1 hydrocortisone (#H0888, Sigma‐Aldrich, St. Louis, MO, USA), 5 μg·mL −1 insulin (#12585014; Thermo Fisher), and 1% antibiotic‐antimycotic (#15240062; Thermo Fisher). .. HEK293T cells were purchased from the American Type Culture Collection (Manassas, VA, USA) and cultured in Dulbecco's modified Eagle's medium supplemented with 10% FBS and 1% penicillin and streptomycin (#15140122; Invitrogen, Carlsbad, CA, USA).

other:

Article Title: Sulforaphene Interferes with Human Breast Cancer Cell Migration and Invasion through Inhibition of Hedgehog Signaling.
Article Snippet: Journal of Agricultural and Food Chemistry is published by the American Chemical Society.. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society.. Copyright © American Chemical Society.

Article Title: Pharmacological targeting of GLI1 inhibits proliferation, tumor emboli formation and in vivo tumor growth of inflammatory breast cancer cells
Article Snippet: The SUM149, SUM159 and SUM190 cell lines were obtained from Asterand Inc (Detroit, MI) and cultured per manufacturer’s instructions and as described previously [35].

Article Title: Preferential Inhibition of Wnt/β-Catenin Signaling by Novel Benzimidazole Compounds in Triple-Negative Breast Cancer
Article Snippet: SUM149 and SUM159 cell lines were purchased from Asterand (Detroit, MI, USA) and cultured in DMEM/F12 with 5% FBS, hydrocortisone and insulin.

Article Title: Soluble E-cadherin Drives Brain Metastasis in Inflammatory Breast Cancer
Article Snippet: SUM149,and SUM190 cell line was purchased from Asterand (Detroit, MI), and the MDA-IBC3 cell line was generated in the laboratory of Dr. Wendy Woodward at MD Anderson., The human TNBC cell line BCX010, derived from a patient with triple-negative inflammatory breast cancer, was generously donated by Dr. Funda Meric-Bernstam (MD Anderson Cancer Center) .The cell culture conditions were described previously., HEK293T cells were obtained from the American Type Culture Collection (Manassas, VA, USA) and were cultured in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% FBS and 1% penicillin and streptomycin (#15140122, Invitrogen, Carlsbad, CA, USA) at 37oC in a humidified incubator with 5% CO2.

Article Title: Cyclin E overexpression as a biomarker for combination treatment strategies in inflammatory breast cancer
Article Snippet: Cell culture conditions SUM149 and SUM185 cell lines were obtained from Asterand, KPL4 cells were obtained from Naoto Ueno (MD Anderson), and the remaining cell lines were purchased from American Type Culture Collection (ATCC).

Article Title: Photothermal ablation of inflammatory breast cancer tumor emboli using plasmonic gold nanostars
Article Snippet: SUM149 (inflammatory ductal carcinoma) and SUM190 (primary human inflammatory luminal breast carcinoma) cell lines were obtained from Asterand, Inc., and cultured as previously described. rSUM149 cells, which exhibit multidrug resistance, were synthesized in our laboratory from SUM149 cells and cultured in a manner similar to SUM149 cells with 7.5 μM GW583340 (Sigma-Aldrich, St Louis, MO, USA) added a day after splitting for each passage as described previously., BT474M1 (invasive ductal carcinoma) provided by Dr Timothy Clay at Duke University, was cultured in Dulbecco’s Modified Eagle’s Medium/F12 (Sigma-Aldrich) supplemented with 10% fetal bovine serum (Sigma-Aldrich) and 1% penicillin/streptomycin.

Multiple Displacement Amplification:

Article Title: Lipocalin 2 promotes inflammatory breast cancer tumorigenesis and skin invasion
Article Snippet: .. The SUM149 cell line was purchased from Asterand (Detroit, MI, USA), and MDA‐IBC3 cell line was generated in Dr. Woodward's laboratory [ , ] and cultured in Ham's F‐12 media supplemented with 10% FBS (GIBCO, Thermo Fisher, Carlsbad, CA, USA), 1 μg·mL −1 hydrocortisone (#H0888, Sigma‐Aldrich, St. Louis, MO, USA), 5 μg·mL −1 insulin (#12585014; Thermo Fisher), and 1% antibiotic‐antimycotic (#15240062; Thermo Fisher). .. HEK293T cells were purchased from the American Type Culture Collection (Manassas, VA, USA) and cultured in Dulbecco's modified Eagle's medium supplemented with 10% FBS and 1% penicillin and streptomycin (#15140122; Invitrogen, Carlsbad, CA, USA).

Generated:

Article Title: Lipocalin 2 promotes inflammatory breast cancer tumorigenesis and skin invasion
Article Snippet: .. The SUM149 cell line was purchased from Asterand (Detroit, MI, USA), and MDA‐IBC3 cell line was generated in Dr. Woodward's laboratory [ , ] and cultured in Ham's F‐12 media supplemented with 10% FBS (GIBCO, Thermo Fisher, Carlsbad, CA, USA), 1 μg·mL −1 hydrocortisone (#H0888, Sigma‐Aldrich, St. Louis, MO, USA), 5 μg·mL −1 insulin (#12585014; Thermo Fisher), and 1% antibiotic‐antimycotic (#15240062; Thermo Fisher). .. HEK293T cells were purchased from the American Type Culture Collection (Manassas, VA, USA) and cultured in Dulbecco's modified Eagle's medium supplemented with 10% FBS and 1% penicillin and streptomycin (#15140122; Invitrogen, Carlsbad, CA, USA).



Similar Products

90
Asterand Inc sum149 cell line
Sum149 Cell Line, supplied by Asterand 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/sum149+cell+line/sum149+cells/bio_rxiv__2025__06__18__660428-200-0-7
Average 90 stars, based on 1 article reviews
sum149 cell line - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier

90
Asterand Inc human ibc cell line sum149
Human Ibc Cell Line Sum149, supplied by Asterand 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/sum149+cell+line/sum149+cells/pm40329335-66-1-9
Average 90 stars, based on 1 article reviews
human ibc cell line sum149 - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier

90
Asterand Inc human breast cancer cell lines sum52, sum102, sum149, sum159, and sum229
Human Breast Cancer Cell Lines Sum52, Sum102, Sum149, Sum159, And Sum229, supplied by Asterand 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/sum149+cell+line/sum149+cells/pmc11121248-157-11-15
Average 90 stars, based on 1 article reviews
human breast cancer cell lines sum52, sum102, sum149, sum159, and sum229 - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier

90
BioIVT Inc cell line ( homo sapiens ) , sum149
( a ) Expression of DDI2 in the CRISPR-generated clones of HAP1 cells used in this work was analyzed by western blot. ( b ) The experimental setup used in this study. Cells were pulse treated with bortezomib (Btz) or carfilzomib (Cfz) for 1 hr, then cultured in drug-free media for times indicated and analyzed as described. ( c ) The viability of wt- and DDI2 KO clones of HAP1 cells was measured using CellTiter-Glo, and the inhibition of β5 sites was measured with the Proteasome-Glo assay at times indicated; n=2–5. ( d ) Knockout of DDI2 inhibits the Nrf1 processing. Western blots of Btz-treated HAP1 cells. The sample in the first lane is wt cells treated with VCP/p97 inhibitor CB-5083 immediately after removal of Btz. VCP inhibitors blocks Nrf1 processing ( ; ; ). ( e ) MDA-MB-231 and <t>SUM149</t> cells were analyzed by western blot 72 hr after transfection with DDI2 siRNAs ( f ) Theβ5 activity in siRNA-transfected SUM149 and MDA-MB-231 was measured using Suc-LLVY-AMC immediately and 18 hr after treatment with 100 nM Btz; n=3. ( g ) β5 activity was measured in HCT-116 cells with the Proteasome-Glo assay immediately and 18 hr after treatment with PIs; n=2. Figure 1—source data 1. PDF file containing and original full-size western blot membranes (anti-DDI2, anti-GAPDH) with molecular weight markers. Figure 1—source data 2. Excel file containing data for . Figure 1—source data 3. PDF file containing and original full-size western blot membranes (anti-Nrf1, anti-DDI2, anti-β-actin) with molecular weight markers. Figure 1—source data 4. PDF file containing and full-size western blot membranes (anti-DDI2, anti-β-actin). Additional lanes demonstrate that the knockdown of DDI2 is maintained throughout the experiment. Figure 1—source data 5. Excel file containing data and statistical analysis for . Figure 1—source data 6. Excel file containing data for .
Cell Line ( Homo Sapiens ) , Sum149, supplied by BioIVT 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/sum149+cell+line/sum149/pmc11018354-5-7-9
Average 90 stars, based on 1 article reviews
cell line ( homo sapiens ) , sum149 - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier

90
Johns Hopkins HealthCare sum149 cell line
( a ) Expression of DDI2 in the CRISPR-generated clones of HAP1 cells used in this work was analyzed by western blot. ( b ) The experimental setup used in this study. Cells were pulse treated with bortezomib (Btz) or carfilzomib (Cfz) for 1 hr, then cultured in drug-free media for times indicated and analyzed as described. ( c ) The viability of wt- and DDI2 KO clones of HAP1 cells was measured using CellTiter-Glo, and the inhibition of β5 sites was measured with the Proteasome-Glo assay at times indicated; n=2–5. ( d ) Knockout of DDI2 inhibits the Nrf1 processing. Western blots of Btz-treated HAP1 cells. The sample in the first lane is wt cells treated with VCP/p97 inhibitor CB-5083 immediately after removal of Btz. VCP inhibitors blocks Nrf1 processing ( ; ; ). ( e ) MDA-MB-231 and <t>SUM149</t> cells were analyzed by western blot 72 hr after transfection with DDI2 siRNAs ( f ) Theβ5 activity in siRNA-transfected SUM149 and MDA-MB-231 was measured using Suc-LLVY-AMC immediately and 18 hr after treatment with 100 nM Btz; n=3. ( g ) β5 activity was measured in HCT-116 cells with the Proteasome-Glo assay immediately and 18 hr after treatment with PIs; n=2. Figure 1—source data 1. PDF file containing and original full-size western blot membranes (anti-DDI2, anti-GAPDH) with molecular weight markers. Figure 1—source data 2. Excel file containing data for . Figure 1—source data 3. PDF file containing and original full-size western blot membranes (anti-Nrf1, anti-DDI2, anti-β-actin) with molecular weight markers. Figure 1—source data 4. PDF file containing and full-size western blot membranes (anti-DDI2, anti-β-actin). Additional lanes demonstrate that the knockdown of DDI2 is maintained throughout the experiment. Figure 1—source data 5. Excel file containing data and statistical analysis for . Figure 1—source data 6. Excel file containing data for .
Sum149 Cell Line, 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/sum149+cell+line/sum159+cells/us11607466-391-1-24
Average 90 stars, based on 1 article reviews
sum149 cell line - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier

90
BioIVT Inc human ibc cell line sum149
( a ) Expression of DDI2 in the CRISPR-generated clones of HAP1 cells used in this work was analyzed by western blot. ( b ) The experimental setup used in this study. Cells were pulse treated with bortezomib (Btz) or carfilzomib (Cfz) for 1 hr, then cultured in drug-free media for times indicated and analyzed as described. ( c ) The viability of wt- and DDI2 KO clones of HAP1 cells was measured using CellTiter-Glo, and the inhibition of β5 sites was measured with the Proteasome-Glo assay at times indicated; n=2–5. ( d ) Knockout of DDI2 inhibits the Nrf1 processing. Western blots of Btz-treated HAP1 cells. The sample in the first lane is wt cells treated with VCP/p97 inhibitor CB-5083 immediately after removal of Btz. VCP inhibitors blocks Nrf1 processing ( ; ; ). ( e ) MDA-MB-231 and <t>SUM149</t> cells were analyzed by western blot 72 hr after transfection with DDI2 siRNAs ( f ) Theβ5 activity in siRNA-transfected SUM149 and MDA-MB-231 was measured using Suc-LLVY-AMC immediately and 18 hr after treatment with 100 nM Btz; n=3. ( g ) β5 activity was measured in HCT-116 cells with the Proteasome-Glo assay immediately and 18 hr after treatment with PIs; n=2. Figure 1—source data 1. PDF file containing and original full-size western blot membranes (anti-DDI2, anti-GAPDH) with molecular weight markers. Figure 1—source data 2. Excel file containing data for . Figure 1—source data 3. PDF file containing and original full-size western blot membranes (anti-Nrf1, anti-DDI2, anti-β-actin) with molecular weight markers. Figure 1—source data 4. PDF file containing and full-size western blot membranes (anti-DDI2, anti-β-actin). Additional lanes demonstrate that the knockdown of DDI2 is maintained throughout the experiment. Figure 1—source data 5. Excel file containing data and statistical analysis for . Figure 1—source data 6. Excel file containing data for .
Human Ibc Cell Line Sum149, supplied by BioIVT 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/sum149+cell+line/sum149/pm36525493-214-0-8
Average 90 stars, based on 1 article reviews
human ibc cell line sum149 - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier

90
BioIVT Inc sum149 tnbc cell line
( a ) Expression of DDI2 in the CRISPR-generated clones of HAP1 cells used in this work was analyzed by western blot. ( b ) The experimental setup used in this study. Cells were pulse treated with bortezomib (Btz) or carfilzomib (Cfz) for 1 hr, then cultured in drug-free media for times indicated and analyzed as described. ( c ) The viability of wt- and DDI2 KO clones of HAP1 cells was measured using CellTiter-Glo, and the inhibition of β5 sites was measured with the Proteasome-Glo assay at times indicated; n=2–5. ( d ) Knockout of DDI2 inhibits the Nrf1 processing. Western blots of Btz-treated HAP1 cells. The sample in the first lane is wt cells treated with VCP/p97 inhibitor CB-5083 immediately after removal of Btz. VCP inhibitors blocks Nrf1 processing ( ; ; ). ( e ) MDA-MB-231 and <t>SUM149</t> cells were analyzed by western blot 72 hr after transfection with DDI2 siRNAs ( f ) Theβ5 activity in siRNA-transfected SUM149 and MDA-MB-231 was measured using Suc-LLVY-AMC immediately and 18 hr after treatment with 100 nM Btz; n=3. ( g ) β5 activity was measured in HCT-116 cells with the Proteasome-Glo assay immediately and 18 hr after treatment with PIs; n=2. Figure 1—source data 1. PDF file containing and original full-size western blot membranes (anti-DDI2, anti-GAPDH) with molecular weight markers. Figure 1—source data 2. Excel file containing data for . Figure 1—source data 3. PDF file containing and original full-size western blot membranes (anti-Nrf1, anti-DDI2, anti-β-actin) with molecular weight markers. Figure 1—source data 4. PDF file containing and full-size western blot membranes (anti-DDI2, anti-β-actin). Additional lanes demonstrate that the knockdown of DDI2 is maintained throughout the experiment. Figure 1—source data 5. Excel file containing data and statistical analysis for . Figure 1—source data 6. Excel file containing data for .
Sum149 Tnbc Cell Line, supplied by BioIVT 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/sum149+cell+line/sum149/pm36253486-548-1-11
Average 90 stars, based on 1 article reviews
sum149 tnbc cell line - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier

Image Search Results


( a ) Expression of DDI2 in the CRISPR-generated clones of HAP1 cells used in this work was analyzed by western blot. ( b ) The experimental setup used in this study. Cells were pulse treated with bortezomib (Btz) or carfilzomib (Cfz) for 1 hr, then cultured in drug-free media for times indicated and analyzed as described. ( c ) The viability of wt- and DDI2 KO clones of HAP1 cells was measured using CellTiter-Glo, and the inhibition of β5 sites was measured with the Proteasome-Glo assay at times indicated; n=2–5. ( d ) Knockout of DDI2 inhibits the Nrf1 processing. Western blots of Btz-treated HAP1 cells. The sample in the first lane is wt cells treated with VCP/p97 inhibitor CB-5083 immediately after removal of Btz. VCP inhibitors blocks Nrf1 processing ( ; ; ). ( e ) MDA-MB-231 and SUM149 cells were analyzed by western blot 72 hr after transfection with DDI2 siRNAs ( f ) Theβ5 activity in siRNA-transfected SUM149 and MDA-MB-231 was measured using Suc-LLVY-AMC immediately and 18 hr after treatment with 100 nM Btz; n=3. ( g ) β5 activity was measured in HCT-116 cells with the Proteasome-Glo assay immediately and 18 hr after treatment with PIs; n=2. Figure 1—source data 1. PDF file containing and original full-size western blot membranes (anti-DDI2, anti-GAPDH) with molecular weight markers. Figure 1—source data 2. Excel file containing data for . Figure 1—source data 3. PDF file containing and original full-size western blot membranes (anti-Nrf1, anti-DDI2, anti-β-actin) with molecular weight markers. Figure 1—source data 4. PDF file containing and full-size western blot membranes (anti-DDI2, anti-β-actin). Additional lanes demonstrate that the knockdown of DDI2 is maintained throughout the experiment. Figure 1—source data 5. Excel file containing data and statistical analysis for . Figure 1—source data 6. Excel file containing data for .

Journal: eLife

Article Title: Early recovery of proteasome activity in cells pulse-treated with proteasome inhibitors is independent of DDI2

doi: 10.7554/eLife.91678

Figure Lengend Snippet: ( a ) Expression of DDI2 in the CRISPR-generated clones of HAP1 cells used in this work was analyzed by western blot. ( b ) The experimental setup used in this study. Cells were pulse treated with bortezomib (Btz) or carfilzomib (Cfz) for 1 hr, then cultured in drug-free media for times indicated and analyzed as described. ( c ) The viability of wt- and DDI2 KO clones of HAP1 cells was measured using CellTiter-Glo, and the inhibition of β5 sites was measured with the Proteasome-Glo assay at times indicated; n=2–5. ( d ) Knockout of DDI2 inhibits the Nrf1 processing. Western blots of Btz-treated HAP1 cells. The sample in the first lane is wt cells treated with VCP/p97 inhibitor CB-5083 immediately after removal of Btz. VCP inhibitors blocks Nrf1 processing ( ; ; ). ( e ) MDA-MB-231 and SUM149 cells were analyzed by western blot 72 hr after transfection with DDI2 siRNAs ( f ) Theβ5 activity in siRNA-transfected SUM149 and MDA-MB-231 was measured using Suc-LLVY-AMC immediately and 18 hr after treatment with 100 nM Btz; n=3. ( g ) β5 activity was measured in HCT-116 cells with the Proteasome-Glo assay immediately and 18 hr after treatment with PIs; n=2. Figure 1—source data 1. PDF file containing and original full-size western blot membranes (anti-DDI2, anti-GAPDH) with molecular weight markers. Figure 1—source data 2. Excel file containing data for . Figure 1—source data 3. PDF file containing and original full-size western blot membranes (anti-Nrf1, anti-DDI2, anti-β-actin) with molecular weight markers. Figure 1—source data 4. PDF file containing and full-size western blot membranes (anti-DDI2, anti-β-actin). Additional lanes demonstrate that the knockdown of DDI2 is maintained throughout the experiment. Figure 1—source data 5. Excel file containing data and statistical analysis for . Figure 1—source data 6. Excel file containing data for .

Article Snippet: Cell line ( Homo sapiens ) , SUM149 , BioIVT , RRID: CVCL_3422 , .

Techniques: Expressing, CRISPR, Generated, Clone Assay, Western Blot, Cell Culture, Inhibition, Glo Assay, Knock-Out, Transfection, Activity Assay, Molecular Weight, Knockdown

( a ) Cells were treated with PIs for 1 hr, media was shaken off, and cells were cultured in an inhibitor-free fresh media for 48 hr when Alamar Blue assay was performed; n=3–4. See Figure 1 in for a comparison of SUM149 and MDA-MB-231 cells. ( b ) The β5 proteasome activity was measured using Suc-LLVY-AMC in the cell extracts of untreated cells; n=2-8. Figure 1—figure supplement 2—source data 1. Excel file containing data for both panels.

Journal: eLife

Article Title: Early recovery of proteasome activity in cells pulse-treated with proteasome inhibitors is independent of DDI2

doi: 10.7554/eLife.91678

Figure Lengend Snippet: ( a ) Cells were treated with PIs for 1 hr, media was shaken off, and cells were cultured in an inhibitor-free fresh media for 48 hr when Alamar Blue assay was performed; n=3–4. See Figure 1 in for a comparison of SUM149 and MDA-MB-231 cells. ( b ) The β5 proteasome activity was measured using Suc-LLVY-AMC in the cell extracts of untreated cells; n=2-8. Figure 1—figure supplement 2—source data 1. Excel file containing data for both panels.

Article Snippet: Cell line ( Homo sapiens ) , SUM149 , BioIVT , RRID: CVCL_3422 , .

Techniques: Cell Culture, Alamar Blue Assay, Comparison, Activity Assay

Journal: eLife

Article Title: Early recovery of proteasome activity in cells pulse-treated with proteasome inhibitors is independent of DDI2

doi: 10.7554/eLife.91678

Figure Lengend Snippet:

Article Snippet: Cell line ( Homo sapiens ) , SUM149 , BioIVT , RRID: CVCL_3422 , .

Techniques: Generated, CRISPR, Mutagenesis, Transfection, Construct, Sequencing, Bradford Assay, Isolation, Reverse Transcription, SYBR Green Assay, Viability Assay, Software