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negative control scrambled sirna  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology negative control scrambled sirna
    Relationship between MIF and TMED10. (A) Secretion of MIF was measured in HEK293T cells either untreated or treated with brefeldin A. (B) Secretion of MIF was measured in HEK293T cells untreated or treated with the indicated doses of probenecid. (C) GST or the indicated GST-TMED10 domains coupled to glutathione sepharose beads were incubated with whole cell lysates from HEK293T cells expressing Flag-MIF. Elutes were subjected to SDS-PAGE and immunoblotted with an anti-Flag antibody. (D) GST-MIF coupled to glutathione sepharose beads was incubated with whole cell lysate from HEK293T cells expressing GFP-TMED10 or GFP-TMED10(ΔCT). Elutes were subjected to SDS-PAGE and immunoblotted with anti-GFP antibody. (E) Secretion of MIF was measured in HEK293T cells expressing mock or GFP-TMED10. (F) Secretion of MIF was measured in HEK293T cells treated with control <t>siRNA</t> or siRNA targeting TMED10 for 72 h. (G) A crosslink assay was performed in HEK293T cells expressing GFP-TMED10 with mock or Flag-MIF to examine the oligomeric form of TMED10. (H) Secretion of Flag-MIF was measured in HEK293T cells expressing mock, RAB1A, 1B, and 2A.
    Negative Control Scrambled Sirna, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 6363 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Images

    1) Product Images from "TRPML3 and TRPML1/3 differentially regulate unconventional MIF secretion through TMED10 and secretory autophagy"

    Article Title: TRPML3 and TRPML1/3 differentially regulate unconventional MIF secretion through TMED10 and secretory autophagy

    Journal: Autophagy Reports

    doi: 10.1080/27694127.2026.2740425

    Relationship between MIF and TMED10. (A) Secretion of MIF was measured in HEK293T cells either untreated or treated with brefeldin A. (B) Secretion of MIF was measured in HEK293T cells untreated or treated with the indicated doses of probenecid. (C) GST or the indicated GST-TMED10 domains coupled to glutathione sepharose beads were incubated with whole cell lysates from HEK293T cells expressing Flag-MIF. Elutes were subjected to SDS-PAGE and immunoblotted with an anti-Flag antibody. (D) GST-MIF coupled to glutathione sepharose beads was incubated with whole cell lysate from HEK293T cells expressing GFP-TMED10 or GFP-TMED10(ΔCT). Elutes were subjected to SDS-PAGE and immunoblotted with anti-GFP antibody. (E) Secretion of MIF was measured in HEK293T cells expressing mock or GFP-TMED10. (F) Secretion of MIF was measured in HEK293T cells treated with control siRNA or siRNA targeting TMED10 for 72 h. (G) A crosslink assay was performed in HEK293T cells expressing GFP-TMED10 with mock or Flag-MIF to examine the oligomeric form of TMED10. (H) Secretion of Flag-MIF was measured in HEK293T cells expressing mock, RAB1A, 1B, and 2A.
    Figure Legend Snippet: Relationship between MIF and TMED10. (A) Secretion of MIF was measured in HEK293T cells either untreated or treated with brefeldin A. (B) Secretion of MIF was measured in HEK293T cells untreated or treated with the indicated doses of probenecid. (C) GST or the indicated GST-TMED10 domains coupled to glutathione sepharose beads were incubated with whole cell lysates from HEK293T cells expressing Flag-MIF. Elutes were subjected to SDS-PAGE and immunoblotted with an anti-Flag antibody. (D) GST-MIF coupled to glutathione sepharose beads was incubated with whole cell lysate from HEK293T cells expressing GFP-TMED10 or GFP-TMED10(ΔCT). Elutes were subjected to SDS-PAGE and immunoblotted with anti-GFP antibody. (E) Secretion of MIF was measured in HEK293T cells expressing mock or GFP-TMED10. (F) Secretion of MIF was measured in HEK293T cells treated with control siRNA or siRNA targeting TMED10 for 72 h. (G) A crosslink assay was performed in HEK293T cells expressing GFP-TMED10 with mock or Flag-MIF to examine the oligomeric form of TMED10. (H) Secretion of Flag-MIF was measured in HEK293T cells expressing mock, RAB1A, 1B, and 2A.

    Techniques Used: Incubation, Expressing, SDS Page, Control

    Effect of autophagy on MIF secretion. (A) HeLa cells expressing GFP-LC3 and mCherry-MIF were treated with cold digitonin (50 µg/ml) and imaged by fluorescence microscopy. (B) Secretion of MIF was measured in HEK293T cells either untreated or treated with 10 μM SAR405. (C) Secretion of MIF was measured in HEK293T cells treated with control siRNA or siRNA targeting ATG5 for 72 h. (D) Secretion of MIF was measured in HEK293T cells either untreated or treated with 100 nM bafilomycin A1. (E) Secretion of MIF was measured in HEK293T cells treated with control siRNA or siRNA targeting SYT5 for 48 h. Knockdown efficiency was confirmed by immunoblotting for SYT5. (F) Secretion of Flag-MIF was measured in HEK293T cells expressing mock or GFP-SEC22B. (G) HeLa cells expressing GFP-SEC22B and mCherry-MIF were treated with cold digitonin (50 µg/ml) and imaged by fluorescence microscopy. (H, upper) HeLa cells co-expressing GFP-MIF and Flag-VAMP4 were treated with cold digitonin (50 µg/ml), immunostained with an anti-Flag antibody, and imaged by fluorescence microscopy. (H, lower) HeLa cells expressing GFP-VAMP8 and mCherry-MIF were treated with cold digitonin (50 µg/ml) and imaged by fluorescence microscopy.
    Figure Legend Snippet: Effect of autophagy on MIF secretion. (A) HeLa cells expressing GFP-LC3 and mCherry-MIF were treated with cold digitonin (50 µg/ml) and imaged by fluorescence microscopy. (B) Secretion of MIF was measured in HEK293T cells either untreated or treated with 10 μM SAR405. (C) Secretion of MIF was measured in HEK293T cells treated with control siRNA or siRNA targeting ATG5 for 72 h. (D) Secretion of MIF was measured in HEK293T cells either untreated or treated with 100 nM bafilomycin A1. (E) Secretion of MIF was measured in HEK293T cells treated with control siRNA or siRNA targeting SYT5 for 48 h. Knockdown efficiency was confirmed by immunoblotting for SYT5. (F) Secretion of Flag-MIF was measured in HEK293T cells expressing mock or GFP-SEC22B. (G) HeLa cells expressing GFP-SEC22B and mCherry-MIF were treated with cold digitonin (50 µg/ml) and imaged by fluorescence microscopy. (H, upper) HeLa cells co-expressing GFP-MIF and Flag-VAMP4 were treated with cold digitonin (50 µg/ml), immunostained with an anti-Flag antibody, and imaged by fluorescence microscopy. (H, lower) HeLa cells expressing GFP-VAMP8 and mCherry-MIF were treated with cold digitonin (50 µg/ml) and imaged by fluorescence microscopy.

    Techniques Used: Expressing, Fluorescence, Microscopy, Control, Knockdown, Western Blot

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    Article Snippet: .. siRNAs (SC-43139) and negative control siRNA (SC-37007), used to target lymphocyte JAM-A genes, were purchased from Santa Cruz Biotechnology, USA. .. To overexpress exogenous human JAM-A protein in human lymphocytes, a retroviral expression vector carrying the entire coding sequence of JAM-A (NCBI, GenBank: BC001533.2) was amplified with PCR and sub-cloned into retroviral expression vector pBabe-puro (pBabe-JAM-A, Addgene) using primer sets including BamHI and SalI unique restriction sites (Table 2).

    Article Title: Notoginsenoside R1 mitigates UVB-induced skin sunburn injury through modulation of N 4 -acetylcytidine and autophagy
    Article Snippet: .. The following siRNAs were used: siRNA-ATG7 (sc-41447), siRNA-ATG5 (sc-41445), siRNA-NAT10 (sc-62660), and negative control siRNA (sc-37007), all purchased from Santa Cruz Biotechnology. ..

    Article Title: Pharmacological inhibition of the interleukin-1 receptor-associated kinase prevents angiotensin II-induced cardiac remodelling in mice.
    Article Snippet: Correspondence Manoj Kumar Barthwal, Pharmacology Division, Council of Scientific and Industrial Research-Central Drug Research Institute (CSIR-CDRI), Lucknow, 226031, India.. Email: manojbarthwal@cdri.res.in Background and Purpose: Angiotensin II (AngII) induces cardiac hypertrophy but the exact mechanism is not known.. The present study investigates the role of the interleukin-1 receptor-associated kinase (IRAK), in AngII-induced cardiac inflammation, fibrosis and hypertrophy.

    Article Title: Notoginsenoside R1 mitigates UVB-induced skin sunburn injury through modulation of N 4 -acetylcytidine and autophagy.
    Article Snippet: .. After incubation, total protein was extracted and subjected to immunoblotting to assess the expression levels of NAT10 and the loading control GAPDH, to determine the potential degradation pathway involved in NAT10 regulation. siRNA transfection The following siRNAs were used: siRNA-ATG7 (sc41447), siRNA-ATG5 (sc-41445), siRNA-NAT10 (sc62660), and negative control siRNA (sc-37007), all purchased from Santa Cruz Biotechnology. .. Following 24 h of UVB irradiation, HaCaT cells were treated with either the proteasome inhibitor MG132 (10 μM) or the lysosomal inhibitor bafilomycin A1 (BafA1, 50 ng/mL) for 6 or 24 h, while a control group remained untreated.

    Article Title: Neohesperidin from <i>Aurantii Fructus Immaturus</i> Exerts Antidepressant-Like Effects and Modulates Glucocorticoid Receptor Signaling in a Chronic Stress Model
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    Article Title: Cholesterol in glioblastoma: impaired Hh signaling enhances epigenetic modifiers and decreases CAV1.
    Article Snippet: Caveolin siRNA (Sigma.) (5’- CAUCUACAAGCCCAACAACTT-3’ (sense), 5’-GUUGUUGGGCUUGUAGAUGTT-3’ (antisense) was transfected for 48 hrs (Deb et al., 2016). .. A negative control siRNA (sc-37007; Santa Cruz) was used to determine the baseline changes induced by siRNA transfections. ..

    Article Title: Aberrant Hippo-YAP/TEAD Signaling Drives Malignant Transcriptional Reprogramming in External Auditory Canal Squamous Cell Carcinoma
    Article Snippet: .. Pooled siRNAs (20 nmol/L) for PITX2 (#sc44016, Santa Cruz Biotechnology) and negative control siRNA (#sc37007, Santa Cruz Biotechnology) were transfected into cells using Lipofectamine RNAiMAX (#13778150, Thermo Fisher Scientific) according to the manufacturer’s protocol. ..

    Incubation:

    Article Title: Notoginsenoside R1 mitigates UVB-induced skin sunburn injury through modulation of N 4 -acetylcytidine and autophagy.
    Article Snippet: .. After incubation, total protein was extracted and subjected to immunoblotting to assess the expression levels of NAT10 and the loading control GAPDH, to determine the potential degradation pathway involved in NAT10 regulation. siRNA transfection The following siRNAs were used: siRNA-ATG7 (sc41447), siRNA-ATG5 (sc-41445), siRNA-NAT10 (sc62660), and negative control siRNA (sc-37007), all purchased from Santa Cruz Biotechnology. .. Following 24 h of UVB irradiation, HaCaT cells were treated with either the proteasome inhibitor MG132 (10 μM) or the lysosomal inhibitor bafilomycin A1 (BafA1, 50 ng/mL) for 6 or 24 h, while a control group remained untreated.

    Western Blot:

    Article Title: Notoginsenoside R1 mitigates UVB-induced skin sunburn injury through modulation of N 4 -acetylcytidine and autophagy.
    Article Snippet: .. After incubation, total protein was extracted and subjected to immunoblotting to assess the expression levels of NAT10 and the loading control GAPDH, to determine the potential degradation pathway involved in NAT10 regulation. siRNA transfection The following siRNAs were used: siRNA-ATG7 (sc41447), siRNA-ATG5 (sc-41445), siRNA-NAT10 (sc62660), and negative control siRNA (sc-37007), all purchased from Santa Cruz Biotechnology. .. Following 24 h of UVB irradiation, HaCaT cells were treated with either the proteasome inhibitor MG132 (10 μM) or the lysosomal inhibitor bafilomycin A1 (BafA1, 50 ng/mL) for 6 or 24 h, while a control group remained untreated.

    Expressing:

    Article Title: Notoginsenoside R1 mitigates UVB-induced skin sunburn injury through modulation of N 4 -acetylcytidine and autophagy.
    Article Snippet: .. After incubation, total protein was extracted and subjected to immunoblotting to assess the expression levels of NAT10 and the loading control GAPDH, to determine the potential degradation pathway involved in NAT10 regulation. siRNA transfection The following siRNAs were used: siRNA-ATG7 (sc41447), siRNA-ATG5 (sc-41445), siRNA-NAT10 (sc62660), and negative control siRNA (sc-37007), all purchased from Santa Cruz Biotechnology. .. Following 24 h of UVB irradiation, HaCaT cells were treated with either the proteasome inhibitor MG132 (10 μM) or the lysosomal inhibitor bafilomycin A1 (BafA1, 50 ng/mL) for 6 or 24 h, while a control group remained untreated.

    Control:

    Article Title: Notoginsenoside R1 mitigates UVB-induced skin sunburn injury through modulation of N 4 -acetylcytidine and autophagy.
    Article Snippet: .. After incubation, total protein was extracted and subjected to immunoblotting to assess the expression levels of NAT10 and the loading control GAPDH, to determine the potential degradation pathway involved in NAT10 regulation. siRNA transfection The following siRNAs were used: siRNA-ATG7 (sc41447), siRNA-ATG5 (sc-41445), siRNA-NAT10 (sc62660), and negative control siRNA (sc-37007), all purchased from Santa Cruz Biotechnology. .. Following 24 h of UVB irradiation, HaCaT cells were treated with either the proteasome inhibitor MG132 (10 μM) or the lysosomal inhibitor bafilomycin A1 (BafA1, 50 ng/mL) for 6 or 24 h, while a control group remained untreated.

    Transfection:

    Article Title: Notoginsenoside R1 mitigates UVB-induced skin sunburn injury through modulation of N 4 -acetylcytidine and autophagy.
    Article Snippet: .. After incubation, total protein was extracted and subjected to immunoblotting to assess the expression levels of NAT10 and the loading control GAPDH, to determine the potential degradation pathway involved in NAT10 regulation. siRNA transfection The following siRNAs were used: siRNA-ATG7 (sc41447), siRNA-ATG5 (sc-41445), siRNA-NAT10 (sc62660), and negative control siRNA (sc-37007), all purchased from Santa Cruz Biotechnology. .. Following 24 h of UVB irradiation, HaCaT cells were treated with either the proteasome inhibitor MG132 (10 μM) or the lysosomal inhibitor bafilomycin A1 (BafA1, 50 ng/mL) for 6 or 24 h, while a control group remained untreated.

    Article Title: Cholesterol in glioblastoma: impaired Hh signaling enhances epigenetic modifiers and decreases CAV1.
    Article Snippet: Caveolin siRNA (Sigma.) (5’- CAUCUACAAGCCCAACAACTT-3’ (sense), 5’-GUUGUUGGGCUUGUAGAUGTT-3’ (antisense) was transfected for 48 hrs (Deb et al., 2016). .. A negative control siRNA (sc-37007; Santa Cruz) was used to determine the baseline changes induced by siRNA transfections. ..

    Article Title: Aberrant Hippo-YAP/TEAD Signaling Drives Malignant Transcriptional Reprogramming in External Auditory Canal Squamous Cell Carcinoma
    Article Snippet: .. Pooled siRNAs (20 nmol/L) for PITX2 (#sc44016, Santa Cruz Biotechnology) and negative control siRNA (#sc37007, Santa Cruz Biotechnology) were transfected into cells using Lipofectamine RNAiMAX (#13778150, Thermo Fisher Scientific) according to the manufacturer’s protocol. ..



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    Relationship between MIF and TMED10. (A) Secretion of MIF was measured in HEK293T cells either untreated or treated with brefeldin A. (B) Secretion of MIF was measured in HEK293T cells untreated or treated with the indicated doses of probenecid. (C) GST or the indicated GST-TMED10 domains coupled to glutathione sepharose beads were incubated with whole cell lysates from HEK293T cells expressing Flag-MIF. Elutes were subjected to SDS-PAGE and immunoblotted with an anti-Flag antibody. (D) GST-MIF coupled to glutathione sepharose beads was incubated with whole cell lysate from HEK293T cells expressing GFP-TMED10 or GFP-TMED10(ΔCT). Elutes were subjected to SDS-PAGE and immunoblotted with anti-GFP antibody. (E) Secretion of MIF was measured in HEK293T cells expressing mock or GFP-TMED10. (F) Secretion of MIF was measured in HEK293T cells treated with control <t>siRNA</t> or siRNA targeting TMED10 for 72 h. (G) A crosslink assay was performed in HEK293T cells expressing GFP-TMED10 with mock or Flag-MIF to examine the oligomeric form of TMED10. (H) Secretion of Flag-MIF was measured in HEK293T cells expressing mock, RAB1A, 1B, and 2A.
    Shrna Negative Control, supplied by Genechem, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Relationship between MIF and TMED10. (A) Secretion of MIF was measured in HEK293T cells either untreated or treated with brefeldin A. (B) Secretion of MIF was measured in HEK293T cells untreated or treated with the indicated doses of probenecid. (C) GST or the indicated GST-TMED10 domains coupled to glutathione sepharose beads were incubated with whole cell lysates from HEK293T cells expressing Flag-MIF. Elutes were subjected to SDS-PAGE and immunoblotted with an anti-Flag antibody. (D) GST-MIF coupled to glutathione sepharose beads was incubated with whole cell lysate from HEK293T cells expressing GFP-TMED10 or GFP-TMED10(ΔCT). Elutes were subjected to SDS-PAGE and immunoblotted with anti-GFP antibody. (E) Secretion of MIF was measured in HEK293T cells expressing mock or GFP-TMED10. (F) Secretion of MIF was measured in HEK293T cells treated with control siRNA or siRNA targeting TMED10 for 72 h. (G) A crosslink assay was performed in HEK293T cells expressing GFP-TMED10 with mock or Flag-MIF to examine the oligomeric form of TMED10. (H) Secretion of Flag-MIF was measured in HEK293T cells expressing mock, RAB1A, 1B, and 2A.

    Journal: Autophagy Reports

    Article Title: TRPML3 and TRPML1/3 differentially regulate unconventional MIF secretion through TMED10 and secretory autophagy

    doi: 10.1080/27694127.2026.2740425

    Figure Lengend Snippet: Relationship between MIF and TMED10. (A) Secretion of MIF was measured in HEK293T cells either untreated or treated with brefeldin A. (B) Secretion of MIF was measured in HEK293T cells untreated or treated with the indicated doses of probenecid. (C) GST or the indicated GST-TMED10 domains coupled to glutathione sepharose beads were incubated with whole cell lysates from HEK293T cells expressing Flag-MIF. Elutes were subjected to SDS-PAGE and immunoblotted with an anti-Flag antibody. (D) GST-MIF coupled to glutathione sepharose beads was incubated with whole cell lysate from HEK293T cells expressing GFP-TMED10 or GFP-TMED10(ΔCT). Elutes were subjected to SDS-PAGE and immunoblotted with anti-GFP antibody. (E) Secretion of MIF was measured in HEK293T cells expressing mock or GFP-TMED10. (F) Secretion of MIF was measured in HEK293T cells treated with control siRNA or siRNA targeting TMED10 for 72 h. (G) A crosslink assay was performed in HEK293T cells expressing GFP-TMED10 with mock or Flag-MIF to examine the oligomeric form of TMED10. (H) Secretion of Flag-MIF was measured in HEK293T cells expressing mock, RAB1A, 1B, and 2A.

    Article Snippet: For knockdown experiments, siRNA targeting human TMED10 (BIONEER, 10,972–1), human ATG5 (BIONEER, 9474–1), human SYT5 (BIONEER, 6861–1), and a negative control scrambled siRNA (Santa Cruz Biotechnology, sc-37007) were used.

    Techniques: Incubation, Expressing, SDS Page, Control

    Effect of autophagy on MIF secretion. (A) HeLa cells expressing GFP-LC3 and mCherry-MIF were treated with cold digitonin (50 µg/ml) and imaged by fluorescence microscopy. (B) Secretion of MIF was measured in HEK293T cells either untreated or treated with 10 μM SAR405. (C) Secretion of MIF was measured in HEK293T cells treated with control siRNA or siRNA targeting ATG5 for 72 h. (D) Secretion of MIF was measured in HEK293T cells either untreated or treated with 100 nM bafilomycin A1. (E) Secretion of MIF was measured in HEK293T cells treated with control siRNA or siRNA targeting SYT5 for 48 h. Knockdown efficiency was confirmed by immunoblotting for SYT5. (F) Secretion of Flag-MIF was measured in HEK293T cells expressing mock or GFP-SEC22B. (G) HeLa cells expressing GFP-SEC22B and mCherry-MIF were treated with cold digitonin (50 µg/ml) and imaged by fluorescence microscopy. (H, upper) HeLa cells co-expressing GFP-MIF and Flag-VAMP4 were treated with cold digitonin (50 µg/ml), immunostained with an anti-Flag antibody, and imaged by fluorescence microscopy. (H, lower) HeLa cells expressing GFP-VAMP8 and mCherry-MIF were treated with cold digitonin (50 µg/ml) and imaged by fluorescence microscopy.

    Journal: Autophagy Reports

    Article Title: TRPML3 and TRPML1/3 differentially regulate unconventional MIF secretion through TMED10 and secretory autophagy

    doi: 10.1080/27694127.2026.2740425

    Figure Lengend Snippet: Effect of autophagy on MIF secretion. (A) HeLa cells expressing GFP-LC3 and mCherry-MIF were treated with cold digitonin (50 µg/ml) and imaged by fluorescence microscopy. (B) Secretion of MIF was measured in HEK293T cells either untreated or treated with 10 μM SAR405. (C) Secretion of MIF was measured in HEK293T cells treated with control siRNA or siRNA targeting ATG5 for 72 h. (D) Secretion of MIF was measured in HEK293T cells either untreated or treated with 100 nM bafilomycin A1. (E) Secretion of MIF was measured in HEK293T cells treated with control siRNA or siRNA targeting SYT5 for 48 h. Knockdown efficiency was confirmed by immunoblotting for SYT5. (F) Secretion of Flag-MIF was measured in HEK293T cells expressing mock or GFP-SEC22B. (G) HeLa cells expressing GFP-SEC22B and mCherry-MIF were treated with cold digitonin (50 µg/ml) and imaged by fluorescence microscopy. (H, upper) HeLa cells co-expressing GFP-MIF and Flag-VAMP4 were treated with cold digitonin (50 µg/ml), immunostained with an anti-Flag antibody, and imaged by fluorescence microscopy. (H, lower) HeLa cells expressing GFP-VAMP8 and mCherry-MIF were treated with cold digitonin (50 µg/ml) and imaged by fluorescence microscopy.

    Article Snippet: For knockdown experiments, siRNA targeting human TMED10 (BIONEER, 10,972–1), human ATG5 (BIONEER, 9474–1), human SYT5 (BIONEER, 6861–1), and a negative control scrambled siRNA (Santa Cruz Biotechnology, sc-37007) were used.

    Techniques: Expressing, Fluorescence, Microscopy, Control, Knockdown, Western Blot