mouse heart tissue lysate Search Results


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Mouse Heart Tissue Lysate Lyophilized from Innovative Research is provided as a Lyophilized powder. This product is lyophilized with SDS-PAGE buffer containing the reducing agent DTT. Reconstitute using sterile distilled water or PBS, adding glycerol
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90
Novus Biologicals mouse heart tissue lysate
FIG. 2. Immunoblot analysis of TLR proteins in male reproductive organs. Aliquots (100 lg) of cytoplasmic protein extracts were separated by PAGE, electroblotted, and blots probed with anti-TLR antibodies followed by enhanced chemiluminescence detection using Pierce Super- Signal West Pico or Pierce SuperSignal West Femto (*F) substrate. Representative results are shown (n ¼ 3–5 rats). þ, control rat <t>tissue</t> extracts from spleen, TLRs 1–7; lung, TLR8; and small intestine, TLR9. þ Ext, positive-control whole cell lysates used were Raw 264 Abelson transformed macrophages (TLRs 1, 2–6, and 8–10); SW480 colorectal adenocarcinoma (TLR2); Daudi cell extract (TLR7); Ramos cell <t>lysate</t> (TLR10) and <t>mouse</t> <t>heart</t> whole cell lysate (TLR11). Blots were stripped and reprobed with anti-actin monoclonal antibody to detect actin as a loading control. Representative results are shown (n ¼ 3–5 rats) for blots exposed to film for the same length of time when using equivalent chemiluminescent substrate.
Mouse Heart Tissue Lysate, supplied by Novus Biologicals, 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/mouse+heart+tissue+lysate/pm17314314-60-0-12?v=Novus+Biologicals
Average 90 stars, based on 1 article reviews
mouse heart tissue lysate - by Bioz Stars, 2026-08
90/100 stars
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92
Novus Biologicals mouse heart lysate
FIG. 2. Immunoblot analysis of TLR proteins in male reproductive organs. Aliquots (100 lg) of cytoplasmic protein extracts were separated by PAGE, electroblotted, and blots probed with anti-TLR antibodies followed by enhanced chemiluminescence detection using Pierce Super- Signal West Pico or Pierce SuperSignal West Femto (*F) substrate. Representative results are shown (n ¼ 3–5 rats). þ, control rat <t>tissue</t> extracts from spleen, TLRs 1–7; lung, TLR8; and small intestine, TLR9. þ Ext, positive-control whole cell lysates used were Raw 264 Abelson transformed macrophages (TLRs 1, 2–6, and 8–10); SW480 colorectal adenocarcinoma (TLR2); Daudi cell extract (TLR7); Ramos cell <t>lysate</t> (TLR10) and <t>mouse</t> <t>heart</t> whole cell lysate (TLR11). Blots were stripped and reprobed with anti-actin monoclonal antibody to detect actin as a loading control. Representative results are shown (n ¼ 3–5 rats) for blots exposed to film for the same length of time when using equivalent chemiluminescent substrate.
Mouse Heart Lysate, supplied by Novus Biologicals, 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/mouse+heart+tissue+lysate/pm35860280-60-33-36?v=Novus+Biologicals
Average 92 stars, based on 1 article reviews
mouse heart lysate - by Bioz Stars, 2026-08
92/100 stars
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Mouse Age 7 Days Heart Tissue Lysate from Innovative Research is provided as a Liquid buffered in SDS sample buffer containing 5% beta-mercaptoethanol with a concentration of 2mg/ml. This product is especially useful for applications
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Mouse Heart Tissue Lysate from Innovative Research is provided with a concentration of 2mg/ml. This product is especially useful for applications like Western Blot, among others. For continuous use, store at 2-8°C. If not using
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Mouse tPA Genetically Deficient Heart Tissue Lysate from Innovative Research is prepared from a tPA knockout mouse. This Tissue Plasminogen Activator (tPA) Knockout was created by targeted disruption of the PLAT gene. Mutations were then
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Mouse Age 0 Days Heart Tissue Lysate from Innovative Research is provided as a Liquid buffered in SDS sample buffer containing 5% beta-mercaptoethanol with a concentration of 2mg/ml. This product is especially useful for applications
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Mouse Factor XII Genetically Deficient Heart Tissue Lysate from Innovative Research is prepared from a Factor XII knockout mouse. This Factor XII Knockout was created by targeted disruption of the F12 gene. Mutations were then
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Mouse Age 14 Days Heart Tissue Lysate from Innovative Research is provided as a Liquid buffered in SDS sample buffer containing 5% beta-mercaptoethanol with a concentration of 2mg/ml. This product is especially useful for applications
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Mouse C1 Inhibitor Genetically Deficient Heart Tissue Lysate from Innovative Research is prepared from a C1 Inhibitor Homozygous Knockout Mouse. This C1 Inhibitor Homozygous Knockout was created by targeted excision of the SERPING1 gene. Homozygous
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FIG. 2. Immunoblot analysis of TLR proteins in male reproductive organs. Aliquots (100 lg) of cytoplasmic protein extracts were separated by PAGE, electroblotted, and blots probed with anti-TLR antibodies followed by enhanced chemiluminescence detection using Pierce Super- Signal West Pico or Pierce SuperSignal West Femto (*F) substrate. Representative results are shown (n ¼ 3–5 rats). þ, control rat tissue extracts from spleen, TLRs 1–7; lung, TLR8; and small intestine, TLR9. þ Ext, positive-control whole cell lysates used were Raw 264 Abelson transformed macrophages (TLRs 1, 2–6, and 8–10); SW480 colorectal adenocarcinoma (TLR2); Daudi cell extract (TLR7); Ramos cell lysate (TLR10) and mouse heart whole cell lysate (TLR11). Blots were stripped and reprobed with anti-actin monoclonal antibody to detect actin as a loading control. Representative results are shown (n ¼ 3–5 rats) for blots exposed to film for the same length of time when using equivalent chemiluminescent substrate.

Journal: Biology of reproduction

Article Title: Members of the Toll-like receptor family of innate immunity pattern-recognition receptors are abundant in the male rat reproductive tract.

doi: 10.1095/biolreprod.106.059410

Figure Lengend Snippet: FIG. 2. Immunoblot analysis of TLR proteins in male reproductive organs. Aliquots (100 lg) of cytoplasmic protein extracts were separated by PAGE, electroblotted, and blots probed with anti-TLR antibodies followed by enhanced chemiluminescence detection using Pierce Super- Signal West Pico or Pierce SuperSignal West Femto (*F) substrate. Representative results are shown (n ¼ 3–5 rats). þ, control rat tissue extracts from spleen, TLRs 1–7; lung, TLR8; and small intestine, TLR9. þ Ext, positive-control whole cell lysates used were Raw 264 Abelson transformed macrophages (TLRs 1, 2–6, and 8–10); SW480 colorectal adenocarcinoma (TLR2); Daudi cell extract (TLR7); Ramos cell lysate (TLR10) and mouse heart whole cell lysate (TLR11). Blots were stripped and reprobed with anti-actin monoclonal antibody to detect actin as a loading control. Representative results are shown (n ¼ 3–5 rats) for blots exposed to film for the same length of time when using equivalent chemiluminescent substrate.

Article Snippet: Mouse heart tissue lysate (40102) and Ramos cell lysate (40175) was from Imgenex.

Techniques: Western Blot, Control, Positive Control, Transformation Assay