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phsl  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc phsl
    Phsl, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 488 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+phsl/Phospho-HSL+(Ser563)+Antibody/bio_rxiv__64898__2026__03__20__712802-288-31-32
    Average 96 stars, based on 488 article reviews
    phsl - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Membrane:

    Article Title: Sodium-potassium Adenosine Triphosphatase α2 Subunit (ATP1A2) Negatively Regulates UCP1-dependent and UCP1-independent Thermogenesis in 3T3-L1 Adipocytes
    Article Snippet: Increasing the number of brite cells (browning) in white adipocytes has attracted considerable attention to combat obesity because brite cells also help elevate energy expenditure.. Sodium-potassium adenosine triphosphatase α2 subunit (ATP1A2) has been studied extensively in migraine and cancers.. On the other hand, the role of ATP1A2 in adipocytes biology with a focus on fat browning needs to be elucidated.

    Article Title: Loss of family with sequence similarity 107, member A (FAM107A) induces browning in 3T3-L1 adipocytes.
    Article Snippet: Induction of white fat browning (beiging) and activation of brown fat has been considered a promising strategy to treat obesity and associated metabolic complications.. However, the molecular mechanisms regulating brown and beige fat-mediated thermogenesis remains unclear.. Our study aimed to identify genes with a hitherto unknown mechanism in the metabolic functions of adipocytes and identified family with sequence similarity 107, member A (FAM107A) as a factor that interferes with fat browning in white adipocytes.

    Article Title: ATP1A2 negatively regulates myogenic differentiation and thermogenesis in C2C12 myoblasts
    Article Snippet: It is well documented that the α2 subunit of Na+/K+-ATPase (ATP1A2) positively regulates obesity, cardiovascular disease, and diabetes, and additionally indirectly controls cellular Ca2+ homeostasis.. However, the functional role of ATP1A2 in the muscle remains unexplored.. Here, we investigated the functional role of ATP1A2 in muscle physiology with a focus on thermogenesis, using mouse-derived C2C12 myoblasts.

    Incubation:

    Article Title: Sodium-potassium Adenosine Triphosphatase α2 Subunit (ATP1A2) Negatively Regulates UCP1-dependent and UCP1-independent Thermogenesis in 3T3-L1 Adipocytes
    Article Snippet: Increasing the number of brite cells (browning) in white adipocytes has attracted considerable attention to combat obesity because brite cells also help elevate energy expenditure.. Sodium-potassium adenosine triphosphatase α2 subunit (ATP1A2) has been studied extensively in migraine and cancers.. On the other hand, the role of ATP1A2 in adipocytes biology with a focus on fat browning needs to be elucidated.

    Article Title: The development of metabolic endotoxemia is dependent on the type of sweetener and the presence of saturated fat in the diet.
    Article Snippet: .. Membranes were blocked in a blocking buffer consisting of 3% BSA in TBS Tween for 60 min at room temperature and incubated overnight at 4oC with the primary antibody and the following primary and secondary antibodies in the blocking buffer: anti-pHSL (Cell Signaling, 4139, rabbit polyclonal IgG) at 1:1000; anti-TLR4 (Santa Cruz, SC-293072, mouse monoclonal IgG) at 1:1000; anti-TLR2 (Santa Cruz, SC-10739, rabbit polyclonal IgG) at 1:1000; anti-NFKB (Santa Cruz, SC-372, rabbit polyclonal) at 1:1500; anti-occludin (Abcam, AB167161, rabbit monoclonal IgG) at 1:100,000; anti-GPR41 (LSBio, LS-C357088-100, rabbit polyclonal) at 1:1500; and anti-GPR43 (Santa Cruz, SC-32906, rabbit polyclonal) at 1:1500. .. The blots were incubated with anti-rabbit (Abcam, AB6885) or anti-mouse (Abcam, AB6789) secondary antibodies conjugated with horseradish peroxidase (1:15000).

    Article Title: The development of metabolic endotoxemia is dependent on the type of sweetener and the presence of saturated fat in the diet
    Article Snippet: .. Membranes were blocked in a blocking buffer consisting of 3% BSA in TBS Tween for 60 min at room temperature and incubated overnight at 4oC with the primary antibody and the following primary and secondary antibodies in the blocking buffer: anti-pHSL (Cell Signaling, 4139, rabbit polyclonal IgG) at 1:1000; anti-TLR4 (Santa Cruz, SC-293072, mouse monoclonal IgG) at 1:1000; anti-TLR2 (Santa Cruz, SC-10739, rabbit polyclonal IgG) at 1:1000; anti-NFKB (Santa Cruz, SC-372, rabbit polyclonal) at 1:1500; anti-occludin (Abcam, AB167161, rabbit monoclonal IgG) at 1:100,000; anti-GPR41 (LSBio, LS-C357088-100, rabbit polyclonal) at 1:1500; and anti-GPR43 (Santa Cruz, SC-32906, rabbit polyclonal) at 1:1500. .. The blots were incubated with anti-rabbit (Abcam, AB6885) or anti-mouse (Abcam, AB6789) secondary antibodies conjugated with horseradish peroxidase (1:15000).

    Article Title: Loss of family with sequence similarity 107, member A (FAM107A) induces browning in 3T3-L1 adipocytes.
    Article Snippet: Induction of white fat browning (beiging) and activation of brown fat has been considered a promising strategy to treat obesity and associated metabolic complications.. However, the molecular mechanisms regulating brown and beige fat-mediated thermogenesis remains unclear.. Our study aimed to identify genes with a hitherto unknown mechanism in the metabolic functions of adipocytes and identified family with sequence similarity 107, member A (FAM107A) as a factor that interferes with fat browning in white adipocytes.

    Article Title: A bioenergetic basis for multiorgan dysfunction in sepsis
    Article Snippet: .. Samples were incubated with anti-ATGL (PNPLA2/ATGL Antibody, Novus biologicals, Cat#: AF5365, 1:800) and anti-pHSL (Phospho-HSL Ser660, Cat#16745804S, Cell Signaling Technology, 1:600) primary antibodies, in blocking buffer (3 days, RT; shaking) followed by washing (PtxwH buffer, 5x 1 hour each). .. Samples were incubated with secondary antibody, Donkey anti-Sheep IgG H&L (Alexa Fluor® 647, 1:400; Abcam, Cat#ab150179) and Donkey Anti-Rabbit IgG H&L (Alexa Fluor® 568, 1:400; Abcam, Cat#ab175470) in blocking buffer (overnight, RT, shaking) followed by washing (PtxwH buffer 5x, 30 min. each).

    Article Title: ATP1A2 negatively regulates myogenic differentiation and thermogenesis in C2C12 myoblasts
    Article Snippet: It is well documented that the α2 subunit of Na+/K+-ATPase (ATP1A2) positively regulates obesity, cardiovascular disease, and diabetes, and additionally indirectly controls cellular Ca2+ homeostasis.. However, the functional role of ATP1A2 in the muscle remains unexplored.. Here, we investigated the functional role of ATP1A2 in muscle physiology with a focus on thermogenesis, using mouse-derived C2C12 myoblasts.

    Blocking Assay:

    Article Title: The development of metabolic endotoxemia is dependent on the type of sweetener and the presence of saturated fat in the diet.
    Article Snippet: .. Membranes were blocked in a blocking buffer consisting of 3% BSA in TBS Tween for 60 min at room temperature and incubated overnight at 4oC with the primary antibody and the following primary and secondary antibodies in the blocking buffer: anti-pHSL (Cell Signaling, 4139, rabbit polyclonal IgG) at 1:1000; anti-TLR4 (Santa Cruz, SC-293072, mouse monoclonal IgG) at 1:1000; anti-TLR2 (Santa Cruz, SC-10739, rabbit polyclonal IgG) at 1:1000; anti-NFKB (Santa Cruz, SC-372, rabbit polyclonal) at 1:1500; anti-occludin (Abcam, AB167161, rabbit monoclonal IgG) at 1:100,000; anti-GPR41 (LSBio, LS-C357088-100, rabbit polyclonal) at 1:1500; and anti-GPR43 (Santa Cruz, SC-32906, rabbit polyclonal) at 1:1500. .. The blots were incubated with anti-rabbit (Abcam, AB6885) or anti-mouse (Abcam, AB6789) secondary antibodies conjugated with horseradish peroxidase (1:15000).

    Article Title: The development of metabolic endotoxemia is dependent on the type of sweetener and the presence of saturated fat in the diet
    Article Snippet: .. Membranes were blocked in a blocking buffer consisting of 3% BSA in TBS Tween for 60 min at room temperature and incubated overnight at 4oC with the primary antibody and the following primary and secondary antibodies in the blocking buffer: anti-pHSL (Cell Signaling, 4139, rabbit polyclonal IgG) at 1:1000; anti-TLR4 (Santa Cruz, SC-293072, mouse monoclonal IgG) at 1:1000; anti-TLR2 (Santa Cruz, SC-10739, rabbit polyclonal IgG) at 1:1000; anti-NFKB (Santa Cruz, SC-372, rabbit polyclonal) at 1:1500; anti-occludin (Abcam, AB167161, rabbit monoclonal IgG) at 1:100,000; anti-GPR41 (LSBio, LS-C357088-100, rabbit polyclonal) at 1:1500; and anti-GPR43 (Santa Cruz, SC-32906, rabbit polyclonal) at 1:1500. .. The blots were incubated with anti-rabbit (Abcam, AB6885) or anti-mouse (Abcam, AB6789) secondary antibodies conjugated with horseradish peroxidase (1:15000).

    Article Title: A bioenergetic basis for multiorgan dysfunction in sepsis
    Article Snippet: .. Samples were incubated with anti-ATGL (PNPLA2/ATGL Antibody, Novus biologicals, Cat#: AF5365, 1:800) and anti-pHSL (Phospho-HSL Ser660, Cat#16745804S, Cell Signaling Technology, 1:600) primary antibodies, in blocking buffer (3 days, RT; shaking) followed by washing (PtxwH buffer, 5x 1 hour each). .. Samples were incubated with secondary antibody, Donkey anti-Sheep IgG H&L (Alexa Fluor® 647, 1:400; Abcam, Cat#ab150179) and Donkey Anti-Rabbit IgG H&L (Alexa Fluor® 568, 1:400; Abcam, Cat#ab175470) in blocking buffer (overnight, RT, shaking) followed by washing (PtxwH buffer 5x, 30 min. each).

    Cell-Signaling:

    Article Title: Semaphorin 7A regulates axon outgrowth in subcutaneous white adipose tissue
    Article Snippet: .. Primary antibodies: anti-Cyclophilin B (21 kDa, 1:40,000, Abcam, Cat#16045), anti-beta-tubulin (55 kDa, 1:1000, Cell Signaling, Cat#2146), anti-ATGL (55 kDa, 1:1000, Cell Signaling, Cat#2138), anti-HSL (81 kDa, 1:1000, Cell Signaling, Cat#4107), anti-pHSL (81 kDa, 1:1000, Cell Signaling, Cat#2138), anti-UCP1 (32 kDa, 1:1000, Abcam, Cat#ab10983), anti-PGP9.5 (25 kDa, 1:750, Abcam, Cat#ab108986), anti-TH (62 kDa, 1:1000, Millipore EMD, Cat#ab152), anti-AVIL (92 kDa, 1:1000, Abcam, Cat#ab72210), anti-GAP43 (43 kDa, 1:10,000, Novus Biologicals, Cat#MB300-143), and anti-SYN1 (77 kDa, 1:1000, Cell Signaling, Cat#5297). .. Secondary antibodies: anti-rabbit HRP-linked secondary antibody (1:3000, Cell Signaling Technology, Cat#7074).

    Saline:

    Article Title: ATP1A2 negatively regulates myogenic differentiation and thermogenesis in C2C12 myoblasts
    Article Snippet: It is well documented that the α2 subunit of Na+/K+-ATPase (ATP1A2) positively regulates obesity, cardiovascular disease, and diabetes, and additionally indirectly controls cellular Ca2+ homeostasis.. However, the functional role of ATP1A2 in the muscle remains unexplored.. Here, we investigated the functional role of ATP1A2 in muscle physiology with a focus on thermogenesis, using mouse-derived C2C12 myoblasts.



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    Image Search Results


    PTHrP induces adipose browning through the PKA signaling pathway. (A-H) Adipocytes were subjected to two experimental treatments: (A, C, E, and G) adipocytes were treated with 100 ng/mL PTHrP or DMSO (vehicle control) in the presence or absence of H89 (50 µM), (B, D, F, and H) adipocytes with or without PTHR knockout were treated with bladder cancer cell-derived CM or control CM. (A and B) Representative immunoblots (left) of phosphorylated PKA substrates, p-HSL (Ser660), total HSL, p-CREB (Ser133), and total CREB in adipocytes with indicated treatments, with quantification (right) of the pHSL/total HSL and p-CREB/total CREB ratios. (C and D) Representative immunoblots (left) and quantification (right) of UCP1 in indicated adipocytes. (E and F) FFA release levels of indicated adipocytes were measured using a colorimetric assay. (G and H) Representative Oil Red O staining (left) and quantification (right) of neutral lipids in indicated adipocytes. Scale bars, 50 μm. Data were expressed as means ± SEM (A-H). * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 by one-way ANOVA (A-H).

    Journal: Neoplasia (New York, N.Y.)

    Article Title: White-to-brown adipose switching promotes bladder cancer progression

    doi: 10.1016/j.neo.2026.101282

    Figure Lengend Snippet: PTHrP induces adipose browning through the PKA signaling pathway. (A-H) Adipocytes were subjected to two experimental treatments: (A, C, E, and G) adipocytes were treated with 100 ng/mL PTHrP or DMSO (vehicle control) in the presence or absence of H89 (50 µM), (B, D, F, and H) adipocytes with or without PTHR knockout were treated with bladder cancer cell-derived CM or control CM. (A and B) Representative immunoblots (left) of phosphorylated PKA substrates, p-HSL (Ser660), total HSL, p-CREB (Ser133), and total CREB in adipocytes with indicated treatments, with quantification (right) of the pHSL/total HSL and p-CREB/total CREB ratios. (C and D) Representative immunoblots (left) and quantification (right) of UCP1 in indicated adipocytes. (E and F) FFA release levels of indicated adipocytes were measured using a colorimetric assay. (G and H) Representative Oil Red O staining (left) and quantification (right) of neutral lipids in indicated adipocytes. Scale bars, 50 μm. Data were expressed as means ± SEM (A-H). * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 by one-way ANOVA (A-H).

    Article Snippet: The membranes were then incubated with primary antibodies including anti-UCP1 (1:3000, 83870-1-RR, Proteintech, China), anti-PTHLH (1:2000, A3183, ABclonal, China), anti-PTHR (1:1000, 29115-1-AP, Proteintech, China), anti-Phospho-PKA Substrate (RRXS*/T*) (1:1000, 9624, CST, USA), anti-pHSL (Ser660) (1:1000, AF8026, Affinity, China), anti-HSL (1:1000, AF6403, Affinity, China), anti-pCREB (Ser133) (1:2000, 28792-1-AP, Proteintech, China), anti-CREB(1:5000, 12208-1-AP, Proteintech, China), anti-GAPDH (1:50000, HRP-60004, Proteintech, China) and anti-ɑTubulin (1:10000, HRP-80762, Proteintech, China) overnight at 4°C.

    Techniques: Control, Knock-Out, Derivative Assay, Western Blot, Colorimetric Assay, Staining