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rabbit anti leptin  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology rabbit anti leptin
    Rabbit Anti Leptin, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 351 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+leptin/Leptin/bio_rxiv__2025__07__23__666305-55-31-39
    Average 95 stars, based on 351 article reviews
    rabbit anti leptin - by Bioz Stars, 2026-10
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    Related Articles

    Incubation:

    Article Title: Human chorionic gonadotropin improves endometriosis through downregulation of leptin expression in rats.
    Article Snippet: Objective: To investigate whether and how human chorionic gonadotropin (HCG) treatment ameliorates endometriosis in an endometriotic rat model. Methods: Twentyfour endometriosis rats were established and were randomly divided into four groups, and then the rats were treated with 19.4, 25.8, and 51.6 IU/100 g weight/day of HCG, respectively.. The control group was treated with 0.9% NaCl.. After 15 days (3 estrous cycles), the ectopic lesion volume and the expression of leptin protein in eutopic and ectopic endometrium were investigated.

    Article Title: High-fat-diet-induced modulations of leptin signaling and gastric microbiota drive precancerous lesions in the stomach.
    Article Snippet: Accepted Manuscript High-fat diet-induced modulations of leptin signaling and gastric microbiota drive precancerous lesions in the stomach Seiya Arita , Kyoko Inagaki-Ohara PII: S0899-9007(19)30115-7 DOI: https://doi.org/10.1016/j.nut.2019.110556 Article Number: 110556 Reference: NUT 110556 To appear in: Nutrition Received date: 13 May 2019 Accepted date: 5 July 2019 Please cite this article as: Seiya Arita , Kyoko Inagaki-Ohara , High-fat diet-induced modulations of leptin signaling and gastric microbiota drive precancerous lesions in the stomach, Nutrition (2019), doi: https://doi.org/10.1016/j.nut.2019.110556 This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript.. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form.

    Article Title: Sex-specific hypothalamic axis disruption in the rNLS8 mouse model of amyotrophic lateral sclerosis (ALS)
    Article Snippet: RIPA buffer (Sigma Aldrich) containing a cocktail of protease inhibitors (Roche) as described previously [ ] was used to extract proteins from spinal cord. .. 20 μg of denatured protein samples from each group were electrophoresed into Bolt® Bis–Tris Plus gels (Invitrogen), transferred to PVDF membranes (BioRad) and incubated with primary antibodies [rabbit anti-ObRb (1:500; Abcam), rabbit anti-leptin (1:400, Invitro), mouse anti- STAT3 (1:500; Santa Cruz), rabbit anti-pSTAT3 (1:1000; Cell Signalling), mouse anti-Akt (1:500; Santa Cruz), rabbit anti-pAkt (1:500; Cell Signaling)] overnight. .. A corresponding anti-rabbit or anti-mouse horseradish peroxidase (HRP)-conjugated secondary antibody (Vector Laboratories) at dilution of 1:5000 was used as described previously [ ].

    Labeling:

    Article Title: Leptin Is Produced by Parathyroid Glands and Stimulates Parathyroid Hormone Secretion
    Article Snippet: Objective: We asked if leptin and its cognate receptor were present in normal and diseased parathyroid glands, and if so, whether they had any functional effects on parathyroid hormone (PTH) secretion in parathyroid neoplasms.. Background: The parathyroid glands acting through PTH play a critical role in the regulation of serum calcium.. Based on leptin’s recently discovered role in bone metabolism, we hypothesized these glands were the sites of a functional interaction between these 2 hormones.

    Blocking Assay:

    Article Title: Ectopic endometrium-derived leptin produces estrogen-dependent chronic pain in a rat model of endometriosis
    Article Snippet: .. The nitrocellulose membranes were saturated by shaking in blocking buffer [5% BSA in Tris-buffered saline containing 0.1% Tween20 (TBST)] for 1 h at room temperature (RT) and probed with rabbit anti-leptin (sc-842, 1:500, Santa Cruz Biotechnology, Santa Cruz, CA), or rabbit anti-β-actin (ab 8227, 1:500; Abcam, Cambridge, MA) antibodies in blocking buffer at 4°C overnight. .. After washing with TBST (3 times at RT, 15 min each) the leptin blot was probed with a biotinylated goat anti-rabbit antibody (1:1000 in blocking buffer, Jackson Immunoresearch, West Grove, PA) for 2 h at RT while the β-actin blot was probed with a horseradish peroxidase (HRP) conjugated anti-rabbit antibody (NA934V, 1:5000 in blocking buffer, GE Healthcare, Piscataway, NJ) for 2 h at RT.

    Saline:

    Article Title: Ectopic endometrium-derived leptin produces estrogen-dependent chronic pain in a rat model of endometriosis
    Article Snippet: .. The nitrocellulose membranes were saturated by shaking in blocking buffer [5% BSA in Tris-buffered saline containing 0.1% Tween20 (TBST)] for 1 h at room temperature (RT) and probed with rabbit anti-leptin (sc-842, 1:500, Santa Cruz Biotechnology, Santa Cruz, CA), or rabbit anti-β-actin (ab 8227, 1:500; Abcam, Cambridge, MA) antibodies in blocking buffer at 4°C overnight. .. After washing with TBST (3 times at RT, 15 min each) the leptin blot was probed with a biotinylated goat anti-rabbit antibody (1:1000 in blocking buffer, Jackson Immunoresearch, West Grove, PA) for 2 h at RT while the β-actin blot was probed with a horseradish peroxidase (HRP) conjugated anti-rabbit antibody (NA934V, 1:5000 in blocking buffer, GE Healthcare, Piscataway, NJ) for 2 h at RT.

    Western Blot:

    Article Title: Effects of acute intermittent hypoxia on energy balance and hypothalamic feeding pathways.
    Article Snippet: This study was done to investigate the effects of acute intermittent hypoxia (IH) onmetabolic factors associated with energy balance and body weight, and on hypothalamic satiety-inducing pathways.. Adult male Sprague–Dawley rats were exposed to either 8 h IH or normoxic control conditions.. Food intake, locomotion and body weights were examined after IH.



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    ABclonal Biotechnology anti rabbit leptin
    Experimental validation supports a senescence-associated role of LEP in EOPE. (A) qRT–PCR analysis of LEP, ENG, MIF and CYBB mRNA expression in PTB and EOPE placentas. n = 6 biologically independent placentas per group. Bars represent mean ± SD. (B) Representative images of senescence-associated β-galactosidase (SA-β-gal) staining. (C) Representative immunofluorescence images of P21 in PTB and EOPE placentas. Nuclei were counterstained with Hoechst. (D) Representative images of LEP immunohistochemistry in PTB and EOPE placentas. Scale bars, 100 μm. n = 6 biologically independent placentas per group. (E) Representative western blot showing LEP protein expression in PTB and EOPE placentas. n = 6. (F) Western blot analysis of P21 and LEP protein expression in BeWo cells treated with increasing concentrations of <t>leptin.</t> (G) Representative SA-β-gal staining images (left) and quantification of SA-β-gal-positive cells (right) in BeWo cells treated with leptin. n = 3 biologically independent experiments. Bars represent mean ± SD. (H) Detection of hCG in cell culture supernatant by ELISA after 24 h of leptin treatment.
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    Experimental validation supports a senescence-associated role of LEP in EOPE. (A) qRT–PCR analysis of LEP, ENG, MIF and CYBB mRNA expression in PTB and EOPE placentas. n = 6 biologically independent placentas per group. Bars represent mean ± SD. (B) Representative images of senescence-associated β-galactosidase (SA-β-gal) staining. (C) Representative immunofluorescence images of P21 in PTB and EOPE placentas. Nuclei were counterstained with Hoechst. (D) Representative images of LEP immunohistochemistry in PTB and EOPE placentas. Scale bars, 100 μm. n = 6 biologically independent placentas per group. (E) Representative western blot showing LEP protein expression in PTB and EOPE placentas. n = 6. (F) Western blot analysis of P21 and LEP protein expression in BeWo cells treated with increasing concentrations of <t>leptin.</t> (G) Representative SA-β-gal staining images (left) and quantification of SA-β-gal-positive cells (right) in BeWo cells treated with leptin. n = 3 biologically independent experiments. Bars represent mean ± SD. (H) Detection of hCG in cell culture supernatant by ELISA after 24 h of leptin treatment.
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    Experimental validation supports a senescence-associated role of LEP in EOPE. (A) qRT–PCR analysis of LEP, ENG, MIF and CYBB mRNA expression in PTB and EOPE placentas. n = 6 biologically independent placentas per group. Bars represent mean ± SD. (B) Representative images of senescence-associated β-galactosidase (SA-β-gal) staining. (C) Representative immunofluorescence images of P21 in PTB and EOPE placentas. Nuclei were counterstained with Hoechst. (D) Representative images of LEP immunohistochemistry in PTB and EOPE placentas. Scale bars, 100 μm. n = 6 biologically independent placentas per group. (E) Representative western blot showing LEP protein expression in PTB and EOPE placentas. n = 6. (F) Western blot analysis of P21 and LEP protein expression in BeWo cells treated with increasing concentrations of <t>leptin.</t> (G) Representative SA-β-gal staining images (left) and quantification of SA-β-gal-positive cells (right) in BeWo cells treated with leptin. n = 3 biologically independent experiments. Bars represent mean ± SD. (H) Detection of hCG in cell culture supernatant by ELISA after 24 h of leptin treatment.
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    The biomimetic periosteum increases PSCs accumulation in the bone defect region and upregulates periostin expression. (A) Immunofluorescence staining of PSCs (OSX + <t>LepR</t> + osteoprogenitors, yellow) in the bone defect region of the control, GC, GC-N, GC-NB and CM groups at 6 weeks. Scale bars, 500 μm. The higher-magnification images of the upper row (indicated by square boxes) are listed in the second row. Scale bars, 200 μm. (B) Immunofluorescence staining images of periostin in the femur defect at 6 weeks post-surgery. Scale bars, 100 μm. Data are presented as mean ± SD. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001. P, Periosteum; C, cortical bone; DAPI, 4′,6-diamidino-2-phenylindole; OSX, Osterix; LepR, <t>leptin</t> receptor; GC, biomimetic periosteum without Func-HA and BMP-2; GC-N, biomimetic periosteum without Func-HA; GC-NB, biomimetic periosteum; CM, collagen membrane. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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    The biomimetic periosteum increases PSCs accumulation in the bone defect region and upregulates periostin expression. (A) Immunofluorescence staining of PSCs (OSX + <t>LepR</t> + osteoprogenitors, yellow) in the bone defect region of the control, GC, GC-N, GC-NB and CM groups at 6 weeks. Scale bars, 500 μm. The higher-magnification images of the upper row (indicated by square boxes) are listed in the second row. Scale bars, 200 μm. (B) Immunofluorescence staining images of periostin in the femur defect at 6 weeks post-surgery. Scale bars, 100 μm. Data are presented as mean ± SD. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001. P, Periosteum; C, cortical bone; DAPI, 4′,6-diamidino-2-phenylindole; OSX, Osterix; LepR, <t>leptin</t> receptor; GC, biomimetic periosteum without Func-HA and BMP-2; GC-N, biomimetic periosteum without Func-HA; GC-NB, biomimetic periosteum; CM, collagen membrane. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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    The biomimetic periosteum increases PSCs accumulation in the bone defect region and upregulates periostin expression. (A) Immunofluorescence staining of PSCs (OSX + <t>LepR</t> + osteoprogenitors, yellow) in the bone defect region of the control, GC, GC-N, GC-NB and CM groups at 6 weeks. Scale bars, 500 μm. The higher-magnification images of the upper row (indicated by square boxes) are listed in the second row. Scale bars, 200 μm. (B) Immunofluorescence staining images of periostin in the femur defect at 6 weeks post-surgery. Scale bars, 100 μm. Data are presented as mean ± SD. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001. P, Periosteum; C, cortical bone; DAPI, 4′,6-diamidino-2-phenylindole; OSX, Osterix; LepR, <t>leptin</t> receptor; GC, biomimetic periosteum without Func-HA and BMP-2; GC-N, biomimetic periosteum without Func-HA; GC-NB, biomimetic periosteum; CM, collagen membrane. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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    The biomimetic periosteum increases PSCs accumulation in the bone defect region and upregulates periostin expression. (A) Immunofluorescence staining of PSCs (OSX + <t>LepR</t> + osteoprogenitors, yellow) in the bone defect region of the control, GC, GC-N, GC-NB and CM groups at 6 weeks. Scale bars, 500 μm. The higher-magnification images of the upper row (indicated by square boxes) are listed in the second row. Scale bars, 200 μm. (B) Immunofluorescence staining images of periostin in the femur defect at 6 weeks post-surgery. Scale bars, 100 μm. Data are presented as mean ± SD. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001. P, Periosteum; C, cortical bone; DAPI, 4′,6-diamidino-2-phenylindole; OSX, Osterix; LepR, <t>leptin</t> receptor; GC, biomimetic periosteum without Func-HA and BMP-2; GC-N, biomimetic periosteum without Func-HA; GC-NB, biomimetic periosteum; CM, collagen membrane. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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    The biomimetic periosteum increases PSCs accumulation in the bone defect region and upregulates periostin expression. (A) Immunofluorescence staining of PSCs (OSX + <t>LepR</t> + osteoprogenitors, yellow) in the bone defect region of the control, GC, GC-N, GC-NB and CM groups at 6 weeks. Scale bars, 500 μm. The higher-magnification images of the upper row (indicated by square boxes) are listed in the second row. Scale bars, 200 μm. (B) Immunofluorescence staining images of periostin in the femur defect at 6 weeks post-surgery. Scale bars, 100 μm. Data are presented as mean ± SD. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001. P, Periosteum; C, cortical bone; DAPI, 4′,6-diamidino-2-phenylindole; OSX, Osterix; LepR, <t>leptin</t> receptor; GC, biomimetic periosteum without Func-HA and BMP-2; GC-N, biomimetic periosteum without Func-HA; GC-NB, biomimetic periosteum; CM, collagen membrane. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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    The biomimetic periosteum increases PSCs accumulation in the bone defect region and upregulates periostin expression. (A) Immunofluorescence staining of PSCs (OSX + <t>LepR</t> + osteoprogenitors, yellow) in the bone defect region of the control, GC, GC-N, GC-NB and CM groups at 6 weeks. Scale bars, 500 μm. The higher-magnification images of the upper row (indicated by square boxes) are listed in the second row. Scale bars, 200 μm. (B) Immunofluorescence staining images of periostin in the femur defect at 6 weeks post-surgery. Scale bars, 100 μm. Data are presented as mean ± SD. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001. P, Periosteum; C, cortical bone; DAPI, 4′,6-diamidino-2-phenylindole; OSX, Osterix; LepR, <t>leptin</t> receptor; GC, biomimetic periosteum without Func-HA and BMP-2; GC-N, biomimetic periosteum without Func-HA; GC-NB, biomimetic periosteum; CM, collagen membrane. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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    List of primary and secondary antibodies: sources and product models
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    Image Search Results


    Experimental validation supports a senescence-associated role of LEP in EOPE. (A) qRT–PCR analysis of LEP, ENG, MIF and CYBB mRNA expression in PTB and EOPE placentas. n = 6 biologically independent placentas per group. Bars represent mean ± SD. (B) Representative images of senescence-associated β-galactosidase (SA-β-gal) staining. (C) Representative immunofluorescence images of P21 in PTB and EOPE placentas. Nuclei were counterstained with Hoechst. (D) Representative images of LEP immunohistochemistry in PTB and EOPE placentas. Scale bars, 100 μm. n = 6 biologically independent placentas per group. (E) Representative western blot showing LEP protein expression in PTB and EOPE placentas. n = 6. (F) Western blot analysis of P21 and LEP protein expression in BeWo cells treated with increasing concentrations of leptin. (G) Representative SA-β-gal staining images (left) and quantification of SA-β-gal-positive cells (right) in BeWo cells treated with leptin. n = 3 biologically independent experiments. Bars represent mean ± SD. (H) Detection of hCG in cell culture supernatant by ELISA after 24 h of leptin treatment.

    Journal: Frontiers in Endocrinology

    Article Title: Integrative bioinformatics analysis identifies placental senescence-associated signatures in early-onset preeclampsia

    doi: 10.3389/fendo.2026.1863608

    Figure Lengend Snippet: Experimental validation supports a senescence-associated role of LEP in EOPE. (A) qRT–PCR analysis of LEP, ENG, MIF and CYBB mRNA expression in PTB and EOPE placentas. n = 6 biologically independent placentas per group. Bars represent mean ± SD. (B) Representative images of senescence-associated β-galactosidase (SA-β-gal) staining. (C) Representative immunofluorescence images of P21 in PTB and EOPE placentas. Nuclei were counterstained with Hoechst. (D) Representative images of LEP immunohistochemistry in PTB and EOPE placentas. Scale bars, 100 μm. n = 6 biologically independent placentas per group. (E) Representative western blot showing LEP protein expression in PTB and EOPE placentas. n = 6. (F) Western blot analysis of P21 and LEP protein expression in BeWo cells treated with increasing concentrations of leptin. (G) Representative SA-β-gal staining images (left) and quantification of SA-β-gal-positive cells (right) in BeWo cells treated with leptin. n = 3 biologically independent experiments. Bars represent mean ± SD. (H) Detection of hCG in cell culture supernatant by ELISA after 24 h of leptin treatment.

    Article Snippet: The obtained placental tissue sections were incubated overnight at 4 °C in a humidified incubation chamber with the primary antibody: anti-rabbit leptin (A1300, ABclonal).

    Techniques: Biomarker Discovery, Quantitative RT-PCR, Expressing, Staining, Immunofluorescence, Immunohistochemistry, Western Blot, Cell Culture, Enzyme-linked Immunosorbent Assay

    The biomimetic periosteum increases PSCs accumulation in the bone defect region and upregulates periostin expression. (A) Immunofluorescence staining of PSCs (OSX + LepR + osteoprogenitors, yellow) in the bone defect region of the control, GC, GC-N, GC-NB and CM groups at 6 weeks. Scale bars, 500 μm. The higher-magnification images of the upper row (indicated by square boxes) are listed in the second row. Scale bars, 200 μm. (B) Immunofluorescence staining images of periostin in the femur defect at 6 weeks post-surgery. Scale bars, 100 μm. Data are presented as mean ± SD. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001. P, Periosteum; C, cortical bone; DAPI, 4′,6-diamidino-2-phenylindole; OSX, Osterix; LepR, leptin receptor; GC, biomimetic periosteum without Func-HA and BMP-2; GC-N, biomimetic periosteum without Func-HA; GC-NB, biomimetic periosteum; CM, collagen membrane. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

    Journal: Materials Today Bio

    Article Title: Reverse biogradient biomimetic periosteum with osteogenic and angiogenic characteristics for bone regeneration

    doi: 10.1016/j.mtbio.2025.101967

    Figure Lengend Snippet: The biomimetic periosteum increases PSCs accumulation in the bone defect region and upregulates periostin expression. (A) Immunofluorescence staining of PSCs (OSX + LepR + osteoprogenitors, yellow) in the bone defect region of the control, GC, GC-N, GC-NB and CM groups at 6 weeks. Scale bars, 500 μm. The higher-magnification images of the upper row (indicated by square boxes) are listed in the second row. Scale bars, 200 μm. (B) Immunofluorescence staining images of periostin in the femur defect at 6 weeks post-surgery. Scale bars, 100 μm. Data are presented as mean ± SD. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001. P, Periosteum; C, cortical bone; DAPI, 4′,6-diamidino-2-phenylindole; OSX, Osterix; LepR, leptin receptor; GC, biomimetic periosteum without Func-HA and BMP-2; GC-N, biomimetic periosteum without Func-HA; GC-NB, biomimetic periosteum; CM, collagen membrane. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: Furthermore, decalcified femoral sections were incubated with antibodies against CD31 (Abcam, 1:500), Osterix (OSX, Abcam, 1:500), periostin (Abcam, 1:500), α-smooth muscle actin (αSMA, Service, 1:200), endomucin (Emcn, Service, 1:200) and leptin receptor (LepR, ABclonal, 1:200) overnight at 4 °C, followed by incubation with biotinylated secondary antibodies or fluorophore-conjugated secondary antibodies in the dark.

    Techniques: Expressing, Immunofluorescence, Staining, Control, Membrane

    List of primary and secondary antibodies: sources and product models

    Journal: Iranian Journal of Basic Medical Sciences

    Article Title: Effects of different pre-conditioning exercise on leptin synthesis and its downstream signalling pathway in T2DM rats

    doi: 10.22038/ijbms.2024.77774.16828

    Figure Lengend Snippet: List of primary and secondary antibodies: sources and product models

    Article Snippet: Rabbit anti-Leptin , Boster Biological Technology , BA1231.

    Techniques: