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alp staining solution  (Vector Laboratories)


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    Vector Laboratories alp staining solution
    Alp Staining Solution, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1935 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/alp+substrate+solution/VECTOR+Red+Alkaline+Phosphatase+(Red+AP)+Substrate+Kit/pm38416823-357-26-29
    Average 96 stars, based on 1935 article reviews
    alp staining solution - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Staining:

    Article Title: The IQGAP1-Claudin4-JNK Signaling Axis as a Differential Biomarker in Renal Cell Carcinoma.
    Article Snippet: The sections were developed using the 3,3′- diaminobenzidine (DAB) substrate for 5 min (SPlink HRP Rabbit Detection (DAB) kit, cat. no. D- 03- 18; OriGene Technologies Inc.) and counterstained with hematoxylin QS (H- 3404, Vector Laboratories). .. For IQGAP1- Claudin doublestaining, IQGAP1 was stained red/magenta using ImmPACT Vector Red Substrate Kit, Alkaline Phosphatase (SK- 5105), and claudin was stained brown using Vectastain Elite ABC Universal kit, Peroxidase (PK- 7200). .. The images were captured using an Olympus microscope.

    Article Title: The IQGAP1 ‐Claudin4‐ JNK Signaling Axis as a Differential Biomarker in Renal Cell Carcinoma
    Article Snippet: The sections were developed using the 3,3′‐diaminobenzidine (DAB) substrate for 5 min (SPlink HRP Rabbit Detection (DAB) kit, cat. no. D‐03‐18; OriGene Technologies Inc.) and counterstained with hematoxylin QS (H‐3404, Vector Laboratories). .. For IQGAP1‐Claudin double‐staining, IQGAP1 was stained red/magenta using ImmPACT Vector Red Substrate Kit, Alkaline Phosphatase (SK‐5105), and claudin was stained brown using Vectastain Elite ABC Universal kit, Peroxidase (PK‐7200). .. The images were captured using an Olympus microscope.

    other:

    Article Title: The nuclear cap-binding complex safeguards stress-resistant protein synthesis and proliferation of stem cells
    Article Snippet: For NE differentiation, hESCs were cultured on Matrigel-coated plates in an hESC medium (DMEM/F12 supplemented with 15% knockout serum replacement, minimum essential medium nonessential amino acids and 0.1 mM 2-mercaptoethanol) added with 10 μM SB431542 (PeproTech) and 2 μM dorsomorphin (Tocris) via the dual SMAD inhibition method.

    ALP Assay:

    Article Title: The nuclear cap-binding complex safeguards stress-resistant protein synthesis and proliferation of stem cells
    Article Snippet: .. Reprogrammed iPSC colonies were fixed with 4% paraformaldehyde for 15 min and subjected to an alkaline phosphatase assay by using the Vector Red Alkaline Phosphatase Substrate Kit I (Vector laboratories). .. HEK293T cells were transfected with the indicated plasmids using either the calcium phosphate method or Lipofectamine 2000 (Invitrogen).

    Incubation:

    Article Title: A chlorhexidine-releasing epoxy-based coating on titanium implants prevents Staphylococcus aureus experimental biomaterial-associated infection
    Article Snippet: .. Next, sections were incubated with 1: 10000 diluted rabbit anti-S. aureus polyclonal IgG (20920, Abcam) for 1 h at RT, with undiluted BrightVision anti-rabbit AP for 30 min at RT and with Vector Red (SK-5100, Vector Labs) for 10 min at RT, again with three TBS washes between all incubations. .. After another HIER-citrate (10 min at 98 °C) and Superblock incubation, sections were incubated with 1: 1000 diluted rat anti-mouse Ly-6G-FITC (neutrophils; 553126, BD) in TBS for 2 h at RT, with 1: 1000 diluted rabbit anti-FITC (4510-7804, Nuclilab) in the presence of 5 % normal mouse serum in TBS for 15 min at RT, with undiluted BrightVision anti-rabbit IgG-HRP (DPVR110HRP, Immunologic) for 30 min at RT, and finally stained for ~8 min with DAB (BS04-110, Immunologic) until they turned yellow/brownish.

    Transcranial Magnetic Stimulation:

    Article Title: A chlorhexidine-releasing epoxy-based coating on titanium implants prevents Staphylococcus aureus experimental biomaterial-associated infection
    Article Snippet: .. Next, sections were incubated with 1: 10000 diluted rabbit anti-S. aureus polyclonal IgG (20920, Abcam) for 1 h at RT, with undiluted BrightVision anti-rabbit AP for 30 min at RT and with Vector Red (SK-5100, Vector Labs) for 10 min at RT, again with three TBS washes between all incubations. .. After another HIER-citrate (10 min at 98 °C) and Superblock incubation, sections were incubated with 1: 1000 diluted rat anti-mouse Ly-6G-FITC (neutrophils; 553126, BD) in TBS for 2 h at RT, with 1: 1000 diluted rabbit anti-FITC (4510-7804, Nuclilab) in the presence of 5 % normal mouse serum in TBS for 15 min at RT, with undiluted BrightVision anti-rabbit IgG-HRP (DPVR110HRP, Immunologic) for 30 min at RT, and finally stained for ~8 min with DAB (BS04-110, Immunologic) until they turned yellow/brownish.

    Double Staining:

    Article Title: The IQGAP1 ‐Claudin4‐ JNK Signaling Axis as a Differential Biomarker in Renal Cell Carcinoma
    Article Snippet: The sections were developed using the 3,3′‐diaminobenzidine (DAB) substrate for 5 min (SPlink HRP Rabbit Detection (DAB) kit, cat. no. D‐03‐18; OriGene Technologies Inc.) and counterstained with hematoxylin QS (H‐3404, Vector Laboratories). .. For IQGAP1‐Claudin double‐staining, IQGAP1 was stained red/magenta using ImmPACT Vector Red Substrate Kit, Alkaline Phosphatase (SK‐5105), and claudin was stained brown using Vectastain Elite ABC Universal kit, Peroxidase (PK‐7200). .. The images were captured using an Olympus microscope.



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    FIGURE 4 Thunnus orientalis, distribution of osteoblasts and osteoclasts in vertebrae. (a) Double staining of <t>ALP</t> and TRAP of a juvenile vertebral body. The total length of the juvenile of (a) is 11.2 cm. (b–d) Magnified images of (b) the lateral ridge, (c) the base of the dorsal arch, and (d) the base of the hemal arch base marked with rectangles in (a). Arrows and arrowheads indicate ALP‐positive osteoblasts and TRAP‐positive osteoclasts, respectively. (e) HE and alcian blue staining of a lateral ridge of an adult vertebra. (f, g) Magnified images of (f) the distal edge and (g) the surface of the lateral ridge marked with rectangles in (e). (f) Black‐filled arrowheads indicate osteoblasts accumulating on the edge of the ridge. Asterisks indicate the small cavities in which osteoblasts are embedded. Branches from black circles indicate osteocyte lacunae. The cavities are much larger than the osteocyte lacunae. (g) The arrowhead indicates osteoblasts lined up along the surface of the ridge. No alcian‐ blue‐positive cartilage was observed. Scale bars: (a–d) 100 µm, (e) 500 µm, and (f, g) 50 µm. ALP, alkaline <t>phosphatase;</t> bv, blood vessel; HE, hematoxylin and eosin; sc, spinal cord; TRAP, tartrate‐resistant acid phosphatase.
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    FIGURE 4 Thunnus orientalis, distribution of osteoblasts and osteoclasts in vertebrae. (a) Double staining of <t>ALP</t> and TRAP of a juvenile vertebral body. The total length of the juvenile of (a) is 11.2 cm. (b–d) Magnified images of (b) the lateral ridge, (c) the base of the dorsal arch, and (d) the base of the hemal arch base marked with rectangles in (a). Arrows and arrowheads indicate ALP‐positive osteoblasts and TRAP‐positive osteoclasts, respectively. (e) HE and alcian blue staining of a lateral ridge of an adult vertebra. (f, g) Magnified images of (f) the distal edge and (g) the surface of the lateral ridge marked with rectangles in (e). (f) Black‐filled arrowheads indicate osteoblasts accumulating on the edge of the ridge. Asterisks indicate the small cavities in which osteoblasts are embedded. Branches from black circles indicate osteocyte lacunae. The cavities are much larger than the osteocyte lacunae. (g) The arrowhead indicates osteoblasts lined up along the surface of the ridge. No alcian‐ blue‐positive cartilage was observed. Scale bars: (a–d) 100 µm, (e) 500 µm, and (f, g) 50 µm. ALP, alkaline <t>phosphatase;</t> bv, blood vessel; HE, hematoxylin and eosin; sc, spinal cord; TRAP, tartrate‐resistant acid phosphatase.
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    Image Search Results


    Histological evaluations using ALP and ARS staining for cultured cells on fabricated ceramics. ( a ) ALP staining for cultured specimens using a bone differentiation induction medium for 1–2 weeks after preculture. ARS staining ( b ) without and ( c ) with a bone differentiation induction medium for 1–2 weeks after preculture.

    Journal: International Journal of Molecular Sciences

    Article Title: Preferred Orientation of Hydroxyapatite Ceramics Along the c -Axis Promotes Osteoblast Differentiation

    doi: 10.3390/ijms252312926

    Figure Lengend Snippet: Histological evaluations using ALP and ARS staining for cultured cells on fabricated ceramics. ( a ) ALP staining for cultured specimens using a bone differentiation induction medium for 1–2 weeks after preculture. ARS staining ( b ) without and ( c ) with a bone differentiation induction medium for 1–2 weeks after preculture.

    Article Snippet: For ALP staining, the cells were incubated with ALP substrate solution (Wako Pure Chemical Industries, Osaka, Japan) in an incubator at 37 °C for 30 min. Then, the cells were washed with sterile water and observed.

    Techniques: Staining, Cell Culture

    FIGURE 4 Thunnus orientalis, distribution of osteoblasts and osteoclasts in vertebrae. (a) Double staining of ALP and TRAP of a juvenile vertebral body. The total length of the juvenile of (a) is 11.2 cm. (b–d) Magnified images of (b) the lateral ridge, (c) the base of the dorsal arch, and (d) the base of the hemal arch base marked with rectangles in (a). Arrows and arrowheads indicate ALP‐positive osteoblasts and TRAP‐positive osteoclasts, respectively. (e) HE and alcian blue staining of a lateral ridge of an adult vertebra. (f, g) Magnified images of (f) the distal edge and (g) the surface of the lateral ridge marked with rectangles in (e). (f) Black‐filled arrowheads indicate osteoblasts accumulating on the edge of the ridge. Asterisks indicate the small cavities in which osteoblasts are embedded. Branches from black circles indicate osteocyte lacunae. The cavities are much larger than the osteocyte lacunae. (g) The arrowhead indicates osteoblasts lined up along the surface of the ridge. No alcian‐ blue‐positive cartilage was observed. Scale bars: (a–d) 100 µm, (e) 500 µm, and (f, g) 50 µm. ALP, alkaline phosphatase; bv, blood vessel; HE, hematoxylin and eosin; sc, spinal cord; TRAP, tartrate‐resistant acid phosphatase.

    Journal: Journal of morphology

    Article Title: Lateral bone ridge expansion and internal tissue replacement for vertebral body growth in Pacific bluefin tuna Thunnus orientalis.

    doi: 10.1002/jmor.21666

    Figure Lengend Snippet: FIGURE 4 Thunnus orientalis, distribution of osteoblasts and osteoclasts in vertebrae. (a) Double staining of ALP and TRAP of a juvenile vertebral body. The total length of the juvenile of (a) is 11.2 cm. (b–d) Magnified images of (b) the lateral ridge, (c) the base of the dorsal arch, and (d) the base of the hemal arch base marked with rectangles in (a). Arrows and arrowheads indicate ALP‐positive osteoblasts and TRAP‐positive osteoclasts, respectively. (e) HE and alcian blue staining of a lateral ridge of an adult vertebra. (f, g) Magnified images of (f) the distal edge and (g) the surface of the lateral ridge marked with rectangles in (e). (f) Black‐filled arrowheads indicate osteoblasts accumulating on the edge of the ridge. Asterisks indicate the small cavities in which osteoblasts are embedded. Branches from black circles indicate osteocyte lacunae. The cavities are much larger than the osteocyte lacunae. (g) The arrowhead indicates osteoblasts lined up along the surface of the ridge. No alcian‐ blue‐positive cartilage was observed. Scale bars: (a–d) 100 µm, (e) 500 µm, and (f, g) 50 µm. ALP, alkaline phosphatase; bv, blood vessel; HE, hematoxylin and eosin; sc, spinal cord; TRAP, tartrate‐resistant acid phosphatase.

    Article Snippet: To detect osteoblasts, we mounted 100 μL alkaline phosphatase (ALP) substrate solution (Takara) and incubated the sections for 20min at 37°C.

    Techniques: Double Staining, Staining

    FIGURE 5 Thunnus orientalis, osteoblasts in the small cavities of vertebrae. (a) Schematic illustration showing the positions of the slices (b–d) in vertebrae. (b–d) Double staining of ALP and TRAP of the vertebrae of the juveniles. Green lines in (b–d) indicate the outline of the bones, which correspond to that of (a). Arrows indicate the direction of osteoblast alignment. (b) The lateral part of an hourglass‐shaped bone from which the lateral ridge extends. Osteoblasts are embedded in the small cavities, and the direction of osteoblasts is circular in the hourglass‐shaped parts and lateral in the lateral ridge. No osteoclasts are observed in the small cavities. Arrowheads indicate osteoclasts forming bone marrow cavities. (c) The distal end of the lateral ridge. Osteoblasts are laterally aligned in the distal region of the lateral ridge, and the alignments are nearly parallel. (d) Neural arch. Osteoblasts are arranged radially toward the dorsal side. The total length of juveniles of (b, c) is 39 cm, and (d) is 20 cm. Scale bars: 500 µm. ALP, alkaline phosphatase; sc, spinal cord; TRAP, tartrate‐resistant acid phosphatase.

    Journal: Journal of morphology

    Article Title: Lateral bone ridge expansion and internal tissue replacement for vertebral body growth in Pacific bluefin tuna Thunnus orientalis.

    doi: 10.1002/jmor.21666

    Figure Lengend Snippet: FIGURE 5 Thunnus orientalis, osteoblasts in the small cavities of vertebrae. (a) Schematic illustration showing the positions of the slices (b–d) in vertebrae. (b–d) Double staining of ALP and TRAP of the vertebrae of the juveniles. Green lines in (b–d) indicate the outline of the bones, which correspond to that of (a). Arrows indicate the direction of osteoblast alignment. (b) The lateral part of an hourglass‐shaped bone from which the lateral ridge extends. Osteoblasts are embedded in the small cavities, and the direction of osteoblasts is circular in the hourglass‐shaped parts and lateral in the lateral ridge. No osteoclasts are observed in the small cavities. Arrowheads indicate osteoclasts forming bone marrow cavities. (c) The distal end of the lateral ridge. Osteoblasts are laterally aligned in the distal region of the lateral ridge, and the alignments are nearly parallel. (d) Neural arch. Osteoblasts are arranged radially toward the dorsal side. The total length of juveniles of (b, c) is 39 cm, and (d) is 20 cm. Scale bars: 500 µm. ALP, alkaline phosphatase; sc, spinal cord; TRAP, tartrate‐resistant acid phosphatase.

    Article Snippet: To detect osteoblasts, we mounted 100 μL alkaline phosphatase (ALP) substrate solution (Takara) and incubated the sections for 20min at 37°C.

    Techniques: Double Staining