Review



s haemolyticus  (DSMZ)


Bioz Verified Symbol DSMZ is a verified supplier  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 95

    Structured Review

    DSMZ s haemolyticus
    Trend of LA MIC changes for S. <t>haemolyticus</t> during sub-inhibitory treatment.
    S Haemolyticus, supplied by DSMZ, used in various techniques. Bioz Stars score: 95/100, based on 80 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/acc/pmc12991841-125-6-23?v=DSMZ
    Average 95 stars, based on 80 article reviews
    s haemolyticus - by Bioz Stars, 2026-06
    95/100 stars

    Images

    1) Product Images from "Aerococcus viridans, Staphylococcus haemolyticus and Corynebacterium bovis : sub-inhibitory exposure of lactic acid and cross-resistance to β-lactams antibiotics"

    Article Title: Aerococcus viridans, Staphylococcus haemolyticus and Corynebacterium bovis : sub-inhibitory exposure of lactic acid and cross-resistance to β-lactams antibiotics

    Journal: Veterinary and Animal Science

    doi: 10.1016/j.vas.2026.100620

    Trend of LA MIC changes for S. haemolyticus during sub-inhibitory treatment.
    Figure Legend Snippet: Trend of LA MIC changes for S. haemolyticus during sub-inhibitory treatment.

    Techniques Used:

    Correlation of LA and ꞵ-lactam antibiotic* tolerance between pre- and post-exposure in S. haemolyticus . Tolerance compared in measured MIC steps (+1). ▼ = 1 step decrease from the initial MIC. One MIC-step equals to a 2-fold change in antibiotic MICs and a 1.3-fold change in LA MICs. *Cefquinome, penicillin + novobiocin, and amoxicillin + clavulanic acid showed no changes at all.
    Figure Legend Snippet: Correlation of LA and ꞵ-lactam antibiotic* tolerance between pre- and post-exposure in S. haemolyticus . Tolerance compared in measured MIC steps (+1). ▼ = 1 step decrease from the initial MIC. One MIC-step equals to a 2-fold change in antibiotic MICs and a 1.3-fold change in LA MICs. *Cefquinome, penicillin + novobiocin, and amoxicillin + clavulanic acid showed no changes at all.

    Techniques Used:



    Similar Products

    99
    ATCC mcf7 acc 115 breast carcinoma
    Mcf7 Acc 115 Breast Carcinoma, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/acc/10__20517_slash_cdr__2025__203-71-57-72?v=ATCC
    Average 99 stars, based on 1 article reviews
    mcf7 acc 115 breast carcinoma - by Bioz Stars, 2026-06
    99/100 stars
      Buy from Supplier

    94
    Alomone Labs anti trpm4 antibody
    Generation of <t>Trpm4</t> -knockout mouse line. A. Map of the mouse Trpm4 locus showing exons 15 and 16 targeted for deletion by sgRNAs. Top, WT allele. Bottom, KO allele. The sgRNAs were designed to target introns 14 and 16 flanking exons 15 and 16. Specific primers for amplifying the WT(Fw2/Rv) or KO (Fw1/Rv) allele were used. B. A representative result of genotyping PCR using a mixture of the Fw1, Fw2, and Rv primers. Two fragments were amplified from heterozygote mouse samples, each indicating the WT or KO fragment. The bottom fragment (695 bp) was amplified using the WT primer pair. The top fragment (928 bp) was amplified using the KO primer pair, indicating successful deletion of exons 15 and 16, which was confirmed by direct sequencing. (C and D). The expression patterns of Trpm4 gene in mouse brain (C) or primary microglia (D) using Gapdh as a control. In (C), “M4-plasmid” indicates an amplified fragment using mouse TRPM4 plasmid as a template. E. Western blot analysis of Trpm4 in mouse TRPM4-expressing HEK293T cells (M4-HEK) and mouse colon samples from WT or TRPM4KO mice. The expected molecular weight of Trpm4 is 134 kDa.
    Anti Trpm4 Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/acc/pmc12999298-64-22-26?v=Alomone+Labs
    Average 94 stars, based on 1 article reviews
    anti trpm4 antibody - by Bioz Stars, 2026-06
    94/100 stars
      Buy from Supplier

    86
    Medicago acc synthases
    Generation of <t>Trpm4</t> -knockout mouse line. A. Map of the mouse Trpm4 locus showing exons 15 and 16 targeted for deletion by sgRNAs. Top, WT allele. Bottom, KO allele. The sgRNAs were designed to target introns 14 and 16 flanking exons 15 and 16. Specific primers for amplifying the WT(Fw2/Rv) or KO (Fw1/Rv) allele were used. B. A representative result of genotyping PCR using a mixture of the Fw1, Fw2, and Rv primers. Two fragments were amplified from heterozygote mouse samples, each indicating the WT or KO fragment. The bottom fragment (695 bp) was amplified using the WT primer pair. The top fragment (928 bp) was amplified using the KO primer pair, indicating successful deletion of exons 15 and 16, which was confirmed by direct sequencing. (C and D). The expression patterns of Trpm4 gene in mouse brain (C) or primary microglia (D) using Gapdh as a control. In (C), “M4-plasmid” indicates an amplified fragment using mouse TRPM4 plasmid as a template. E. Western blot analysis of Trpm4 in mouse TRPM4-expressing HEK293T cells (M4-HEK) and mouse colon samples from WT or TRPM4KO mice. The expected molecular weight of Trpm4 is 134 kDa.
    Acc Synthases, supplied by Medicago, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/acc/pm42267652-58-7-2?v=Medicago
    Average 86 stars, based on 1 article reviews
    acc synthases - by Bioz Stars, 2026-06
    86/100 stars
      Buy from Supplier

    86
    Kodak acc 5092 10 fabric
    Generation of <t>Trpm4</t> -knockout mouse line. A. Map of the mouse Trpm4 locus showing exons 15 and 16 targeted for deletion by sgRNAs. Top, WT allele. Bottom, KO allele. The sgRNAs were designed to target introns 14 and 16 flanking exons 15 and 16. Specific primers for amplifying the WT(Fw2/Rv) or KO (Fw1/Rv) allele were used. B. A representative result of genotyping PCR using a mixture of the Fw1, Fw2, and Rv primers. Two fragments were amplified from heterozygote mouse samples, each indicating the WT or KO fragment. The bottom fragment (695 bp) was amplified using the WT primer pair. The top fragment (928 bp) was amplified using the KO primer pair, indicating successful deletion of exons 15 and 16, which was confirmed by direct sequencing. (C and D). The expression patterns of Trpm4 gene in mouse brain (C) or primary microglia (D) using Gapdh as a control. In (C), “M4-plasmid” indicates an amplified fragment using mouse TRPM4 plasmid as a template. E. Western blot analysis of Trpm4 in mouse TRPM4-expressing HEK293T cells (M4-HEK) and mouse colon samples from WT or TRPM4KO mice. The expected molecular weight of Trpm4 is 134 kDa.
    Acc 5092 10 Fabric, supplied by Kodak, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/acc/pm42243468-127-12-7?v=Kodak
    Average 86 stars, based on 1 article reviews
    acc 5092 10 fabric - by Bioz Stars, 2026-06
    86/100 stars
      Buy from Supplier

    96
    Alomone Labs anti-cav1.2 (cacna1c) antibody
    Generation of <t>Trpm4</t> -knockout mouse line. A. Map of the mouse Trpm4 locus showing exons 15 and 16 targeted for deletion by sgRNAs. Top, WT allele. Bottom, KO allele. The sgRNAs were designed to target introns 14 and 16 flanking exons 15 and 16. Specific primers for amplifying the WT(Fw2/Rv) or KO (Fw1/Rv) allele were used. B. A representative result of genotyping PCR using a mixture of the Fw1, Fw2, and Rv primers. Two fragments were amplified from heterozygote mouse samples, each indicating the WT or KO fragment. The bottom fragment (695 bp) was amplified using the WT primer pair. The top fragment (928 bp) was amplified using the KO primer pair, indicating successful deletion of exons 15 and 16, which was confirmed by direct sequencing. (C and D). The expression patterns of Trpm4 gene in mouse brain (C) or primary microglia (D) using Gapdh as a control. In (C), “M4-plasmid” indicates an amplified fragment using mouse TRPM4 plasmid as a template. E. Western blot analysis of Trpm4 in mouse TRPM4-expressing HEK293T cells (M4-HEK) and mouse colon samples from WT or TRPM4KO mice. The expected molecular weight of Trpm4 is 134 kDa.
    Anti Cav1.2 (Cacna1c) Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/acc/alomone+labs___acc-003?v=Alomone+Labs
    Average 96 stars, based on 1 article reviews
    anti-cav1.2 (cacna1c) antibody - by Bioz Stars, 2026-06
    96/100 stars
      Buy from Supplier

    95
    DSMZ s haemolyticus
    Trend of LA MIC changes for S. <t>haemolyticus</t> during sub-inhibitory treatment.
    S Haemolyticus, supplied by DSMZ, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/acc/pmc12991841-125-6-23?v=DSMZ
    Average 95 stars, based on 1 article reviews
    s haemolyticus - by Bioz Stars, 2026-06
    95/100 stars
      Buy from Supplier

    86
    Novogene anterior cingulate cortex acc
    Trend of LA MIC changes for S. <t>haemolyticus</t> during sub-inhibitory treatment.
    Anterior Cingulate Cortex Acc, supplied by Novogene, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/acc/pm42134517-83-13-28?v=Novogene
    Average 86 stars, based on 1 article reviews
    anterior cingulate cortex acc - by Bioz Stars, 2026-06
    86/100 stars
      Buy from Supplier

    93
    Alomone Labs anti-ip3 receptor-2 antibody
    Trend of LA MIC changes for S. <t>haemolyticus</t> during sub-inhibitory treatment.
    Anti Ip3 Receptor 2 Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/acc/alomone+labs___acc-116?v=Alomone+Labs
    Average 93 stars, based on 1 article reviews
    anti-ip3 receptor-2 antibody - by Bioz Stars, 2026-06
    93/100 stars
      Buy from Supplier

    95
    Alomone Labs anti cav1 3
    Trend of LA MIC changes for S. <t>haemolyticus</t> during sub-inhibitory treatment.
    Anti Cav1 3, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/acc/pmc13123447-54-33-35?v=Alomone+Labs
    Average 95 stars, based on 1 article reviews
    anti cav1 3 - by Bioz Stars, 2026-06
    95/100 stars
      Buy from Supplier

    Image Search Results


    Generation of Trpm4 -knockout mouse line. A. Map of the mouse Trpm4 locus showing exons 15 and 16 targeted for deletion by sgRNAs. Top, WT allele. Bottom, KO allele. The sgRNAs were designed to target introns 14 and 16 flanking exons 15 and 16. Specific primers for amplifying the WT(Fw2/Rv) or KO (Fw1/Rv) allele were used. B. A representative result of genotyping PCR using a mixture of the Fw1, Fw2, and Rv primers. Two fragments were amplified from heterozygote mouse samples, each indicating the WT or KO fragment. The bottom fragment (695 bp) was amplified using the WT primer pair. The top fragment (928 bp) was amplified using the KO primer pair, indicating successful deletion of exons 15 and 16, which was confirmed by direct sequencing. (C and D). The expression patterns of Trpm4 gene in mouse brain (C) or primary microglia (D) using Gapdh as a control. In (C), “M4-plasmid” indicates an amplified fragment using mouse TRPM4 plasmid as a template. E. Western blot analysis of Trpm4 in mouse TRPM4-expressing HEK293T cells (M4-HEK) and mouse colon samples from WT or TRPM4KO mice. The expected molecular weight of Trpm4 is 134 kDa.

    Journal: The Journal of Physiological Sciences : JPS

    Article Title: Genetic inactivation of TRPM4 does not alter the temperature-dependent movement of mouse microglia

    doi: 10.1016/j.jphyss.2026.100067

    Figure Lengend Snippet: Generation of Trpm4 -knockout mouse line. A. Map of the mouse Trpm4 locus showing exons 15 and 16 targeted for deletion by sgRNAs. Top, WT allele. Bottom, KO allele. The sgRNAs were designed to target introns 14 and 16 flanking exons 15 and 16. Specific primers for amplifying the WT(Fw2/Rv) or KO (Fw1/Rv) allele were used. B. A representative result of genotyping PCR using a mixture of the Fw1, Fw2, and Rv primers. Two fragments were amplified from heterozygote mouse samples, each indicating the WT or KO fragment. The bottom fragment (695 bp) was amplified using the WT primer pair. The top fragment (928 bp) was amplified using the KO primer pair, indicating successful deletion of exons 15 and 16, which was confirmed by direct sequencing. (C and D). The expression patterns of Trpm4 gene in mouse brain (C) or primary microglia (D) using Gapdh as a control. In (C), “M4-plasmid” indicates an amplified fragment using mouse TRPM4 plasmid as a template. E. Western blot analysis of Trpm4 in mouse TRPM4-expressing HEK293T cells (M4-HEK) and mouse colon samples from WT or TRPM4KO mice. The expected molecular weight of Trpm4 is 134 kDa.

    Article Snippet: After transferring the proteins to a nitrocellulose membrane, the membrane was blocked for 1 h at room temperature and then incubated with anti-TRPM4 antibody (1:300, ACC044, Alomone) overnight at 4 °C.

    Techniques: Knock-Out, Amplification, Sequencing, Expressing, Control, Plasmid Preparation, Western Blot, Molecular Weight

    Genetic elimination of Trpm4 does not alter the temperature-dependent microglia movement. A. Trajectories of primary microglia from a representative preparation of WT and TRPM4KO mice recorded for 2 h at 33 °C, 37 °C, and 40 °C. Paths are arranged to show origins at x (horizontal axis) = y (vertical axis) = 0. Each line indicates the trajectory of a single cell. n indicates the number of cells analyzed per preparation. B. The average distances of migrating microglia isolated from WT or TRPM4KO mice exposed to 33 °C (WT, n = 117; TRPM4KO, n = 151), 37 °C (WT, n = 235; TRPM4KO, n = 240), or 40 °C (WT, n = 150; TRPM4KO, n = 175) were measured. Open circles indicate the migration distance of each microglia over 2 h. Horizontal lines indicate means ± SEM. At 33 °C, 37 °C, and 40 °C, WT microglia moved 112.94 ± 6.1 μm, 175.28 ± 5.24 μm, and 204.31 ± 7.27 μm, respectively, whereas TRPM4KO microglia moved 113.46 ± 5.1 μm, 175.28 ± 4.13 μm, and 201.35 ± 5.61 μm, respectively. **P < 0.01 (two-way ANOVA followed by post hoc Bonferroni test for multiple comparisons).

    Journal: The Journal of Physiological Sciences : JPS

    Article Title: Genetic inactivation of TRPM4 does not alter the temperature-dependent movement of mouse microglia

    doi: 10.1016/j.jphyss.2026.100067

    Figure Lengend Snippet: Genetic elimination of Trpm4 does not alter the temperature-dependent microglia movement. A. Trajectories of primary microglia from a representative preparation of WT and TRPM4KO mice recorded for 2 h at 33 °C, 37 °C, and 40 °C. Paths are arranged to show origins at x (horizontal axis) = y (vertical axis) = 0. Each line indicates the trajectory of a single cell. n indicates the number of cells analyzed per preparation. B. The average distances of migrating microglia isolated from WT or TRPM4KO mice exposed to 33 °C (WT, n = 117; TRPM4KO, n = 151), 37 °C (WT, n = 235; TRPM4KO, n = 240), or 40 °C (WT, n = 150; TRPM4KO, n = 175) were measured. Open circles indicate the migration distance of each microglia over 2 h. Horizontal lines indicate means ± SEM. At 33 °C, 37 °C, and 40 °C, WT microglia moved 112.94 ± 6.1 μm, 175.28 ± 5.24 μm, and 204.31 ± 7.27 μm, respectively, whereas TRPM4KO microglia moved 113.46 ± 5.1 μm, 175.28 ± 4.13 μm, and 201.35 ± 5.61 μm, respectively. **P < 0.01 (two-way ANOVA followed by post hoc Bonferroni test for multiple comparisons).

    Article Snippet: After transferring the proteins to a nitrocellulose membrane, the membrane was blocked for 1 h at room temperature and then incubated with anti-TRPM4 antibody (1:300, ACC044, Alomone) overnight at 4 °C.

    Techniques: Single Cell, Isolation, Migration

    Trend of LA MIC changes for S. haemolyticus during sub-inhibitory treatment.

    Journal: Veterinary and Animal Science

    Article Title: Aerococcus viridans, Staphylococcus haemolyticus and Corynebacterium bovis : sub-inhibitory exposure of lactic acid and cross-resistance to β-lactams antibiotics

    doi: 10.1016/j.vas.2026.100620

    Figure Lengend Snippet: Trend of LA MIC changes for S. haemolyticus during sub-inhibitory treatment.

    Article Snippet: Fig 5 dummy alt text While S. haemolyticus displayed a 2-fold rise of cefoperazon for 2 field isolates (4137SH and 3934SH) plus the DSMZ reference astrain, there was also a 1 step decrease for 1 isolate (3958SH).

    Techniques:

    Correlation of LA and ꞵ-lactam antibiotic* tolerance between pre- and post-exposure in S. haemolyticus . Tolerance compared in measured MIC steps (+1). ▼ = 1 step decrease from the initial MIC. One MIC-step equals to a 2-fold change in antibiotic MICs and a 1.3-fold change in LA MICs. *Cefquinome, penicillin + novobiocin, and amoxicillin + clavulanic acid showed no changes at all.

    Journal: Veterinary and Animal Science

    Article Title: Aerococcus viridans, Staphylococcus haemolyticus and Corynebacterium bovis : sub-inhibitory exposure of lactic acid and cross-resistance to β-lactams antibiotics

    doi: 10.1016/j.vas.2026.100620

    Figure Lengend Snippet: Correlation of LA and ꞵ-lactam antibiotic* tolerance between pre- and post-exposure in S. haemolyticus . Tolerance compared in measured MIC steps (+1). ▼ = 1 step decrease from the initial MIC. One MIC-step equals to a 2-fold change in antibiotic MICs and a 1.3-fold change in LA MICs. *Cefquinome, penicillin + novobiocin, and amoxicillin + clavulanic acid showed no changes at all.

    Article Snippet: Fig 5 dummy alt text While S. haemolyticus displayed a 2-fold rise of cefoperazon for 2 field isolates (4137SH and 3934SH) plus the DSMZ reference astrain, there was also a 1 step decrease for 1 isolate (3958SH).

    Techniques: