mouse anti his tag ab Search Results


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SouthernBiotech hrp conjugated mouse anti his tag antibody
E. coli cells were co-transformed with pET-AEQ for expression of aequorin and pRham. Three different versions of pRham were used: the empty vector as control (empty), the vector containing LjMLO4 CDS optimized for expression in E. coli (MLO4, 65 kDa) and a truncated version of the gene (AA 1-265, MLO4Δ, 31 kDa) mimicking the putative truncated protein in mlo4-3 L. japonicus mutant line. A) Schematic representation of the two versions of LjMLO4 expressed in E. coli. The representative image of MLO topology (modified from Kusch et al . 2016 ) highlights the missing domains in LjMLO4Δ. B) Western blot showing the expression of LjMLO4-HIS and LjMLO4Δ-HIS in E. coli cells using <t>anti-HIS</t> antibody. D-G) Ca 2+ influx after injection of 1 mM CaCl 2 represented as Ca 2+ traces along time (D), level of Ca 2+ after 2 minutes (E) and after 3 minutes (F), total Ca 2+ mobilized over time (G). Statistical analysis was conducted via Kruskal-Wallis test followed by Dunn’s post-hoc correction (only p-values < 0.1 are reported).
Hrp Conjugated Mouse Anti His Tag Antibody, supplied by SouthernBiotech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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SouthernBiotech anti his tag cat
E. coli cells were co-transformed with pET-AEQ for expression of aequorin and pRham. Three different versions of pRham were used: the empty vector as control (empty), the vector containing LjMLO4 CDS optimized for expression in E. coli (MLO4, 65 kDa) and a truncated version of the gene (AA 1-265, MLO4Δ, 31 kDa) mimicking the putative truncated protein in mlo4-3 L. japonicus mutant line. A) Schematic representation of the two versions of LjMLO4 expressed in E. coli. The representative image of MLO topology (modified from Kusch et al . 2016 ) highlights the missing domains in LjMLO4Δ. B) Western blot showing the expression of LjMLO4-HIS and LjMLO4Δ-HIS in E. coli cells using <t>anti-HIS</t> antibody. D-G) Ca 2+ influx after injection of 1 mM CaCl 2 represented as Ca 2+ traces along time (D), level of Ca 2+ after 2 minutes (E) and after 3 minutes (F), total Ca 2+ mobilized over time (G). Statistical analysis was conducted via Kruskal-Wallis test followed by Dunn’s post-hoc correction (only p-values < 0.1 are reported).
Anti His Tag Cat, supplied by SouthernBiotech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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E. coli cells were co-transformed with pET-AEQ for expression of aequorin and pRham. Three different versions of pRham were used: the empty vector as control (empty), the vector containing LjMLO4 CDS optimized for expression in E. coli (MLO4, 65 kDa) and a truncated version of the gene (AA 1-265, MLO4Δ, 31 kDa) mimicking the putative truncated protein in mlo4-3 L. japonicus mutant line. A) Schematic representation of the two versions of LjMLO4 expressed in E. coli. The representative image of MLO topology (modified from Kusch et al . 2016 ) highlights the missing domains in LjMLO4Δ. B) Western blot showing the expression of LjMLO4-HIS and LjMLO4Δ-HIS in E. coli cells using <t>anti-HIS</t> antibody. D-G) Ca 2+ influx after injection of 1 mM CaCl 2 represented as Ca 2+ traces along time (D), level of Ca 2+ after 2 minutes (E) and after 3 minutes (F), total Ca 2+ mobilized over time (G). Statistical analysis was conducted via Kruskal-Wallis test followed by Dunn’s post-hoc correction (only p-values < 0.1 are reported).
Anti His Antibody Dylight Tm 550, supplied by Rockland Immunochemicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Boster Bio mouse anti his tag mab
E. coli cells were co-transformed with pET-AEQ for expression of aequorin and pRham. Three different versions of pRham were used: the empty vector as control (empty), the vector containing LjMLO4 CDS optimized for expression in E. coli (MLO4, 65 kDa) and a truncated version of the gene (AA 1-265, MLO4Δ, 31 kDa) mimicking the putative truncated protein in mlo4-3 L. japonicus mutant line. A) Schematic representation of the two versions of LjMLO4 expressed in E. coli. The representative image of MLO topology (modified from Kusch et al . 2016 ) highlights the missing domains in LjMLO4Δ. B) Western blot showing the expression of LjMLO4-HIS and LjMLO4Δ-HIS in E. coli cells using <t>anti-HIS</t> antibody. D-G) Ca 2+ influx after injection of 1 mM CaCl 2 represented as Ca 2+ traces along time (D), level of Ca 2+ after 2 minutes (E) and after 3 minutes (F), total Ca 2+ mobilized over time (G). Statistical analysis was conducted via Kruskal-Wallis test followed by Dunn’s post-hoc correction (only p-values < 0.1 are reported).
Mouse Anti His Tag Mab, supplied by Boster Bio, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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SouthernBiotech alkaline phosphatase
E. coli cells were co-transformed with pET-AEQ for expression of aequorin and pRham. Three different versions of pRham were used: the empty vector as control (empty), the vector containing LjMLO4 CDS optimized for expression in E. coli (MLO4, 65 kDa) and a truncated version of the gene (AA 1-265, MLO4Δ, 31 kDa) mimicking the putative truncated protein in mlo4-3 L. japonicus mutant line. A) Schematic representation of the two versions of LjMLO4 expressed in E. coli. The representative image of MLO topology (modified from Kusch et al . 2016 ) highlights the missing domains in LjMLO4Δ. B) Western blot showing the expression of LjMLO4-HIS and LjMLO4Δ-HIS in E. coli cells using <t>anti-HIS</t> antibody. D-G) Ca 2+ influx after injection of 1 mM CaCl 2 represented as Ca 2+ traces along time (D), level of Ca 2+ after 2 minutes (E) and after 3 minutes (F), total Ca 2+ mobilized over time (G). Statistical analysis was conducted via Kruskal-Wallis test followed by Dunn’s post-hoc correction (only p-values < 0.1 are reported).
Alkaline Phosphatase, supplied by SouthernBiotech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Sino Biological his tag antibody hrp
E. coli cells were co-transformed with pET-AEQ for expression of aequorin and pRham. Three different versions of pRham were used: the empty vector as control (empty), the vector containing LjMLO4 CDS optimized for expression in E. coli (MLO4, 65 kDa) and a truncated version of the gene (AA 1-265, MLO4Δ, 31 kDa) mimicking the putative truncated protein in mlo4-3 L. japonicus mutant line. A) Schematic representation of the two versions of LjMLO4 expressed in E. coli. The representative image of MLO topology (modified from Kusch et al . 2016 ) highlights the missing domains in LjMLO4Δ. B) Western blot showing the expression of LjMLO4-HIS and LjMLO4Δ-HIS in E. coli cells using <t>anti-HIS</t> antibody. D-G) Ca 2+ influx after injection of 1 mM CaCl 2 represented as Ca 2+ traces along time (D), level of Ca 2+ after 2 minutes (E) and after 3 minutes (F), total Ca 2+ mobilized over time (G). Statistical analysis was conducted via Kruskal-Wallis test followed by Dunn’s post-hoc correction (only p-values < 0.1 are reported).
His Tag Antibody Hrp, supplied by Sino Biological, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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SouthernBiotech mouse antibodies
E. coli cells were co-transformed with pET-AEQ for expression of aequorin and pRham. Three different versions of pRham were used: the empty vector as control (empty), the vector containing LjMLO4 CDS optimized for expression in E. coli (MLO4, 65 kDa) and a truncated version of the gene (AA 1-265, MLO4Δ, 31 kDa) mimicking the putative truncated protein in mlo4-3 L. japonicus mutant line. A) Schematic representation of the two versions of LjMLO4 expressed in E. coli. The representative image of MLO topology (modified from Kusch et al . 2016 ) highlights the missing domains in LjMLO4Δ. B) Western blot showing the expression of LjMLO4-HIS and LjMLO4Δ-HIS in E. coli cells using <t>anti-HIS</t> antibody. D-G) Ca 2+ influx after injection of 1 mM CaCl 2 represented as Ca 2+ traces along time (D), level of Ca 2+ after 2 minutes (E) and after 3 minutes (F), total Ca 2+ mobilized over time (G). Statistical analysis was conducted via Kruskal-Wallis test followed by Dunn’s post-hoc correction (only p-values < 0.1 are reported).
Mouse Antibodies, supplied by SouthernBiotech, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


E. coli cells were co-transformed with pET-AEQ for expression of aequorin and pRham. Three different versions of pRham were used: the empty vector as control (empty), the vector containing LjMLO4 CDS optimized for expression in E. coli (MLO4, 65 kDa) and a truncated version of the gene (AA 1-265, MLO4Δ, 31 kDa) mimicking the putative truncated protein in mlo4-3 L. japonicus mutant line. A) Schematic representation of the two versions of LjMLO4 expressed in E. coli. The representative image of MLO topology (modified from Kusch et al . 2016 ) highlights the missing domains in LjMLO4Δ. B) Western blot showing the expression of LjMLO4-HIS and LjMLO4Δ-HIS in E. coli cells using anti-HIS antibody. D-G) Ca 2+ influx after injection of 1 mM CaCl 2 represented as Ca 2+ traces along time (D), level of Ca 2+ after 2 minutes (E) and after 3 minutes (F), total Ca 2+ mobilized over time (G). Statistical analysis was conducted via Kruskal-Wallis test followed by Dunn’s post-hoc correction (only p-values < 0.1 are reported).

Journal: bioRxiv

Article Title: A symbiotic MLO gene regulates root development via RALF34-triggered Ca 2+ signalling in Lotus japonicus

doi: 10.1101/2025.09.18.676995

Figure Lengend Snippet: E. coli cells were co-transformed with pET-AEQ for expression of aequorin and pRham. Three different versions of pRham were used: the empty vector as control (empty), the vector containing LjMLO4 CDS optimized for expression in E. coli (MLO4, 65 kDa) and a truncated version of the gene (AA 1-265, MLO4Δ, 31 kDa) mimicking the putative truncated protein in mlo4-3 L. japonicus mutant line. A) Schematic representation of the two versions of LjMLO4 expressed in E. coli. The representative image of MLO topology (modified from Kusch et al . 2016 ) highlights the missing domains in LjMLO4Δ. B) Western blot showing the expression of LjMLO4-HIS and LjMLO4Δ-HIS in E. coli cells using anti-HIS antibody. D-G) Ca 2+ influx after injection of 1 mM CaCl 2 represented as Ca 2+ traces along time (D), level of Ca 2+ after 2 minutes (E) and after 3 minutes (F), total Ca 2+ mobilized over time (G). Statistical analysis was conducted via Kruskal-Wallis test followed by Dunn’s post-hoc correction (only p-values < 0.1 are reported).

Article Snippet: 6xHis-tagged proteins were detected by overnight incubation at 4 °C with HRP-conjugated mouse Anti-His-Tag antibody (SB194b; SouthernBiotech, Birmingham, USA), 1:20000 dilution in 5% milk T-TBS.

Techniques: Transformation Assay, Expressing, Plasmid Preparation, Control, Mutagenesis, Modification, Western Blot, Injection