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antibodies against p2x1  (Santa Cruz Biotechnology)

 
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    Santa Cruz Biotechnology antibodies against p2x1
    Antibodies Against P2x1, supplied by Santa Cruz Biotechnology, 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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    Average 93 stars, based on 1 article reviews
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    antibodies against p2x1 - by Bioz Stars, 2024-10
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    ( a,b ) Influence of CA 2 -2 (0.02 μM) or ATP (30 μM) on duration and ( c,d ) amplitude of Ca 2+ response in murine peritoneal macrophages, loaded with Ca 2+ -sensitive fluorescent probe Fura-2/AM. Arrows show the moment of addition of inductors to macrophages. ( e ) Pre-incubation with different calcium channel blockers and apyrase followed by Ca +2 influx at application of CA 2 -2: 1 control; 2 suramin, 100 μM; 3 PPADS, 10 μM; 4 PhR 10 μM; 5 Phph, 10 μM; 6 BBG 100 μM; 7 KN-62, 10 μM; apyrase, 2.0 U. ( f ) Effect of 30 min pre-incubation with receptor antibodies (ab81122, rabbit polyclonal to <t>P2X1,</t> Abcam,10 μg/mL, orb100036, rabbit polyclonal to P2X4, Biorbyt, 10 μg/mL) and normal rabbit immunoglobulin G (IgG, 10 μg/mL) on Са 2+ influx into peritoneal macrophages (mice, Balb/с line), caused by CA 2 -2 (100 nM); cells alone were used as a control. ( g ) Effect of transient knockdown approach, using P2X4 small interfering RNA, confirms a significant role for the P2X4 receptor in conferring CA 2 -2 induced Ca 2+ entry. ( h ) Expression of P2X4 mRNA in mouse macrophages and reduction of P2X4 mRNA in macrophages by P2X4 siRNA treatment in comparison with macrophages treated with scrambled RNA (PCR data). In addition, control reactions for loading were performed for each sample using β-actin specific primers generating the expected product. DNA molecular weight markers (M) are indicated in base pairs (bp). ( i ) chemical structure of CA 2 -2. All data are presented as m ± sd, *p < 0.05.
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    ( a,b ) Influence of CA 2 -2 (0.02 μM) or ATP (30 μM) on duration and ( c,d ) amplitude of Ca 2+ response in murine peritoneal macrophages, loaded with Ca 2+ -sensitive fluorescent probe Fura-2/AM. Arrows show the moment of addition of inductors to macrophages. ( e ) Pre-incubation with different calcium channel blockers and apyrase followed by Ca +2 influx at application of CA 2 -2: 1 control; 2 suramin, 100 μM; 3 PPADS, 10 μM; 4 PhR 10 μM; 5 Phph, 10 μM; 6 BBG 100 μM; 7 KN-62, 10 μM; apyrase, 2.0 U. ( f ) Effect of 30 min pre-incubation with receptor antibodies (ab81122, rabbit polyclonal to <t>P2X1,</t> Abcam,10 μg/mL, orb100036, rabbit polyclonal to P2X4, Biorbyt, 10 μg/mL) and normal rabbit immunoglobulin G (IgG, 10 μg/mL) on Са 2+ influx into peritoneal macrophages (mice, Balb/с line), caused by CA 2 -2 (100 nM); cells alone were used as a control. ( g ) Effect of transient knockdown approach, using P2X4 small interfering RNA, confirms a significant role for the P2X4 receptor in conferring CA 2 -2 induced Ca 2+ entry. ( h ) Expression of P2X4 mRNA in mouse macrophages and reduction of P2X4 mRNA in macrophages by P2X4 siRNA treatment in comparison with macrophages treated with scrambled RNA (PCR data). In addition, control reactions for loading were performed for each sample using β-actin specific primers generating the expected product. DNA molecular weight markers (M) are indicated in base pairs (bp). ( i ) chemical structure of CA 2 -2. All data are presented as m ± sd, *p < 0.05.
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    ( a,b ) Influence of CA 2 -2 (0.02 μM) or ATP (30 μM) on duration and ( c,d ) amplitude of Ca 2+ response in murine peritoneal macrophages, loaded with Ca 2+ -sensitive fluorescent probe Fura-2/AM. Arrows show the moment of addition of inductors to macrophages. ( e ) Pre-incubation with different calcium channel blockers and apyrase followed by Ca +2 influx at application of CA 2 -2: 1 control; 2 suramin, 100 μM; 3 PPADS, 10 μM; 4 PhR 10 μM; 5 Phph, 10 μM; 6 BBG 100 μM; 7 KN-62, 10 μM; apyrase, 2.0 U. ( f ) Effect of 30 min pre-incubation with receptor antibodies (ab81122, rabbit polyclonal to <t>P2X1,</t> Abcam,10 μg/mL, orb100036, rabbit polyclonal to P2X4, Biorbyt, 10 μg/mL) and normal rabbit immunoglobulin G (IgG, 10 μg/mL) on Са 2+ influx into peritoneal macrophages (mice, Balb/с line), caused by CA 2 -2 (100 nM); cells alone were used as a control. ( g ) Effect of transient knockdown approach, using P2X4 small interfering RNA, confirms a significant role for the P2X4 receptor in conferring CA 2 -2 induced Ca 2+ entry. ( h ) Expression of P2X4 mRNA in mouse macrophages and reduction of P2X4 mRNA in macrophages by P2X4 siRNA treatment in comparison with macrophages treated with scrambled RNA (PCR data). In addition, control reactions for loading were performed for each sample using β-actin specific primers generating the expected product. DNA molecular weight markers (M) are indicated in base pairs (bp). ( i ) chemical structure of CA 2 -2. All data are presented as m ± sd, *p < 0.05.
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    ( a,b ) Influence of CA 2 -2 (0.02 μM) or ATP (30 μM) on duration and ( c,d ) amplitude of Ca 2+ response in murine peritoneal macrophages, loaded with Ca 2+ -sensitive fluorescent probe Fura-2/AM. Arrows show the moment of addition of inductors to macrophages. ( e ) Pre-incubation with different calcium channel blockers and apyrase followed by Ca +2 influx at application of CA 2 -2: 1 control; 2 suramin, 100 μM; 3 PPADS, 10 μM; 4 PhR 10 μM; 5 Phph, 10 μM; 6 BBG 100 μM; 7 KN-62, 10 μM; apyrase, 2.0 U. ( f ) Effect of 30 min pre-incubation with receptor antibodies (ab81122, rabbit polyclonal to <t>P2X1,</t> Abcam,10 μg/mL, orb100036, rabbit polyclonal to P2X4, Biorbyt, 10 μg/mL) and normal rabbit immunoglobulin G (IgG, 10 μg/mL) on Са 2+ influx into peritoneal macrophages (mice, Balb/с line), caused by CA 2 -2 (100 nM); cells alone were used as a control. ( g ) Effect of transient knockdown approach, using P2X4 small interfering RNA, confirms a significant role for the P2X4 receptor in conferring CA 2 -2 induced Ca 2+ entry. ( h ) Expression of P2X4 mRNA in mouse macrophages and reduction of P2X4 mRNA in macrophages by P2X4 siRNA treatment in comparison with macrophages treated with scrambled RNA (PCR data). In addition, control reactions for loading were performed for each sample using β-actin specific primers generating the expected product. DNA molecular weight markers (M) are indicated in base pairs (bp). ( i ) chemical structure of CA 2 -2. All data are presented as m ± sd, *p < 0.05.
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    ( a,b ) Influence of CA 2 -2 (0.02 μM) or ATP (30 μM) on duration and ( c,d ) amplitude of Ca 2+ response in murine peritoneal macrophages, loaded with Ca 2+ -sensitive fluorescent probe Fura-2/AM. Arrows show the moment of addition of inductors to macrophages. ( e ) Pre-incubation with different calcium channel blockers and apyrase followed by Ca +2 influx at application of CA 2 -2: 1 control; 2 suramin, 100 μM; 3 PPADS, 10 μM; 4 PhR 10 μM; 5 Phph, 10 μM; 6 BBG 100 μM; 7 KN-62, 10 μM; apyrase, 2.0 U. ( f ) Effect of 30 min pre-incubation with receptor antibodies (ab81122, rabbit polyclonal to <t>P2X1,</t> Abcam,10 μg/mL, orb100036, rabbit polyclonal to P2X4, Biorbyt, 10 μg/mL) and normal rabbit immunoglobulin G (IgG, 10 μg/mL) on Са 2+ influx into peritoneal macrophages (mice, Balb/с line), caused by CA 2 -2 (100 nM); cells alone were used as a control. ( g ) Effect of transient knockdown approach, using P2X4 small interfering RNA, confirms a significant role for the P2X4 receptor in conferring CA 2 -2 induced Ca 2+ entry. ( h ) Expression of P2X4 mRNA in mouse macrophages and reduction of P2X4 mRNA in macrophages by P2X4 siRNA treatment in comparison with macrophages treated with scrambled RNA (PCR data). In addition, control reactions for loading were performed for each sample using β-actin specific primers generating the expected product. DNA molecular weight markers (M) are indicated in base pairs (bp). ( i ) chemical structure of CA 2 -2. All data are presented as m ± sd, *p < 0.05.
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    ( a,b ) Influence of CA 2 -2 (0.02 μM) or ATP (30 μM) on duration and ( c,d ) amplitude of Ca 2+ response in murine peritoneal macrophages, loaded with Ca 2+ -sensitive fluorescent probe Fura-2/AM. Arrows show the moment of addition of inductors to macrophages. ( e ) Pre-incubation with different calcium channel blockers and apyrase followed by Ca +2 influx at application of CA 2 -2: 1 control; 2 suramin, 100 μM; 3 PPADS, 10 μM; 4 PhR 10 μM; 5 Phph, 10 μM; 6 BBG 100 μM; 7 KN-62, 10 μM; apyrase, 2.0 U. ( f ) Effect of 30 min pre-incubation with receptor antibodies (ab81122, rabbit polyclonal to <t>P2X1,</t> Abcam,10 μg/mL, orb100036, rabbit polyclonal to P2X4, Biorbyt, 10 μg/mL) and normal rabbit immunoglobulin G (IgG, 10 μg/mL) on Са 2+ influx into peritoneal macrophages (mice, Balb/с line), caused by CA 2 -2 (100 nM); cells alone were used as a control. ( g ) Effect of transient knockdown approach, using P2X4 small interfering RNA, confirms a significant role for the P2X4 receptor in conferring CA 2 -2 induced Ca 2+ entry. ( h ) Expression of P2X4 mRNA in mouse macrophages and reduction of P2X4 mRNA in macrophages by P2X4 siRNA treatment in comparison with macrophages treated with scrambled RNA (PCR data). In addition, control reactions for loading were performed for each sample using β-actin specific primers generating the expected product. DNA molecular weight markers (M) are indicated in base pairs (bp). ( i ) chemical structure of CA 2 -2. All data are presented as m ± sd, *p < 0.05.
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    ( a,b ) Influence of CA 2 -2 (0.02 μM) or ATP (30 μM) on duration and ( c,d ) amplitude of Ca 2+ response in murine peritoneal macrophages, loaded with Ca 2+ -sensitive fluorescent probe Fura-2/AM. Arrows show the moment of addition of inductors to macrophages. ( e ) Pre-incubation with different calcium channel blockers and apyrase followed by Ca +2 influx at application of CA 2 -2: 1 control; 2 suramin, 100 μM; 3 PPADS, 10 μM; 4 PhR 10 μM; 5 Phph, 10 μM; 6 BBG 100 μM; 7 KN-62, 10 μM; apyrase, 2.0 U. ( f ) Effect of 30 min pre-incubation with receptor antibodies (ab81122, rabbit polyclonal to P2X1, Abcam,10 μg/mL, orb100036, rabbit polyclonal to P2X4, Biorbyt, 10 μg/mL) and normal rabbit immunoglobulin G (IgG, 10 μg/mL) on Са 2+ influx into peritoneal macrophages (mice, Balb/с line), caused by CA 2 -2 (100 nM); cells alone were used as a control. ( g ) Effect of transient knockdown approach, using P2X4 small interfering RNA, confirms a significant role for the P2X4 receptor in conferring CA 2 -2 induced Ca 2+ entry. ( h ) Expression of P2X4 mRNA in mouse macrophages and reduction of P2X4 mRNA in macrophages by P2X4 siRNA treatment in comparison with macrophages treated with scrambled RNA (PCR data). In addition, control reactions for loading were performed for each sample using β-actin specific primers generating the expected product. DNA molecular weight markers (M) are indicated in base pairs (bp). ( i ) chemical structure of CA 2 -2. All data are presented as m ± sd, *p < 0.05.

    Journal: Scientific Reports

    Article Title: Glycosides from edible sea cucumbers stimulate macrophages via purinergic receptors

    doi: 10.1038/srep39683

    Figure Lengend Snippet: ( a,b ) Influence of CA 2 -2 (0.02 μM) or ATP (30 μM) on duration and ( c,d ) amplitude of Ca 2+ response in murine peritoneal macrophages, loaded with Ca 2+ -sensitive fluorescent probe Fura-2/AM. Arrows show the moment of addition of inductors to macrophages. ( e ) Pre-incubation with different calcium channel blockers and apyrase followed by Ca +2 influx at application of CA 2 -2: 1 control; 2 suramin, 100 μM; 3 PPADS, 10 μM; 4 PhR 10 μM; 5 Phph, 10 μM; 6 BBG 100 μM; 7 KN-62, 10 μM; apyrase, 2.0 U. ( f ) Effect of 30 min pre-incubation with receptor antibodies (ab81122, rabbit polyclonal to P2X1, Abcam,10 μg/mL, orb100036, rabbit polyclonal to P2X4, Biorbyt, 10 μg/mL) and normal rabbit immunoglobulin G (IgG, 10 μg/mL) on Са 2+ influx into peritoneal macrophages (mice, Balb/с line), caused by CA 2 -2 (100 nM); cells alone were used as a control. ( g ) Effect of transient knockdown approach, using P2X4 small interfering RNA, confirms a significant role for the P2X4 receptor in conferring CA 2 -2 induced Ca 2+ entry. ( h ) Expression of P2X4 mRNA in mouse macrophages and reduction of P2X4 mRNA in macrophages by P2X4 siRNA treatment in comparison with macrophages treated with scrambled RNA (PCR data). In addition, control reactions for loading were performed for each sample using β-actin specific primers generating the expected product. DNA molecular weight markers (M) are indicated in base pairs (bp). ( i ) chemical structure of CA 2 -2. All data are presented as m ± sd, *p < 0.05.

    Article Snippet: The suspension of macrophages was fixed and stained with antibodies against P2X1 and P2X4 receptors as described above, and then analyzed with fluorescent flow cytometer FACScalibur (Becton-Dickinson, USA).

    Techniques: Incubation, Small Interfering RNA, Expressing, Molecular Weight