anti no 1 Search Results


anti-acneic cream no 2  (SEPPIC Inc)
90
SEPPIC Inc anti-acneic cream no 2
Anti Acneic Cream No 2, supplied by SEPPIC Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti-acneic cream no 2/product/SEPPIC Inc
Average 90 stars, based on 1 article reviews
anti-acneic cream no 2 - by Bioz Stars, 2026-03
90/100 stars
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polyclonal rabbit anti-mouse daf antibody (antibody no. 1, used at 1:2000; see below)  (Becton Dickinson)
90
Becton Dickinson polyclonal rabbit anti-mouse daf antibody (antibody no. 1, used at 1:2000; see below)
Northern blot (A–C) and Western blot (D–F) analysis showing differential expression of <t>DAF</t> and Crry in the mouse skin and kidney (kid, Ki). In A–C, RNA samples from WT (w) or DAFKO (k) MRL/lpr mice were separated and the blot was hybridized with either a GPI-DAF cDNA probe (which recognizes both GPI-DAF and TM-DAF cDNAs) (A), or a TM-DAF-specific cDNA probe (B), or a Crry cDNA probe (C). RNAs from the mouse lung and testis (tes) were used as positive controls. Two GPI-DAF mRNA species, with variable relative abundance in different tissues, are known to be transcribed. 18,19 The position of the 18S ribosomal RNA was indicated by a horizontal bar in A–C. In D–F, total proteins from the WT (w, WT) or DAFKO (k, KO) MRL/lpr mouse lung (Lu), skin (Sk), or kidney (kid, Ki), as well as proteins from vector-transfected (−) or mouse DAF cDNA-transfected (+) HEK cells, were separated on 8% sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblotted with anti-mouse DAF <t>polyclonal</t> antibody no. 1 (D) or antibody no. 2 (E) or a monoclonal antibody against mouse Crry (F). DAF protein expressed in HEK cells (lane marked with + in D) migrated as a broad 66-kd band, reflecting its glycoprotein nature. 1,46 The signal in the vector-transfected HEK cells (lane marked with − in D) may represent human DAF endogenous to HEK cells. Note the apparent difference between WT and KO mice in lung and skin, but not kidney DAF signals (D, E). Immunofluorescence analysis of skin (with anti-DAF polyclonal antibody no. 1) showed DAF to be primarily expressed in the elastic fibers (bright green, arrows in G). No specific staining was detected in the DAFKO mouse skin (H). Orange color in G and H represents counterstain with propidium iodide.
Polyclonal Rabbit Anti Mouse Daf Antibody (Antibody No. 1, Used At 1:2000; See Below), supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/polyclonal rabbit anti-mouse daf antibody (antibody no. 1, used at 1:2000; see below)/product/Becton Dickinson
Average 90 stars, based on 1 article reviews
polyclonal rabbit anti-mouse daf antibody (antibody no. 1, used at 1:2000; see below) - by Bioz Stars, 2026-03
90/100 stars
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primary antibody rabbit anti-human cb 1 igg no. 1  (Alpha Diagnostics)
90
Alpha Diagnostics primary antibody rabbit anti-human cb 1 igg no. 1
Northern blot (A–C) and Western blot (D–F) analysis showing differential expression of <t>DAF</t> and Crry in the mouse skin and kidney (kid, Ki). In A–C, RNA samples from WT (w) or DAFKO (k) MRL/lpr mice were separated and the blot was hybridized with either a GPI-DAF cDNA probe (which recognizes both GPI-DAF and TM-DAF cDNAs) (A), or a TM-DAF-specific cDNA probe (B), or a Crry cDNA probe (C). RNAs from the mouse lung and testis (tes) were used as positive controls. Two GPI-DAF mRNA species, with variable relative abundance in different tissues, are known to be transcribed. 18,19 The position of the 18S ribosomal RNA was indicated by a horizontal bar in A–C. In D–F, total proteins from the WT (w, WT) or DAFKO (k, KO) MRL/lpr mouse lung (Lu), skin (Sk), or kidney (kid, Ki), as well as proteins from vector-transfected (−) or mouse DAF cDNA-transfected (+) HEK cells, were separated on 8% sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblotted with anti-mouse DAF <t>polyclonal</t> antibody no. 1 (D) or antibody no. 2 (E) or a monoclonal antibody against mouse Crry (F). DAF protein expressed in HEK cells (lane marked with + in D) migrated as a broad 66-kd band, reflecting its glycoprotein nature. 1,46 The signal in the vector-transfected HEK cells (lane marked with − in D) may represent human DAF endogenous to HEK cells. Note the apparent difference between WT and KO mice in lung and skin, but not kidney DAF signals (D, E). Immunofluorescence analysis of skin (with anti-DAF polyclonal antibody no. 1) showed DAF to be primarily expressed in the elastic fibers (bright green, arrows in G). No specific staining was detected in the DAFKO mouse skin (H). Orange color in G and H represents counterstain with propidium iodide.
Primary Antibody Rabbit Anti Human Cb 1 Igg No. 1, supplied by Alpha Diagnostics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/primary antibody rabbit anti-human cb 1 igg no. 1/product/Alpha Diagnostics
Average 90 stars, based on 1 article reviews
primary antibody rabbit anti-human cb 1 igg no. 1 - by Bioz Stars, 2026-03
90/100 stars
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anti-digoxigenin-ap fab fragments no: 1 093 274  (Boehringer Mannheim)
90
Boehringer Mannheim anti-digoxigenin-ap fab fragments no: 1 093 274
Northern blot (A–C) and Western blot (D–F) analysis showing differential expression of <t>DAF</t> and Crry in the mouse skin and kidney (kid, Ki). In A–C, RNA samples from WT (w) or DAFKO (k) MRL/lpr mice were separated and the blot was hybridized with either a GPI-DAF cDNA probe (which recognizes both GPI-DAF and TM-DAF cDNAs) (A), or a TM-DAF-specific cDNA probe (B), or a Crry cDNA probe (C). RNAs from the mouse lung and testis (tes) were used as positive controls. Two GPI-DAF mRNA species, with variable relative abundance in different tissues, are known to be transcribed. 18,19 The position of the 18S ribosomal RNA was indicated by a horizontal bar in A–C. In D–F, total proteins from the WT (w, WT) or DAFKO (k, KO) MRL/lpr mouse lung (Lu), skin (Sk), or kidney (kid, Ki), as well as proteins from vector-transfected (−) or mouse DAF cDNA-transfected (+) HEK cells, were separated on 8% sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblotted with anti-mouse DAF <t>polyclonal</t> antibody no. 1 (D) or antibody no. 2 (E) or a monoclonal antibody against mouse Crry (F). DAF protein expressed in HEK cells (lane marked with + in D) migrated as a broad 66-kd band, reflecting its glycoprotein nature. 1,46 The signal in the vector-transfected HEK cells (lane marked with − in D) may represent human DAF endogenous to HEK cells. Note the apparent difference between WT and KO mice in lung and skin, but not kidney DAF signals (D, E). Immunofluorescence analysis of skin (with anti-DAF polyclonal antibody no. 1) showed DAF to be primarily expressed in the elastic fibers (bright green, arrows in G). No specific staining was detected in the DAFKO mouse skin (H). Orange color in G and H represents counterstain with propidium iodide.
Anti Digoxigenin Ap Fab Fragments No: 1 093 274, supplied by Boehringer Mannheim, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti-digoxigenin-ap fab fragments no: 1 093 274/product/Boehringer Mannheim
Average 90 stars, based on 1 article reviews
anti-digoxigenin-ap fab fragments no: 1 093 274 - by Bioz Stars, 2026-03
90/100 stars
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elisa-anti-q kit no. 1  (Pasteur Institute)
90
Pasteur Institute elisa-anti-q kit no. 1
Northern blot (A–C) and Western blot (D–F) analysis showing differential expression of <t>DAF</t> and Crry in the mouse skin and kidney (kid, Ki). In A–C, RNA samples from WT (w) or DAFKO (k) MRL/lpr mice were separated and the blot was hybridized with either a GPI-DAF cDNA probe (which recognizes both GPI-DAF and TM-DAF cDNAs) (A), or a TM-DAF-specific cDNA probe (B), or a Crry cDNA probe (C). RNAs from the mouse lung and testis (tes) were used as positive controls. Two GPI-DAF mRNA species, with variable relative abundance in different tissues, are known to be transcribed. 18,19 The position of the 18S ribosomal RNA was indicated by a horizontal bar in A–C. In D–F, total proteins from the WT (w, WT) or DAFKO (k, KO) MRL/lpr mouse lung (Lu), skin (Sk), or kidney (kid, Ki), as well as proteins from vector-transfected (−) or mouse DAF cDNA-transfected (+) HEK cells, were separated on 8% sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblotted with anti-mouse DAF <t>polyclonal</t> antibody no. 1 (D) or antibody no. 2 (E) or a monoclonal antibody against mouse Crry (F). DAF protein expressed in HEK cells (lane marked with + in D) migrated as a broad 66-kd band, reflecting its glycoprotein nature. 1,46 The signal in the vector-transfected HEK cells (lane marked with − in D) may represent human DAF endogenous to HEK cells. Note the apparent difference between WT and KO mice in lung and skin, but not kidney DAF signals (D, E). Immunofluorescence analysis of skin (with anti-DAF polyclonal antibody no. 1) showed DAF to be primarily expressed in the elastic fibers (bright green, arrows in G). No specific staining was detected in the DAFKO mouse skin (H). Orange color in G and H represents counterstain with propidium iodide.
Elisa Anti Q Kit No. 1, supplied by Pasteur Institute, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/elisa-anti-q kit no. 1/product/Pasteur Institute
Average 90 stars, based on 1 article reviews
elisa-anti-q kit no. 1 - by Bioz Stars, 2026-03
90/100 stars
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self-made gynecological anti-inflammatory no.1 decoction  (CH Instruments)
90
CH Instruments self-made gynecological anti-inflammatory no.1 decoction
The RCTs of effective CHM formula for PID with oral administration.
Self Made Gynecological Anti Inflammatory No.1 Decoction, supplied by CH Instruments, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/self-made gynecological anti-inflammatory no.1 decoction/product/CH Instruments
Average 90 stars, based on 1 article reviews
self-made gynecological anti-inflammatory no.1 decoction - by Bioz Stars, 2026-03
90/100 stars
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mouse anti-cytokeratin no. 1-8  (Boehringer Mannheim)
90
Boehringer Mannheim mouse anti-cytokeratin no. 1-8
The RCTs of effective CHM formula for PID with oral administration.
Mouse Anti Cytokeratin No. 1 8, supplied by Boehringer Mannheim, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mouse anti-cytokeratin no. 1-8/product/Boehringer Mannheim
Average 90 stars, based on 1 article reviews
mouse anti-cytokeratin no. 1-8 - by Bioz Stars, 2026-03
90/100 stars
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Image Search Results


Northern blot (A–C) and Western blot (D–F) analysis showing differential expression of DAF and Crry in the mouse skin and kidney (kid, Ki). In A–C, RNA samples from WT (w) or DAFKO (k) MRL/lpr mice were separated and the blot was hybridized with either a GPI-DAF cDNA probe (which recognizes both GPI-DAF and TM-DAF cDNAs) (A), or a TM-DAF-specific cDNA probe (B), or a Crry cDNA probe (C). RNAs from the mouse lung and testis (tes) were used as positive controls. Two GPI-DAF mRNA species, with variable relative abundance in different tissues, are known to be transcribed. 18,19 The position of the 18S ribosomal RNA was indicated by a horizontal bar in A–C. In D–F, total proteins from the WT (w, WT) or DAFKO (k, KO) MRL/lpr mouse lung (Lu), skin (Sk), or kidney (kid, Ki), as well as proteins from vector-transfected (−) or mouse DAF cDNA-transfected (+) HEK cells, were separated on 8% sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblotted with anti-mouse DAF polyclonal antibody no. 1 (D) or antibody no. 2 (E) or a monoclonal antibody against mouse Crry (F). DAF protein expressed in HEK cells (lane marked with + in D) migrated as a broad 66-kd band, reflecting its glycoprotein nature. 1,46 The signal in the vector-transfected HEK cells (lane marked with − in D) may represent human DAF endogenous to HEK cells. Note the apparent difference between WT and KO mice in lung and skin, but not kidney DAF signals (D, E). Immunofluorescence analysis of skin (with anti-DAF polyclonal antibody no. 1) showed DAF to be primarily expressed in the elastic fibers (bright green, arrows in G). No specific staining was detected in the DAFKO mouse skin (H). Orange color in G and H represents counterstain with propidium iodide.

Journal:

Article Title: Deletion of Decay-Accelerating Factor (CD55) Exacerbates Autoimmune Disease Development in MRL/lpr Mice

doi:

Figure Lengend Snippet: Northern blot (A–C) and Western blot (D–F) analysis showing differential expression of DAF and Crry in the mouse skin and kidney (kid, Ki). In A–C, RNA samples from WT (w) or DAFKO (k) MRL/lpr mice were separated and the blot was hybridized with either a GPI-DAF cDNA probe (which recognizes both GPI-DAF and TM-DAF cDNAs) (A), or a TM-DAF-specific cDNA probe (B), or a Crry cDNA probe (C). RNAs from the mouse lung and testis (tes) were used as positive controls. Two GPI-DAF mRNA species, with variable relative abundance in different tissues, are known to be transcribed. 18,19 The position of the 18S ribosomal RNA was indicated by a horizontal bar in A–C. In D–F, total proteins from the WT (w, WT) or DAFKO (k, KO) MRL/lpr mouse lung (Lu), skin (Sk), or kidney (kid, Ki), as well as proteins from vector-transfected (−) or mouse DAF cDNA-transfected (+) HEK cells, were separated on 8% sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblotted with anti-mouse DAF polyclonal antibody no. 1 (D) or antibody no. 2 (E) or a monoclonal antibody against mouse Crry (F). DAF protein expressed in HEK cells (lane marked with + in D) migrated as a broad 66-kd band, reflecting its glycoprotein nature. 1,46 The signal in the vector-transfected HEK cells (lane marked with − in D) may represent human DAF endogenous to HEK cells. Note the apparent difference between WT and KO mice in lung and skin, but not kidney DAF signals (D, E). Immunofluorescence analysis of skin (with anti-DAF polyclonal antibody no. 1) showed DAF to be primarily expressed in the elastic fibers (bright green, arrows in G). No specific staining was detected in the DAFKO mouse skin (H). Orange color in G and H represents counterstain with propidium iodide.

Article Snippet: Staining of DAF in the skin was performed by using a polyclonal rabbit anti-mouse DAF antibody (antibody no. 1, used at 1:2000; see below), 30 followed by a fluorescein isothiocyanate-conjugated rat anti-rabbit IgG (1:200, PharMingen).

Techniques: Northern Blot, Western Blot, Expressing, Plasmid Preparation, Transfection, Polyacrylamide Gel Electrophoresis, Immunofluorescence, Staining

The RCTs of effective CHM formula for PID with oral administration.

Journal: Evidence-based Complementary and Alternative Medicine : eCAM

Article Title: Evidence for the Use of Complementary and Alternative Medicine for Pelvic Inflammatory Disease: A Literature Review

doi: 10.1155/2022/1364297

Figure Lengend Snippet: The RCTs of effective CHM formula for PID with oral administration.

Article Snippet: [ ] , RCT , 90 , Control arm: levofloxacin + ornidazole Treatment arm: self-made Gynecological Anti-Inflammatory No. 1 Decoction on the basis of the control arm , Control arm: TFR, 75.56% ∗ (34 of 45) Treatment arm: TFR, 93.33% (42 of 45) , Self-made Gynecological Anti-Inflammatory No.1 Decoction: Delavay honeysuckle (Jin yin hua), dandelion (Pu gong ying), weeping forsythia capsule (Lian qiao), Oldenlandia (Bai hua she she cao), Herba Patriniae (Bai jiang cao), heartleaf houttuynia (Yu xing cao), Sargent gloryvine stem (Da xue teng), red peony (Chi shao), Moutan (Mu dan pi), cinnamon bark (Rou gui), green tangerine peer (Qing pi), Morinda root (Ba ji tian), white Atractylodes rhizome (Bai zhu), citrus (Chen pi), Coix seed (Yi yi ren), Poria (Fu ling) , Not mentioned drop-out rate and small sample size.

Techniques: Control, Capsules

The RCTs of effective CHMRE for PID.

Journal: Evidence-based Complementary and Alternative Medicine : eCAM

Article Title: Evidence for the Use of Complementary and Alternative Medicine for Pelvic Inflammatory Disease: A Literature Review

doi: 10.1155/2022/1364297

Figure Lengend Snippet: The RCTs of effective CHMRE for PID.

Article Snippet: [ ] , RCT , 90 , Control arm: levofloxacin + ornidazole Treatment arm: self-made Gynecological Anti-Inflammatory No. 1 Decoction on the basis of the control arm , Control arm: TFR, 75.56% ∗ (34 of 45) Treatment arm: TFR, 93.33% (42 of 45) , Self-made Gynecological Anti-Inflammatory No.1 Decoction: Delavay honeysuckle (Jin yin hua), dandelion (Pu gong ying), weeping forsythia capsule (Lian qiao), Oldenlandia (Bai hua she she cao), Herba Patriniae (Bai jiang cao), heartleaf houttuynia (Yu xing cao), Sargent gloryvine stem (Da xue teng), red peony (Chi shao), Moutan (Mu dan pi), cinnamon bark (Rou gui), green tangerine peer (Qing pi), Morinda root (Ba ji tian), white Atractylodes rhizome (Bai zhu), citrus (Chen pi), Coix seed (Yi yi ren), Poria (Fu ling) , Not mentioned drop-out rate and small sample size.

Techniques: Control, Staining, Infection