biotinylated universal secondary antibody (Vector Laboratories)


Name:
Biotinylated Universal Antibody Horse Anti Mouse Rabbit IgG
Description:
Biotinylated Universal Antibody Horse Anti Mouse Rabbit IgG is prepared using proprietary immunization schedules that produce high affinity antibodies The antibodies are then purified by affinity chromatography and cross reactivities that are likely to interfere with specific labeling are removed by solid phase adsorption techniques The biotinylated secondary antibodies are conjugated to ensure the maximum degree of labeling without compromising the specificity or affinity of the antibody These antibodies are subjected to rigorous quality control assays and can be used for tissue and cell staining ELISAs and blots Biotinylated Universal Horse Anti Mouse Rabbit IgG H L is supplied in liquid format With some exceptions the recommended dilution for most applications is 1 50 H L indicates the antibody recognizes both heavy and light chains This biotinylated Universal secondary antibody is produced in horse and binds equally well to both mouse IgG H L and rabbit IgG H L primary antibodies The high staining quality and sensitivity achieved using this product is equivalent to that obtained with either our biotinylated anti mouse IgG H L or biotinylated anti rabbit IgG H L used individually The convenience of using a single biotinylated secondary antibody for both species of primary and the elimination of possible mistakes in using the wrong secondary antibody is an advantage of this product Note This antibody has significant crossreactivity for rodent IgG and is not recommended for use in staining rodent tissue
Catalog Number:
ba-1400
Price:
None
Category:
Antibodies
Reactivity:
Universal Mouse Rabbit
Size:
2 1 mg
Host:
Horse
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Structured Review

Biotinylated Universal Antibody Horse Anti Mouse Rabbit IgG is prepared using proprietary immunization schedules that produce high affinity antibodies The antibodies are then purified by affinity chromatography and cross reactivities that are likely to interfere with specific labeling are removed by solid phase adsorption techniques The biotinylated secondary antibodies are conjugated to ensure the maximum degree of labeling without compromising the specificity or affinity of the antibody These antibodies are subjected to rigorous quality control assays and can be used for tissue and cell staining ELISAs and blots Biotinylated Universal Horse Anti Mouse Rabbit IgG H L is supplied in liquid format With some exceptions the recommended dilution for most applications is 1 50 H L indicates the antibody recognizes both heavy and light chains This biotinylated Universal secondary antibody is produced in horse and binds equally well to both mouse IgG H L and rabbit IgG H L primary antibodies The high staining quality and sensitivity achieved using this product is equivalent to that obtained with either our biotinylated anti mouse IgG H L or biotinylated anti rabbit IgG H L used individually The convenience of using a single biotinylated secondary antibody for both species of primary and the elimination of possible mistakes in using the wrong secondary antibody is an advantage of this product Note This antibody has significant crossreactivity for rodent IgG and is not recommended for use in staining rodent tissue
https://www.bioz.com/result/biotinylated universal secondary antibody/product/Vector Laboratories
Average 97 stars, based on 1 article reviews
Price from $9.99 to $1999.99
Images
1) Product Images from "Fermentation of Green Tea with 2% Aquilariae lignum Increases the Anti-Diabetic Activity of Green Tea Aqueous Extracts in the High Fat-Fed Mouse"
Article Title: Fermentation of Green Tea with 2% Aquilariae lignum Increases the Anti-Diabetic Activity of Green Tea Aqueous Extracts in the High Fat-Fed Mouse
Journal: Nutrients
doi: 10.3390/nu7115447

Figure Legend Snippet: Representative histological images of the insulin- and glucagon-immunoreactive cells in the pancreas, taken from NFD or HFD supplied mice. ( A ) Intact control: Normal pellet diet supplied vehicle control mice; 10 mL/kg of distilled water oral administered mice; ( B ) HFD (vehicle) control: 10 mL/kg of distilled water oral administered mice with HFD supply; ( C ) Simvastatin: 10 mg/kg of simvastatin oral administered mice with HFD supply; ( D ) Metformin: 250 mg/kg of metformin oral administered mice with HFD supply; ( E ) GT400: 400 mg/kg of GT oral administered mice with HFD supply; ( F ) fGT400: 400 mg/kg of fGT oral administered mice with HFD supply; ( G ) fGT200: 200 mg/kg of fGT oral administered mice with HFD supply; ( H ) fGT100: 100 mg/kg of fGT oral administered mice with HFD supply. NFD, normal fat pellet diet; HFD, high fat diet; GT, green tea extracts; fGT, Aquilariae lignum -fermented green tea extracts. All immunostained by avidin-biotin-peroxidase complex. Scale bars = 80 µm.
Techniques Used: Mouse Assay, Avidin-Biotin Assay
2) Product Images from "Beneficial effects of dried pomegranate juice concentrated powder on ultraviolet B-induced skin photoaging in hairless mice"
Article Title: Beneficial effects of dried pomegranate juice concentrated powder on ultraviolet B-induced skin photoaging in hairless mice
Journal: Experimental and Therapeutic Medicine
doi: 10.3892/etm.2017.4626

Figure Legend Snippet: Representative immunohistochemistrical images of dorsal back skin tissues, taken from unexposed intact or UVB-exposed hairless mice. (A) Intact vehicle control; (B) UVB control; (C) UVB-exposed mice treated with 2 ml/kg PCS mice; (D) UVB-exposed mice treated with 100 mg/kg PCP; (E) UVB-exposed mice treated with 200 mg/kg PCP; (F) UVB-exposed mice treated with 400 mg/kg PCP. All avidin-biotin complex immunostaining. Scale bars=50 µm. UVB, ultraviolet B; 4-HNE, 4-hydroxynonenal; PARP, cleaved poly(ADP-ribose) polymerase; MMP-9, matrix metalloproteinase 9; PCP, dried pomegranate juice concentrated powder; PCS, pomegranate juice concentrated solution.
Techniques Used: Mouse Assay, Avidin-Biotin Assay, Immunostaining
3) Product Images from "Bathing Effects of Various Seawaters on Allergic (Atopic) Dermatitis-Like Skin Lesions Induced by 2,4-Dinitrochlorobenzene in Hairless Mice"
Article Title: Bathing Effects of Various Seawaters on Allergic (Atopic) Dermatitis-Like Skin Lesions Induced by 2,4-Dinitrochlorobenzene in Hairless Mice
Journal: Evidence-based Complementary and Alternative Medicine : eCAM
doi: 10.1155/2015/179185

Figure Legend Snippet: Representative immunohistochemical images of IFN- γ , iNOS, IL-1 β , IL-2, and TNF- α in the submandibular LN tissues, taken from unexposed intact or DNCB-induced AD mice bathing on seawaters or topical application of DEXA. Noticeable increases of the numbers of IFN- γ , iNOS, IL-1 β , IL-2, and TNF- α immunolabeled cells were observed in DNCB control mice as compared with intact vehicle control hairless mice, respectively. However, these submandibular LN hypersensitivities related increases of cytokine immunoreactive cells were significantly inhibited by topical treatment of 1% DEXA, bathing on the ESGW, WSGW, ESSW, and WSSW as compared with DNCB control mice, in that order, respectively. AD = allergic/atopic-like dermatitis; DNCB = 2,4-dinitrochlorobenzene; DEXA = dexamethasone-water soluble; WSSW = west surface seawater collected around Wepo-ri (Ganghwa-do, Republic of Korea); WSGW = west saline groundwater collected at Yonggungoncheon (Seokmo-do, Republic of Korea); ESSW = east surface seawater collected around Nagok-ri (Uljin, Republic of Korea); ESGW = east saline groundwater collected around Hoojeong-ri (Uljin, Republic of Korea); LN = lymph node; IFN = interferon; IL = interleukin; iNOS = inducible nitric oxide synthase (2); TNF = tumor necrosis factor; ABC = avidin-biotin complex. All being ABC immunostain. Scale bars = 40 μ m.
Techniques Used: Immunohistochemistry, Mouse Assay, Immunolabeling, Avidin-Biotin Assay

Figure Legend Snippet: Representative immunohistochemical images of IFN- γ , iNOS, IL-1 β , IL-2, and TNF- α in the splenic tissues, taken from unexposed intact or DNCB-induced AD mice bathing on seawaters or topical application of DEXA. Dramatic and noticeable increases of the numbers of IFN- γ , iNOS, IL-1 β , IL-2, and TNF- α immunolabeled cells were observed in DNCB control mice as compared with intact vehicle control hairless mice, respectively. However, these hypersensitivities related increases of cytokine immunoreactive cells were significantly inhibited by topical treatment of 1% DEXA and bathing on the ESGW, WSGW, ESSW, and WSSW as compared with DNCB control mice, in that order, respectively. (a) Intact vehicle control mice bathing on the distilled water; (b) DNCB control mice bathing on the distilled water; (c) AD mice bathing on the WSSW; (d) AD mice bathing on the WSGW; (e) AD mice bathing on the ESSW; (f) AD mice bathing on the ESGW; (g) 1% DEXA topically applied AD mice. AD = allergic/atopic-like dermatitis; DNCB = 2,4-dinitrochlorobenzene; DEXA = dexamethasone-water soluble; WSSW = west surface seawater collected around Wepo-ri (Ganghwa-do, Republic of Korea); WSGW = west saline groundwater collected at Yonggungoncheon (Seokmo-do, Republic of Korea); ESSW = east surface seawater collected around Nagok-ri (Uljin, Republic of Korea); ESGW = east saline groundwater collected around Hoojeong-ri (Uljin, Republic of Korea); IFN = interferon; IL = interleukin; iNOS = inducible nitric oxide synthase (2); TNF = tumor necrosis factor; ABC = avidin-biotin complex. All being ABC immunostain. Scale bars = 40 μ m.
Techniques Used: Immunohistochemistry, Mouse Assay, Immunolabeling, Avidin-Biotin Assay

Figure Legend Snippet: Representative immunohistochemical images of dermal IFN- γ , iNOS, IL-1 β , IL-2, and TNF- α in the dorsal back skin tissues, taken from unexposed intact or DNCB-induced AD mice bathing on seawaters or topical application of DEXA. Dramatic infiltrations of dermal IFN- γ , iNOS, IL-1 β , IL-2, and TNF- α immunolabeled cells were observed in DNCB control mice as compared with intact vehicle control hairless mice, respectively. However, these increases of immunoreactivities of IFN- γ , iNOS, IL-1 β , IL-2, and TNF- α in the dermis were significantly inhibited by bathing on the ESGW, WSGW, ESSW, and WSSW as compared with DNCB control mice, in that order, respectively. Topical application of 1% DEXA also significantly reduced the increases of dermal IFN- γ , iNOS, IL-1 β , IL-2, and TNF- α immunolabeled cells induced by NDCB treatment as compared with DNCB control mice, in this experiment. (a) Intact vehicle control mice bathing on the distilled water; (b) DNCB control mice bathing on the distilled water; (c) AD mice bathing on the WSSW; (d) AD mice bathing on the WSGW; (e) AD mice bathing on the ESSW; (f) AD mice bathing on the ESGW; (g) 1% DEXA topically applied AD mice. AD = allergic/atopic-like dermatitis; DNCB = 2,4-dinitrochlorobenzene; DEXA = dexamethasone-water soluble; WSSW = west surface seawater collected around Wepo-ri (Ganghwa-do, Republic of Korea); WSGW = west saline groundwater collected at Yonggungoncheon (Seokmo-do, Republic of Korea); ESSW = east surface seawater collected around Nagok-ri (Uljin, Republic of Korea); ESGW = east saline groundwater collected around Hoojeong-ri (Uljin, Republic of Korea); IFN = interferon; IL = interleukin; iNOS = inducible nitric oxide synthase (2); TNF = tumor necrosis factor; ABC = avidin-biotin complex. All being ABC immunostain. Scale bars = 40 μ m.
Techniques Used: Immunohistochemistry, Mouse Assay, Immunolabeling, Avidin-Biotin Assay

Figure Legend Snippet: Representative immunohistochemical images of caspase-3, PARP, NT, 4-HNE, and MMP-9 in the dorsal back skin tissues, taken from unexposed intact or DNCB-induced AD mice bathing on seawaters or topical application of DEXA. Noticeable elevations of caspase-3, PARP, NT, and 4-HNE immunoreactive epidermal cells, dermal MMP-9 immunoreactivities were detected on the dorsal back skin tissues in DNCB control mice, respectively. However, these increases of immunoreactivities related AD signs were significantly inhibited by bathing on the ESGW, WSGW, ESSW, and WSSW as compared with DNCB control mice, in that order, respectively. Topical application of 1% DEXA also significantly reduced the increases of caspase-3, PARP, NT, and 4-HNE immunoreactive epidermal cells and dermal MMP-9 immunoreactivities as compared with DNCB control mice, in this experiment. (a) Intact vehicle control mice bathing on the distilled water; (b) DNCB control mice bathing on the distilled water; (c) AD mice bathing on the WSSW; (d) AD mice bathing on the WSGW; (e) AD mice bathing on the ESSW; (f) AD mice bathing on the ESGW; (g) 1% DEXA topically applied AD mice. AD = allergic/atopic-like dermatitis; DNCB = 2,4-dinitrochlorobenzene; DEXA = dexamethasone-water soluble; WSSW = west surface seawater collected around Wepo-ri (Ganghwa-do, Republic of Korea); WSGW = west saline groundwater collected at Yonggungoncheon (Seokmo-do, Republic of Korea); ESSW = east surface seawater collected around Nagok-ri (Uljin, Republic of Korea); ESGW = east saline groundwater collected around Hoojeong-ri (Uljin, Republic of Korea); PARP = cleaved poly (ADP-ribose) polymerase; NT = nitrotyrosine; 4-HNE = 4-hydroxynonenal; MMP = matrix metalloprotease; ABC = avidin-biotin complex. All being ABC immunostain. Scale bars = 40 μ m.
Techniques Used: Immunohistochemistry, Mouse Assay, Avidin-Biotin Assay
4) Product Images from "Anti-Diabetic Obesity Effects of Wasabia Japonica Matsum Leaf Extract on 45% Kcal High-Fat Diet-Fed Mice"
Article Title: Anti-Diabetic Obesity Effects of Wasabia Japonica Matsum Leaf Extract on 45% Kcal High-Fat Diet-Fed Mice
Journal: Nutrients
doi: 10.3390/nu12092837

Figure Legend Snippet: Representative histological images of the insulin- and glucagon-immunoreactive cells in the pancreas, taken from NFD or HFD supplied mice. ( a ) Vehicle (distilled water) 10 mL/kg orally administered mice with NFD supply (Intact control); ( b ) Vehicle 10 mL/kg orally administered mice with HFD supply (HFD control); ( c ) 250 mg/kg of metformin oral administered mice with HFD supply (Metformin); ( d ) WL 200 mg/kg orally administered mice with HFD supply (WL200); ( e ) WL 100 mg/kg orally administered mice with HFD supply (WL100); ( f ) WL 50 mg/kg orally administered mice with HFD supply (WL50). NFD = Normal pellet diet; HFD = 45% Kcal high-fat diet; WL = Wasabi Leaf/Folium, Wasabia japonica (Miq.) Matsum extracts; IS = Pancreatic islet. All immunostained by avidin-biotin-peroxidase complex. Scale bars = 80 µm.
Techniques Used: Mouse Assay, Avidin-Biotin Assay
5) Product Images from "Fermentation with Aquilariae Lignum Enhances the Anti-Diabetic Activity of Green Tea in Type II Diabetic db/db Mouse"
Article Title: Fermentation with Aquilariae Lignum Enhances the Anti-Diabetic Activity of Green Tea in Type II Diabetic db/db Mouse
Journal: Nutrients
doi: 10.3390/nu6093536

Figure Legend Snippet: Representative histological images of the insulin-immunoreactive cells in the pancreas, taken from intact normoglycemic or db/db mice. ( A ) Intact control mouse; ( B ) db control mouse; ( C ) metformin 250 mg/kg treated db mouse; ( D ) GT 400 mg/kg treated db mouse; ( E ) fGT 400 mg/kg treated db mouse; ( F ) fGT 200 mg/kg treated db mouse; ( G ) fGT 100 mg/kg treated db mouse. GT, Green tea aqueous lyophilized extracts; fGT, Aquilariae Lignum-fermented green tea aqueous lyophilized extracts; IS, pancreatic islet; PD, pancreatic secretory duct. All immunostained by avidin-biotin-peroxidase complex. Scale bars = 80 µm.
Techniques Used: Mouse Assay, Avidin-Biotin Assay

Figure Legend Snippet: Representative histological images of the glucagon-immunoreactive cells in the pancreas, taken from intact normoglycemic or db/db mice. ( A ) Intact control mouse; ( B ) db control mouse; ( C ) metformin 250 mg/kg treated db mouse; ( D ) GT 400 mg/kg treated db mouse; ( E ) fGT 400 mg/kg treated db mouse; ( F ) fGT 200 mg/kg treated db mouse; ( G ) fGT 100 mg/kg treated db mouse. GT, Green tea aqueous lyophilized extracts; fGT, Aquilariae Lignum-fermented green tea aqueous lyophilized extracts; IS, pancreatic islet; PD, pancreatic secretory duct. All immunostained by avidin-biotin-peroxidase complex. Scale bars = 80 µm.
Techniques Used: Mouse Assay, Avidin-Biotin Assay
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