Alexa Fluor® 647-conjugated AffiniPure Fab Fragment Goat Anti-Guinea Pig IgG, Fc Fragment Specific

Fab fragment antibodies are generated by papain digestion of whole IgG antibodies to remove the entire Fc portion, including the hinge region. These antibodies are monovalent, containing only a single antigen binding site. The molecular weight of Fab fragments is about 50 kDa.-Based on immunoelectrophoresis and/or ELISA, the antibody reacts with the Fc portion of guinea pig IgG heavy chain but not with the Fab portion of guinea pig immunoglobulins. No antibody was detected against non-immunoglobulin serum proteins. The antibody may cross-react with immunoglobulins from other species.

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Alexa Fluor® 680-conjugated -AffiniPure Fab Fragment Goat Anti-Guinea Pig IgG, Fc Fragment Specific

Fab fragment antibodies are generated by papain digestion of whole IgG antibodies to remove the entire Fc portion, including the hinge region. These antibodies are monovalent, containing only a single antigen binding site. The molecular weight of Fab fragments is about 50 kDa.-Based on immunoelectrophoresis and/or ELISA, the antibody reacts with the Fc portion of guinea pig IgG heavy chain but not with the Fab portion of guinea pig immunoglobulins. No antibody was detected against non-immunoglobulin serum proteins. The antibody may cross-react with immunoglobulins from other species.

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Alexa Fluor® 790-conjugated AffiniPure Fab Fragment Goat Anti-Guinea Pig IgG, Fc Fragment Specific

Fab fragment antibodies are generated by papain digestion of whole IgG antibodies to remove the entire Fc portion, including the hinge region. These antibodies are monovalent, containing only a single antigen binding site. The molecular weight of Fab fragments is about 50 kDa.-Based on immunoelectrophoresis and/or ELISA, the antibody reacts with the Fc portion of guinea pig IgG heavy chain but not with the Fab portion of guinea pig immunoglobulins. No antibody was detected against non-immunoglobulin serum proteins. The antibody may cross-react with immunoglobulins from other species.

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AffiniPure Goat Anti-Syrian Hamster IgG (H+L) (min X Bov,Hrs,Hu,Ms,Rb,Rat Sr Prot)

Whole IgG antibodies are isolated as intact molecules from antisera by immunoaffinity chromatography. They have an Fc portion and two antigen binding Fab portions joined together by disulfide bonds and therefore they are divalent. The average molecular weight is reported to be about 160 kDa. The whole IgG form of antibodies is suitable for the majority of immunodetection procedures and is the most cost effective.-Based on immunoelectrophoresis and/or ELISA, the antibody reacts with whole molecule syrian hamster IgG. It also reacts with the light chains of other syrian hamster immunoglobulins. No antibody was detected against non-immunoglobulin serum proteins. The antibody has been tested by ELISA and/or solid-phase adsorbed to ensure minimal cross-reaction with bovine, horse, human, mouse, rabbit and rat serum proteins, but it may cross-react with immunoglobulins from other species.

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AffiniPure F(ab’)2 Fragment Goat Anti-Syrian Hamster IgG (H+L) (min X Bov,Hrs,Hu,Ms,Rb,Rat Sr Prot)

F(ab’)2 fragment antibodies are generated by pepsin digestion of whole IgG antibodies to remove most of the Fc region while leaving some of the hinge region. F(ab’)2 fragments have two antigen-binding Fab portions linked together by disulfide bonds and therefore they are divalent. The average molecular weight is about 110 kDa. They are used for specific applications, such as to avoid binding of secondary antibodies to live cells with Fc receptors or to Protein A or Protein G.-Based on immunoelectrophoresis and/or ELISA, the antibody reacts with whole molecule syrian hamster IgG. It also reacts with the light chains of other syrian hamster immunoglobulins. No antibody was detected against non-immunoglobulin serum proteins. The antibody has been tested by ELISA and/or solid-phase adsorbed to ensure minimal cross-reaction with bovine, horse, human, mouse, rabbit and rat serum proteins, but it may cross-react with immunoglobulins from other species.

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Rhodamine (TRITC)-conjugated AffiniPure Goat Anti-Syrian Hamster IgG (H+L) (min X Bov,Hrs,Hu,Ms,Rb,Rat Sr Prot)

Whole IgG antibodies are isolated as intact molecules from antisera by immunoaffinity chromatography. They have an Fc portion and two antigen binding Fab portions joined together by disulfide bonds and therefore they are divalent. The average molecular weight is reported to be about 160 kDa. The whole IgG form of antibodies is suitable for the majority of immunodetection procedures and is the most cost effective.-Based on immunoelectrophoresis and/or ELISA, the antibody reacts with whole molecule syrian hamster IgG. It also reacts with the light chains of other syrian hamster immunoglobulins. No antibody was detected against non-immunoglobulin serum proteins. The antibody has been tested by ELISA and/or solid-phase adsorbed to ensure minimal cross-reaction with bovine, horse, human, mouse, rabbit and rat serum proteins, but it may cross-react with immunoglobulins from other species.

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Rhodamine (TRITC) AffiniPure™ F(ab’)₂ Fragment Goat Anti-Syrian Hamster IgG (H+L) (min X Bov, Hrs, Hu, Ms, Rb, Rat Sr Prot)

F(ab’)2 fragment antibodies are generated by pepsin digestion of whole IgG antibodies to remove most of the Fc region while leaving some of the hinge region. F(ab’)2 fragments have two antigen-binding Fab portions linked together by disulfide bonds and therefore they are divalent. The average molecular weight is about 110 kDa. They are used for specific applications, such as to avoid binding of secondary antibodies to live cells with Fc receptors or to Protein A or Protein G.-Based on immunoelectrophoresis and/or ELISA, the antibody reacts with whole molecule syrian hamster IgG. It also reacts with the light chains of other syrian hamster immunoglobulins. No antibody was detected against non-immunoglobulin serum proteins. The antibody has been tested by ELISA and/or solid-phase adsorbed to ensure minimal cross-reaction with bovine, horse, human, mouse, rabbit and rat serum proteins, but it may cross-react with immunoglobulins from other species.

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Peroxidase-conjugated AffiniPure Goat Anti-Syrian Hamster IgG (H+L) (min X Bov Hrs,Hu,Ms,Rb,Rat Sr Prot)

Whole IgG antibodies are isolated as intact molecules from antisera by immunoaffinity chromatography. They have an Fc portion and two antigen binding Fab portions joined together by disulfide bonds and therefore they are divalent. The average molecular weight is reported to be about 160 kDa. The whole IgG form of antibodies is suitable for the majority of immunodetection procedures and is the most cost effective.-Based on immunoelectrophoresis and/or ELISA, the antibody reacts with whole molecule syrian hamster IgG. It also reacts with the light chains of other syrian hamster immunoglobulins. No antibody was detected against non-immunoglobulin serum proteins. The antibody has been tested by ELISA and/or solid-phase adsorbed to ensure minimal cross-reaction with bovine, horse, human, mouse, rabbit and rat serum proteins, but it may cross-react with immunoglobulins from other species.

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Peroxidase-conjugated AffiniPure F(ab’)2 Fragment Goat Anti-Syrian Hamster IgG (H+L) (min X Bov,Hrs,Hu,Ms,Rb,Rat Sr Prot)

F(ab’)2 fragment antibodies are generated by pepsin digestion of whole IgG antibodies to remove most of the Fc region while leaving some of the hinge region. F(ab’)2 fragments have two antigen-binding Fab portions linked together by disulfide bonds and therefore they are divalent. The average molecular weight is about 110 kDa. They are used for specific applications, such as to avoid binding of secondary antibodies to live cells with Fc receptors or to Protein A or Protein G.-Based on immunoelectrophoresis and/or ELISA, the antibody reacts with whole molecule syrian hamster IgG. It also reacts with the light chains of other syrian hamster immunoglobulins. No antibody was detected against non-immunoglobulin serum proteins. The antibody has been tested by ELISA and/or solid-phase adsorbed to ensure minimal cross-reaction with bovine, horse, human, mouse, rabbit and rat serum proteins, but it may cross-react with immunoglobulins from other species.

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