Antibodies

Rabbit Polyclonal Anti-WNT2 Antibody (Internal)

Applications IHC
Reactivities Human (Predicted: Mouse, Rat, Bat, Bovine, Dog, Hamster, Pig, Rabbit, Sheep, Chicken, Guinea Pig)

Rabbit anti-ACAT2 polyclonal antibody

Applications WB
Reactivities Human, Rat, Sheep, Pig, Mouse

Rabbit polyclonal anti CRF (ovine); neat antiserum

Applications ELISA
Reactivities Sheep

GFAP rabbit polyclonal antibody, Purified

Applications IHC
Reactivities Bovine, Chicken, Guinea Pig, Hamster, Human, Monkey, Mouse, Rat, Sheep

Rabbit Polyclonal Prion protein Antibody

Applications WB
Reactivities Bovine, Sheep

Rabbit Polyclonal Prion protein Antibody

Applications WB
Reactivities Bovine, Sheep, Avian

Rabbit Polyclonal Prion protein Antibody

Applications WB
Reactivities Bovine, Sheep

Rabbit polyclonal Hsp110 Antibody

Applications WB
Reactivities Human, Monkey, Hamster, Rat, Mouse, Sheep, Yeast, Cow

Rabbit polyclonal SOD (Mn) Antibody

Applications IHC
Reactivities Human, Rat, Mouse, Bovine, Canine, Chicken, Gerbil, Guinea Pig, Pig, Hamster, Rabbit, Monkey, Sheep, Xenopus

Rabbit Polyclonal Anti-Calnexin -CT Antibody

Applications WB
Reactivities Human, Monkey, Mouse, Rat, Bovine, Dog, Hamster, Rabbit, Pig, Quail, Sheep, Xenopus (weak), Guinea Pig, Drosophila (weak), Chicken (weak)

Goat Anti-C12orf29 (aa30-43) Antibody

Applications WB
Reactivities Human (Expected from sequence similarity: Pig, Sheep, Cow)

PTPH1 (PTPN3) pSer459 rabbit polyclonal antibody, Aff - Purified

Applications WB
Reactivities Bovine, Canine, Human, Mouse, Primate, Sheep

Sheep IgM (H+L chain) rabbit polyclonal antibody, Biotin

Applications ELISA.
Dot blot.
Immunoblotting.
Immunocytochemistry.
Immunohistochemistry Paraffin Sections.

Can be used in immunocytochemical and immunohistochemical staining for the detection of IgM at the cellular and subcellular level by immunofluorescence staining of appropriately treated cell and tissue substrates, and to demonstrate circulating antibodies in serodiagnostic microbiology and autoimmune diseases, where IgM and IgG antibodies can be expected. As a second step an avidin or streptavidin conjugate of the user’s choice has to be used. This immunoconjugate is not pre-diluted. The optimum working dilution of each conjugate should be established by titration before being used. Excess labelled antibody must be avoided because it may cause high unspecific background staining and interfere with the specific signal.
Recommended Working Dilutions:
Histochemistry and Cytochemical Use: 1/100-1/250.
ELISA and comparable non-precipitating antibody-binding assays: 1/1,000-1/8,000.
Reactivities Sheep
Conjugation Biotin

Sheep IgM (H+L chain) rabbit polyclonal antibody, HRP

Applications ELISA.
Dot blot.
Immunoblotting.
Immunocytochemistry.
Immunohistochemistry Paraffin Sections.

Can be used in enzyme-immunocytochemical and immunohistochemical staining for the detection of IgM at the cellular and subcellular level by staining of appropriately treated cell and tissue substrates, and to demonstrate circulating antibodies in serodiagnostic microbiology and autoimmune diseases, where IgM and IgG antibodies can be expected. This immunoconjugate is not pre-diluted. The optimum working dilution of each conjugate should be established by titration before being used. Excess labelled antibody must be avoided because it may cause high unspecific background staining and interfere with the specific signal.
Recommended Working Dilutions:
Histochemistry and Cytochemical Use: 1/100-1/250.
ELISA and comparable non-precipitating antibody-binding assays: 1/2,000-1/10,000.
Reactivities Sheep
Conjugation HRP

Sheep IgG (H+L chain) rabbit polyclonal antibody, HRP

Applications ELISA.
Dot blot.
Immunoblotting.
Immunocytochemistry.
Immunohistochemistry Paraffin Sections.

Can be used in enzyme-immunocytochemical and immunohistochemical staining for the detection of IgG, antigen or antibody, of appropriately treated cell and tissue substrates at the cellular and subcellular level. In non-isotopic assay methodology (e.g. ELISA) to identify and measure a specific IgG in sheep serum or other body fluid. In electron microscopy, since the complex between the conjugated antibody and the antigen also has electron-dense properties. This immunoconjugate is not pre-diluted. The optimum working dilution of each conjugate should be established by titration before being used. Excess labelled antibody must be avoided because it may cause high unspecific background staining and interfere with the specific signal.
Recommended Working Dilutions:
Histochemistry and Cytochemical Use: 1/100-1/500.
ELISA and comparable non-precipitating antibody-binding assays: 1/1,000-1/10.000.
Reactivities Sheep
Conjugation HRP