Anti-BLBP antibody (ab110099)
Key features and details
- Goat polyclonal to BLBP
- Suitable for: IHC-P
- Reacts with: Human
- Isotype: IgG
Overview
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Product name
Anti-BLBP antibody
See all BLBP primary antibodies -
Description
Goat polyclonal to BLBP -
Host species
Goat -
Tested Applications & Species
See all applications and species dataApplication Species IHC-P Human -
Immunogen
Synthetic peptide corresponding to Human BLBP (C terminal) conjugated to Keyhole Limpet Haemocyanin (KLH).
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Positive control
- Human cerebellum, heart or skeletal muscle tissue.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles. -
Storage buffer
pH: 7.30
Preservative: 0.02% Sodium azide
Constituents: Tris buffered saline, 0.5% BSA -
Concentration information loading...
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Purity
Immunogen affinity purified -
Clonality
Polyclonal -
Isotype
IgG -
Research areas
Images
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ab110099 at 2.5µg/ml staining BLBP in formalin-fixed, paraffin-embedded Human cerebellum tissue after heat induced antigen retrieval in pH 6.0 citrate buffer.
After incubation with the primary antibody, the slides were incubated with a biotinylated secondary antibody, followed by alkaline phosphatase-streptavidin and chromogen. -
ab110099 at 2.5µg/ml staining BLBP in formalin-fixed, paraffin-embedded Human heart tissue after heat induced antigen retrieval in pH 6.0 citrate buffer.
After incubation with the primary antibody, the slides were incubated with a biotinylated secondary antibody, followed by alkaline phosphatase-streptavidin and chromogen. -
ab110099 at 2.5µg/ml staining BLBP in formalin-fixed, paraffin-embedded Human skeletal muscle tissue after heat induced antigen retrieval in pH 6.0 citrate buffer.
After incubation with the primary antibody, the slides were incubated with a biotinylated secondary antibody, followed by alkaline phosphatase-streptavidin and chromogen. -
ab110099 staining BLBP in Xenopus laevis gindbrain tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections). Tissue was fixed with Bouin's solution, permeabilized with 0.4% Triton X-100 in 3% normal horse serum and blocked with 3% serum for 2 hours at room temperature; antigen retrieval was by heat mediation in 10mM citrate buffer. Samples were incubated with primary antibody (1/100 in 0.4% Triton X-100 in 3% normal horse serum) for 12 hours at 4°C. An undiluted HRP-conjugated horse anti-goat IgG polyclonal was used as the secondary antibody.