Antibodies

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Human Lambda Light Chain (free and bound) goat polyclonal antibody, FITC

Applications ELISA, ID, IF, IHC, IP
Reactivities Human
Conjugation FITC

Human Lambda Light Chain (free and bound) goat polyclonal antibody, TRITC

Applications ELISA, ID, IF, IHC, IP
Reactivities Human
Conjugation TRITC

Mouse lambda light chain (free and bound) goat polyclonal antibody, Serum

Applications ELISA, IF, IHC, IP, WB
Reactivities Mouse
Conjugation Unconjugated

Mouse IgM (Fc specific) goat polyclonal antibody, Azide Free

Applications Can be used as unlabelled primary or secondary reagent for indirect detection of IgM at the cellular and subcellular level by staining of appropriately treated cell and tissue substrates; to prepare conjugates of the user’s own choice; to prepare an insoluble immunoaffinity adsorbent or a solid phase antibody reagent by coupling to an artificial carrier and as catching antibody in non-isotopic methodology and solid phase immunochemistry.
When applied in any cytochemical or histochemical staining procedure or solid phase coupling technique, the optimum concentration of the IgG preparation should be established by titration before being used.
Typical working dilutions:
In histochemistry are usually between 1/50 and 1/250.
In ELISA and comparable non-precipitating antibody-binding assays between 1/500 and 1/5000.
Reactivities Mouse
Conjugation Unconjugated

Alb goat polyclonal antibody, Azide Free

Applications ELISA, ID, IF, IP, WB
Reactivities Rat
Conjugation Unconjugated

Alb goat polyclonal antibody, FITC

Applications ELISA, IF, IHC, IP, R
Reactivities Rat
Conjugation FITC

6xHistidine Epitope Tag (HHHHHH) chicken polyclonal antibody, Purified

Applications IP, WB
Conjugation Unconjugated

Mouse IgM (Fc specific) rabbit polyclonal antibody, Azide Free

Applications Can be used: 
As unlabelled primary or secondary antibody reagent for indirect detection of IgM in Mouse cells, tissues and body fluids in Immunofluorescence and Immunoenzyme assay methods.
For the production of immunoconjugates with a selected marker.
To prepare immunoaffinity adsorbents by coupling to an artificial carrier.
In non-isotopic methodology based on solid phase immunochemistry (e.g. ELISA), both as catching antibody and detection reagent.
In Western blotting.
When applied in any immunocytochemical or histochemical staining procedure or solid phase coupling techniques, the optimum concentration of this product should be established before.
Recommneded Working Dilutions:
Histochemistry: 1/100-1/250.
ELISA and comparable non-precipitating antibody-binding assays: 1/1000-1/5000. 
Precipitin titre: not less than 1/64 when tested against normal Mouse serum in agar-block immunodiffusion titration. 

Performance testing: Titre, specificity and reactivity of the subclass specific cross-adsorbed IgG is further evaluated in a number of highly sensitive non-precipitating antibody-binding assay systems. These performance tests include direct single and double identification of cIg in mouse cell and tissue substrates and their evaluation as second antibody in the analysis of human cells and tissues after reacting with a primary monoclonal mouse antibody to a human antigen. The quantitative specific recognition ability is verified in double staining procedures together with reference reagents of known specificity and reactivity.
Reactivities Mouse
Conjugation Unconjugated

Mouse IgM (Fc specific) rabbit polyclonal antibody, FITC

Applications ELISA.
Immunocytochemistry.
Immunohistochemistry on Frozen Sections.
(In)direct immunofluorescence.
In direct staining of cytoplasmic IgM in fixed mouse cells and tissue substrates; to identify circulating IgM antibodies in serodiagnostic microbiology and autoimmune diseases; to identify a specific antigen or immune complex using a reference antibody of mouse in the middle layer of the test procedure. 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 Dilutions1/20- 1/80.
Reactivities Mouse
Conjugation FITC

Mouse IgM (Fc specific) rabbit polyclonal antibody, TRITC

Applications ELISA. 
Immunocytochemistry.  
(In)direct immunofluorescence

Immunohistochemistry on Frozen Sections. 
Direct immunofluorescence staining of cytoplasmic Ig of appropriately treated cell and tissue substrates; to demonstrate immunoglobulins or specific antibodies in cells and tissues; to identify circulating antibodies in serodiagnostic microbiology and autoimmune diseases. 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: 1/10- 1/80.
Reactivities Mouse
Conjugation TRITC

c Fos (FOS) rabbit polyclonal antibody, Purified

Applications ELISA, IHC, IP, WB
Reactivities Human
Conjugation Unconjugated

CACNA1C pSer1928 rabbit polyclonal antibody, Serum

Applications ELISA, IP, WB
Reactivities Human
Conjugation Unconjugated

Herpes Virus Type 6 / HHV6 Early Antigen mouse monoclonal antibody, clone 600, Purified

Applications ELISA, IF, IHC, IP, WB
Reactivities Human Herpesvirus 6
Conjugation Unconjugated

Hepatitis B Core Antigen / HBcAg (ayw) mouse monoclonal antibody, clone 10E11, Ascites

Applications ELISA, IHC, IP, WB
Reactivities Hepatitis B Virus
Conjugation Unconjugated

NUP153 mouse monoclonal antibody, clone nup7A8, Supernatant

Applications IF, IHC, IP, WB
Reactivities Amphibian, Human, Mouse, Rat, Xenopus
Conjugation Unconjugated