Goat F(ab)2 Anti-Human lambda (lambda chain) Antibody - 709-1111, Unconjugated, Polyclonal

Catalog Number: DNA-SEC-183725
Article Name: Goat F(ab)2 Anti-Human lambda (lambda chain) Antibody - 709-1111, Unconjugated, Polyclonal
Biozol Catalog Number: DNA-SEC-183725
Supplier Catalog Number: DNA-SEC-183725
Alternative Catalog Number: DNA-SEC-183725
Manufacturer: dianova
Host: Goat
Category: Antikörper
Application: ELISA,IHC,WB
Species Reactivity: Human
Immunogen: Human lambda light chain
Conjugation: Unconjugated
Alternative Names: Goat F(ab)2 Anti-Human lambda (lambda chain) Antibody, Goat F(ab)2 Anti-Human lambda chain Antibody
Format: F(ab')2
Target Specificity: Lambda (light chain)
Cross-Adsorption (MinX): no cross-adsorbtion
F(ab)2 Antibody was generated by enzymatic cleavage and subsequent separation from the Fc fragment. Because of their smaller size, F(ab)2 fragments offer several advantages over intact antibodies for use in certain immunochemical techniques and experimen
Clonality: Polyclonal
Concentration: 1.0 mg/mL
Isotype: Ig
Buffer: 0.125 M Sodium Borate, 0.075 M Sodium Chloride, 0.005 M EDTA, pH 8.0
Purity: This product was prepared from monospecific antiserum by immunoaffinity chromatography using antigens coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities, pepsin digestion and chromatographic separation. Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Goat Serum, Human IgG and Human Serum. No reaction was observed against anti-Pepsin or anti-Goat IgG F(c). Specificity was confirmed by ELISA at less than 1% cross reactivity against other human heavy or light chain isotypes.
Form: Liquid (sterile filtered)
Formula: 125 mM Sodium Borate,75 mM NaCl,5 mM EDTA,pH 8,0,sterile filtered,0,01% NaN3
Target: Human
Antibody Type: Secondary Antibody
Application Dilute: ELISA Dilution: 1:6,000, Immunohistochemistry Dilution: 1:1,000 - 1:5,000, Western Blot Dilution: 1:1,000 - 1:5,000
Application Notes: Suitable for highly specific immunological methods requiring extremely low background levels, absence of F(c) mediated binding, lot-to-lot consistency, high titer and specificity.