ArtNr |
709-006-149 |
Hersteller |
Jackson ImmunoResearch
|
Menge |
0,5 mg |
Kategorie |
|
Typ |
Antibody Polyclonal |
Format |
Liquid |
Specific against |
Human (Homo sapiens) |
Host |
Donkey |
Konjugat/Tag |
Unconjugated |
Purity |
The antibody was purified from antisera by a combination of pepsin digestion and immunoaffinity chromatography using antigens coupled to agarose beads. Fc fragments and whole IgG molecules have been removed. |
ECLASS 10.1 |
32160702 |
ECLASS 11.0 |
32160702 |
UNSPSC |
12352203 |
Lieferbar |
|
Specificity |
IgG (H+L) |
Manufacturer - Category |
F(ab')₂ Fragment Affinity-Purified Antibodies |
Storage Conditions |
Store at 2-8°C under sterile conditions. Prepare working dilution on day of use. |
Expiration Date |
one year from date of receipt. The expiration date may be extended if test results are acceptable for the intended use. |
Preservative |
None |
Suggested Working Concentration or Dilution Range |
10-20 µg / ml
Dilution factors are presented in the form of a range because the optimal dilution is a function of many factors, such as antigen density, permeability, etc. The actual dilution used must be determined empirically. |
Buffer |
0.01M Sodium Phosphate, 0.25M NaCl, pH 7.6 |
Manufacturer - Specificity |
IgG (H+L) |
Clonality |
Polyclonal |
Minimal Cross Reactivity |
Bovine, Chicken, Goat, Guinea Pig, Syrian Hamster, Horse, Mouse, Rabbit, Rat, Sheep Serum Proteins |
Infomation |
Based on immunoelectrophoresis and/or ELISA, the antibody reacts with whole molecule human IgG. It also reacts with the light chains of other human 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, chicken, goat, guinea pig, syrian hamster, horse, mouse, rabbit, rat and sheep serum proteins, but it may cross-react with immunoglobulins from other species. |
Physical State |
Sterile-filtered liquid |
Purity |
The antibody was purified from antisera by a combination of pepsin digestion and immunoaffinity chromatography using antigens coupled to agarose beads. Fc fragments and whole IgG molecules have been removed. |
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