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Key Documents

11426346910

Roche

Anti-Fluorescein-POD, Fab fragments

from sheep

Synonyme(s) :

antibody

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About This Item

Code UNSPSC :
12352203

Source biologique

sheep

Niveau de qualité

Conjugué

peroxidase conjugate

Forme d'anticorps

purified immunoglobulin

Type de produit anticorps

primary antibodies

Clone

polyclonal

Forme

lyophilized (stabilized)

Conditionnement

pkg of 150 U

Fabricant/nom de marque

Roche

Température de stockage

2-8°C

Description générale

Fab fragments from polyclonal anti-fluorescein antibodies, conjugated to horseradish peroxidase. The reagent is an anti-fluorescein antibody, Fab fragments from sheep, conjugated with horse-radishperoxidase (POD). After immunization with fluorescein the sheep IgG (immunoglobulin G) was purified by ion exchange chromatography and the specific IgG was isolated by immunosorption. The Fab fragments obtained by papain digestion were purified by gel filtration, conjugated with POD and stabilized in 60mM Tris-Hepes-buffer, 0.4% bovine immunoglobulin (w/v), 0.2% Germall II (w/v), pH 7.2.

Spécificité

The polyclonal antibody reacts with free and bound fluorescein.

Application

Anti-Fluorescein-POD, Fab fragments are used for detection of fluorescein-labeled compounds in:
  • Dot blot
  • ELISA (enzyme-linked immunosorbent assay)
  • Immunohistocytochemistry
  • In situ hybridization
  • Southern blot
  • Western blot

Notes préparatoires

Working concentration: Working concentration of conjugate depends on application and substrate. The following concentrations should be taken as a guideline:
  • Dot blot: 150 mU/ml
  • ELISA: 50 to 150 mU/ml
  • Immunohistocytochemistry: 250 to 500 mU/ml
  • In situ hybridization: 1.5 to 7.5 U/ml
  • Southern blot: 150 mU/ml
  • Western blot: 500 to 1000 mU/ml

Working solution: 100 mM Tris-HCl, 150 mM NaCl, pH 7.5. If necessary 1% Blocking reagent (w/v), dry milk powder, 1 to 5% heat inactivated fetal calf serum (v/v) or sheep normal serum can be used for reduction of unspecific binding.

Reconstitution

Add 1 ml double-distilled water to a final concentration of 150 U/ml.

Autres remarques

For life science research only. Not for use in diagnostic procedures.

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Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Skin Sens. 1

Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

does not flash

Point d'éclair (°C)

does not flash


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Nicolle A Bonar et al.
Development (Cambridge, England), 144(5), 784-794 (2017-01-28)
Animals capable of adult regeneration require specific signaling to control injury-induced cell proliferation, specification and patterning, but comparatively little is known about how the regeneration blastema assembles differentiating cells into well-structured functional tissues. Using the planarian Schmidtea mediterranea as a
Chen Wang et al.
Cell discovery, 2, 16029-16029 (2016-08-24)
Pigmentation processes occur from invertebrates to mammals. Owing to the complexity of the pigmentary system, in vivo animal models for pigmentation study are limited. Planarians are capable of regenerating any missing part including the dark-brown pigments, providing a promising model
Kunio Kondoh et al.
Nature, 532(7597), 103-106 (2016-03-24)
Instinctive reactions to danger are critical to the perpetuation of species and are observed throughout the animal kingdom. The scent of predators induces an instinctive fear response in mice that includes behavioural changes, as well as a surge in blood
Jingwen Liu et al.
PLoS biology, 17(8), e3000203-e3000203 (2019-08-21)
Zebrafish dorsal forerunner cells (DFCs) undergo vigorous proliferation during epiboly and then exit the cell cycle to generate Kupffer's vesicle (KV), a ciliated organ necessary for establishing left-right (L-R) asymmetry. DFC proliferation defects are often accompanied by impaired cilia elongation
Elena Grassi et al.
Frontiers in cellular neuroscience, 12, 518-518 (2019-01-29)
Alternative polyadenylation (APA) is a widespread mechanism involving about half of the expressed genes, resulting in varying lengths of the 3' untranslated region (3'UTR). Variations in length and sequence of the 3'UTR may underlie changes of post-transcriptional processing, localization, miRNA

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