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Merck

11093274910

Roche

Anty-Digoxigenin-AP, fragmenty Fab

from sheep

Synonim(y):

antydigoksygenina, digoksygenina

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About This Item

Kod UNSPSC:
12352203

pochodzenie biologiczne

sheep

Poziom jakości

białko sprzężone

alkaline phosphatase conjugate

forma przeciwciała

purified immunoglobulin

rodzaj przeciwciała

primary antibodies

klon

polyclonal

Formularz

solution

opakowanie

pkg of 200 μL (150 U)

producent / nazwa handlowa

Roche

izotyp

IgG

temp. przechowywania

2-8°C

Opis ogólny

Digoxigenin is a hapten, useful in labeling and detection of nucleic acids. This product contains Fab fragments from polyclonal anti-digoxigenin antibodies, conjugated to alkaline phosphatase. Anti-Digoxigenin-AP, Fab fragments are useful for the detection of digoxigenin-labeled compounds.

Specyficzność

The polyclonal antibody from sheep is specific to digoxigenin and digoxin and shows no cross-reactivity with other steroids, such as human estrogens and androgens.
Heat inactivation: yes

Zastosowanie

Use Anti-Digoxigenin-AP, Fab fragments for the detection of digoxigenin-labeled compounds using:
  • cDNA array
  • Colony/plaque hybridization
  • Dot blot
  • ELISA
  • Gel shift assay
  • Immunohistocytochemistry
  • In situ hybridization
  • Nonradioactive DNA sequencing blot
  • Northern blot
  • RNase protection assay
  • Southern blot
  • Western blot
  • Fluorescent in situ hybridization
  • Section in situ hybridization and whole mount in situ hybridization
  • Electrophoretic mobility shift assay

Uwaga dotycząca przygotowania

After immunization with digoxigenin, sheep IgG 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 to the specific label, and stabilized in buffer.
Working concentration: Working concentration of conjugate will depend on the application and substrate. The following concentrations should be taken as a guideline:
  • Dot blot: 150 mU/ml
  • ELISA: 150 to 300 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: 250 to 500 mU/ml

Working solution: Northern blot, Southern blot
100 mM Maleic acid, 150 mM NaCl, pH 7.5.
Western blot
50 mM Tris-HCl, 150 mM NaCl, pH 7.5
other applications
100 mM Tris-HCl, 150 mM NaCl, pH 7.5

1% Blocking reagent (w/v), 1 to 5% heat inactivated fetal calf serum (v/v) or sheep normal serum can be used for reduction of unspecific binding.
Storage conditions (working solution): Diluted conjugate is stable at 2 to 8 °C for 12 hours.
Always prepare freshly!

Komentarz do analizy

  • Cross reactivity to digitoxin and digitoxigenin: <1 %
  • No cross reactivity with other human estrogen or androgen steroids, e.g. estradiol or testosterone
  • Cross reactivity with digoxin: not known
  • Conjugate does not bind to itself at all
  • Normally one molecule of the conjugate binds to one molecule digoxigenin, although ther are two possible binding sites for digoxigenin
  • Nonspecific binding to RNA is not expected

Inne uwagi

For life science research only. Not for use in diagnostic procedures.
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Klasa zagrożenia wodnego (WGK)

WGK 1

Temperatura zapłonu (°F)

No data available

Temperatura zapłonu (°C)

No data available


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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Bruce A Molitoris et al.
Journal of the American Society of Nephrology : JASN, 20(8), 1754-1764 (2009-05-28)
Proximal tubule cells (PTCs), which are the primary site of kidney injury associated with ischemia or nephrotoxicity, are the site of oligonucleotide reabsorption within the kidney. We exploited this property to test the efficacy of siRNA targeted to p53, a
Bree Rumballe et al.
CSH protocols, 2008, pdb-pdb (2008-01-01)
INTRODUCTIONSection in situ hybridization (SISH) is a high-resolution tool used to analyze gene expression patterns. This protocol utilizes the Tecan Freedom EVO150 platform to perform high-throughput SISH on paraffin sections to detect mRNA with a digoxigenin (DIG)-labeled probe. The slide
Use of In Situ Hybridization to Examine Gene Expression in the Embryonic, Neonatal, and Adult Urogenital System.
Rumballe B A, et al.
Kidney Development: Methods and Protocols, 223-239 (2012)
Exorhodopsin and melanopsin systems in the pineal complex and brain at early developmental stages of Atlantic halibut (Hippoglossus hippoglossus).
Eilertsen M, et al.
The Journal of Comparative Neurology, 522(18), 4003-4022 (2014)
Tara C Carlisle et al.
The Journal of comparative neurology, 522(4), 861-875 (2013-08-14)
Electrical synapses are expressed prominently in the developing and mature nervous systems. Unlike chemical synapses, little is known about the developmental role of electrical synapses, reflecting the limitations imposed by the lack of selective pharmacological blockers. At a molecular level

Produkty

Digoxigenin (DIG) labeling methods and kits for DNA and RNA DIG probes, random primed DNA labeling, nick translation labeling, 5’ and 3’ oligonucleotide end-labeling.

Metody znakowania digoksygeniną (DIG) i zestawy do sond DNA i RNA DIG, znakowanie DNA z losowym primerem, znakowanie nickiem translacyjnym, znakowanie końcowe oligonukleotydów 5' i 3'.

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