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Key Documents

AP132C

Sigma-Aldrich

Goat Anti-Rabbit IgG Antibody, Cy3 conjugate

Chemicon®, from goat

Synonyme(s) :

Anti-rabbit IgG, Cy3-conjugated antibody, Goat IgG antibody

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About This Item

Code UNSPSC :
12352203
eCl@ss :
32160702
Nomenclature NACRES :
NA.46

Source biologique

goat

Niveau de qualité

Conjugué

CY3 conjugate

Forme d'anticorps

F(ab′)2 fragment of affinity isolated antibody

Type de produit anticorps

secondary antibodies

Clone

polyclonal

Espèces réactives

rabbit

Fabricant/nom de marque

Chemicon®

Technique(s)

immunofluorescence: suitable

Conditions d'expédition

wet ice

Modification post-traductionnelle de la cible

unmodified

Description générale

Immunoglobulin G (IgG), is one of the most abundant proteins in human serum with normal levels between 8-17 mg/mL in adult blood. IgG is important for our defence against microorganisms and the molecules are produced by B lymphocytes as a part of our adaptive immune response. The IgG molecule has two separate functions; to bind to the pathogen that elicited the response and to recruit other cells and molecules to destroy the antigen. The variability of the IgG pool is generated by somatic recombination and the number of specificities in an individual at a given time point is estimated to be 1011 variants.

Spécificité

Rabbit IgG

FLUOROPHORE/PROTEIN:

A552/A280 = 2.64

WAVELENGTH:

Absorption peak = 550 nm, Emission peak = 570 nm.

Application

Research Category
Secondary & Control Antibodies
Research Sub Category
Whole Immunoglobulin Secondary Antibodies
Suggested dilution for most applications: 1:100-1:800

Optimal working dilutions must be determined by end user.
This Goat anti-Rabbit IgG Antibody, Cy3 conjugate is validated for use in IF for the detection of Rabbit IgG.

Forme physique

Lyophilized. Buffer = 0.01 M Sodium Phosphate, 0.25 M NaCl, pH 7.6 with 15 mg/mL BSA, and 0.1% sodium azide.

RECONSTITUTION:

Reconstitute with 2 mL of sterile distilled water

Stockage et stabilité

Maintain lyophilized product at 2-8°C for up to 12 months. After reconstitution the product is stable for several weeks at 2-8°C as an undiluted liquid. For extended storage after reconstitution, add an equal volume of glycerol to make a final concentration of 50% glycerol followed by storage at -20°C in undiluted aliquots for up to 12 months. Please note the concentration of protein (and buffer salts) will decrease to one-half of the original after the addition of glycerol. Avoid repeated freeze/thaw cycles.

Informations légales

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Clause de non-responsabilité

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Mentions de danger

Conseils de prudence

Classification des risques

Aquatic Chronic 3

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3


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Consulter la Bibliothèque de documents

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Cell communication and signaling : CCS, 15(1), 32-32 (2017-09-17)
Antimicrobial peptides are important components of the host defence with a broad range of functions including direct antimicrobial activity and modulation of inflammation. Lack of cathelin-related antimicrobial peptide (CRAMP) was associated with higher mortality and bacterial burden and impaired neutrophil
Mario Gössl et al.
Basic research in cardiology, 104(6), 695-706 (2009-05-22)
Vasa vasorum (VV) neovascularization is a key feature of early atherosclerosis and adds substantial endothelial exchange-surface to the coronary vessel wall. Thus, it is conceivable that VV neovascularization favors the entry of pro-inflammatory and pro-atherosclerotic blood components into the coronary
Sandra Jansen et al.
Infection and immunity, 81(5), 1788-1797 (2013-03-13)
The expression and function of psoriasin in the brain have been insufficiently characterized. Here, we show the induction of psoriasin expression in the central nervous system (CNS) after bacterial and viral stimulation. We used a pneumococcal meningitis in vivo model
Kang Cheng et al.
Stem cell research & therapy, 1(1), 6-6 (2010-05-28)
The ability to expand organ-specific stem/progenitor cells is critical for translational applications, although uncertainties often arise in identifying the lineage of expanded cells. Therefore, superior insights into lineage maintenance mechanisms will be helpful for cell/gene therapy. We studied epithelial cells

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