12-506
Goat Anti-Mouse IgG (H+L) Antibody, FITC conjugate
Upstate®, from goat
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.42
Recommended Products
biological source
goat
Quality Level
conjugate
FITC conjugate
antibody form
affinity purified immunoglobulin
antibody product type
secondary antibodies
clone
polyclonal
species reactivity
mouse
manufacturer/tradename
Upstate®
technique(s)
flow cytometry: suitable
immunocytochemistry: suitable
immunofluorescence: suitable
immunohistochemistry: suitable
shipped in
dry ice
target post-translational modification
unmodified
Related Categories
Specificity
Recognizes mouse IgG, both heavy and light chains. Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-fluorescein, anti-goat serum, mouse IgG and mouse serum.
Immunogen
Mouse IgG whole molecule.
Application
Absorption Wavelength: 495nm
Emission Wavelength: 528nm
Fluorochrome/Protein Molar Ratio: 3.2
Suitable for immunomicroscopy and flow cytometry or FACS analysis, as well as other antibody based fluorescent assays requiring lot-to-lot consistency. Optimal antibody dilution should be determined by the researcher.
Emission Wavelength: 528nm
Fluorochrome/Protein Molar Ratio: 3.2
Suitable for immunomicroscopy and flow cytometry or FACS analysis, as well as other antibody based fluorescent assays requiring lot-to-lot consistency. Optimal antibody dilution should be determined by the researcher.
Detect Mouse IgG (H+L) using this Goat anti-Mouse IgG (H+L) Antibody, FITC conjugate validated for use in FC, IF, IC, IH.
Research Category
Secondary & Control Antibodies
Secondary & Control Antibodies
Research Sub Category
Whole Immunoglobulin Secondary Antibodies
Whole Immunoglobulin Secondary Antibodies
Quality
Routinely evaluated by immunomicroscopy, flow cytometry or FACS analysis, as well as other antibody based fluorescent assays requiring lot-to-lot consistency.
Physical form
ImmunoAffinity Purified
Lyophilized powder; lyophilized from 500 μl of 20 mM potassium phosphatase, pH 7.2, 150 mM NaCl, 0.10% sodium azide and 10 mg/ml BSA.
Storage and Stability
Stable for 1 year at -20°C from date of shipment. Once opened, dilute with 250μl of distilled water, aliquot, and freeze at -20°C or below for extended storage. Avoid multiple freeze-thaw cycles. Dilute only immediately prior to use.
Legal Information
UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
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.
Not finding the right product?
Try our Product Selector Tool.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2
Storage Class Code
6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Effect of tacrolimus on chemokine production by corneal myofibroblasts via toll-like receptors, compared with cyclosporine and dexamethasone.
Nobuyuki Ebihara,Kaori Ohtomo,Tomoko Tokura,Hiroko Ushio,Akira Murakami
Cornea null
Differential regulation of lipogenesis and leptin production by independent signaling pathways and rosiglitazone during human adipocyte differentiation.
Nayan G Patel,Julie C Holder,Stephen A Smith,Sudesh Kumar,Margaret C Eggo
Diabetes null
Rapamycin inhibits human adipocyte differentiation in primary culture.
A Bell,L Grunder,A Sorisky
Obesity Research null
R E Payne et al.
British journal of cancer, 106(11), 1790-1797 (2012-04-28)
Current approaches for detecting circulating tumour cells (CTCs) in blood are dependent on CTC enrichment and are based either on surface epithelial markers on CTCs or on cell size differences. The objectives of this study were to develop and characterise
Nitya N Srivastava et al.
Environmental and molecular mutagenesis, 55(5), 436-448 (2014-02-07)
Radiation exposure is a serious threat to biomolecules, particularly DNA, proteins and lipids. Various exogenous substances have been reported to protect these biomolecules. In this study we explored the effect of pre-treatment with G-002M, a mixture of three active derivatives
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service