MAB5552
Anti-Pax6 Antibody
ascites fluid, clone AD2.38, Chemicon®
Synonym(s):
Anti-AN, Anti-AN2, Anti-ASGD5, Anti-D11S812E, Anti-FVH1, Anti-MGDA, Anti-WAGR
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About This Item
UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41
Pricing and availability is not currently available.
Recommended Products
biological source
mouse
antibody form
ascites fluid
antibody product type
primary antibodies
clone
AD2.38, monoclonal
species reactivity
rat, chicken, mouse, human
manufacturer/tradename
Chemicon®
technique(s)
immunohistochemistry: suitable (paraffin)
western blot: suitable
isotype
IgG1
NCBI accession no.
UniProt accession no.
shipped in
dry ice
target post-translational modification
unmodified
Gene Information
human ... PAX6(5080)
Specificity
Recognizes Pax6. The antibody recognizes both products of the two major alternatively spliced forms.
Immunogen
Recombinant human Pax6.
Application
Detect Pax6 using this Anti-Pax6 Antibody validated for use in IH(P) & WB.
Research Category
Neuroscience
Neuroscience
Research Sub Category
Developmental Neuroscience
Neuronal & Glial Markers
Developmental Neuroscience
Neuronal & Glial Markers
Western blot. The antibody recognizes the 46 and 48 kDa Pax6 proteins.
Immunohistochemistry on paraffin embedded tissue sections.
Optimal working dilutions must be determined by end user.
Immunohistochemistry on paraffin embedded tissue sections.
Optimal working dilutions must be determined by end user.
Target description
46 & 48 kDa
Physical form
Ascites fluid containing no preservatives.
Unpurified
Storage and Stability
Maintain for 1 year at -20°C from date of shipment. Aliquot to avoid repeated freezing and thawing. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Analysis Note
Control
Embryonic eye tissue
Embryonic eye tissue
Other Notes
Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.
This product can not be purchased for resale.
Legal Information
CHEMICON 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.
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Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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’.
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Wen-Chung Liu et al.
International journal of environmental research and public health, 17(11) (2020-06-05)
Maternal high-fructose diets (HFD) impair the learning and memory capacity of adult female offspring via histone deacetylase 4 (HDAC4). Hippocampal adult neurogenesis is important for supporting the function of existing neural circuits. In this study, we investigated the effects of
Mercedes Mirasierra et al.
Diabetologia, 59(4), 766-775 (2016-01-08)
The stimulation of glucagon secretion in response to decreased glucose levels has been studied extensively. In contrast, little is known about the regulation of glucagon gene expression in response to fluctuations in glucose concentration. Paired box 6 (PAX6) is a
Evgeniya V Pushchina et al.
Neural regeneration research, 8(1), 13-23 (2013-01-05)
We investigated the distribution of gamma aminobutyric acid, tyrosine hydroxylase and nitric oxide-producing elements in a cherry salmon Oncorhynchus masou brain at various stages of postnatal ontogenesis by immunohistochemical staining and histochemical staining. The periventricular region cells exhibited the morphology
Susanna Croci et al.
European journal of human genetics : EJHG, 28(10), 1446-1458 (2020-06-17)
Variations in the Forkhead Box G1 (FOXG1) gene cause FOXG1 syndrome spectrum, including the congenital variant of Rett syndrome, characterized by early onset of regression, Rett-like and jerky movements, and cortical visual impairment. Due to the largely unknown pathophysiological mechanisms
Fabio Michelet et al.
Stem cell research & therapy, 11(1), 47-47 (2020-02-06)
Despite increasing demand, current protocols for human pluripotent stem cell (hPSC)-derived retinal pigment epithelium (RPE) remain time, labor, and cost intensive. Additionally, absence of robust methods for selective RPE purification and removal of non-RPE cell impurities prevents upscaling of clinical
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