購入して、WBでの検出を試みましたが、目的のバンドは検出できませんでした。WBには不向きのようです。
SAB4503523
Anti-UBE3B antibody produced in rabbit
Anti-UBE3B antibody produced in rabbit
1 of 1 reviewers received a sample product or took part in a promotion
affinity isolated antibody
Synonym(s):
UBE3B, Ubiquitin-protein ligase E3B
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100 μG
$522.00
$522.00
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100 μG
$522.00
About This Item
UNSPSC Code:
12352203
NACRES:
NA.41
$522.00
Usually ships in 5 business days. (Orders outside of US, please allow an additional 1-2 weeks for delivery)
Notify Me
Get notified when this item is ready to ship via email.
biological source
rabbit
conjugate
unconjugated
antibody form
affinity isolated antibody
antibody product type
primary antibodies
clone
polyclonal
form
buffered aqueous solution
mol wt
antigen 123 kDa
species reactivity
human
concentration
~1 mg/mL
technique(s)
ELISA: 1:10000
western blot: 1:500-1:1000
NCBI accession no.
UniProt accession no.
shipped in
wet ice
storage temp.
−20°C
target post-translational modification
unmodified
Gene Information
human ... UBE3B(89910)
General description
Anti-UBE3B Antibody detects endogenous levels of total UBE3B protein.
Immunogen
The antiserum was produced against synthesized peptide derived from human UBE3B.
Immunogen Range: 581-630
Immunogen Range: 581-630
Features and Benefits
Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.
Physical form
Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
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
10 - Combustible liquids
wgk_germany
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
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Andrea Braganza et al.
The Journal of biological chemistry, 292(6), 2470-2484 (2016-12-23)
Recent genome-wide studies found that patients with hypotonia, developmental delay, intellectual disability, congenital anomalies, characteristic facial dysmorphic features, and low cholesterol levels suffer from Kaufman oculocerebrofacial syndrome (KOS, also reported as blepharophimosis-ptosis-intellectual disability syndrome). The primary cause of KOS is
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