AV34891
Anti-ZNF57 antibody produced in rabbit
affinity isolated antibody
Synonym(s):
Anti-ZNF424, Anti-Zinc finger protein 57
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About This Item
NACRES:
NA.41
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
polyclonal
Application:
western blot
Species reactivity:
human
Citations:
1
Technique(s):
western blot: suitable
Uniprot accession no.:
Product Name
Anti-ZNF57 antibody produced in rabbit, affinity isolated antibody
biological source
rabbit
conjugate
unconjugated
antibody form
affinity isolated antibody
antibody product type
primary antibodies
clone
polyclonal
form
buffered aqueous solution
mol wt
64 kDa
species reactivity
human
concentration
0.5 mg - 1 mg/mL
technique(s)
western blot: suitable
NCBI accession no.
UniProt accession no.
shipped in
wet ice
storage temp.
−20°C
Quality Level
Gene Information
human ... ZNF57(126295)
Physical form
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Application
Rabbit Anti-ZNF57 antibody is suitable for western blot applications at a concentration of 1 μg/ml.
Biochem/physiol Actions
ZNF57 belongs to the krueppel C2H2-type zinc-finger protein family. It contains 13 C2H2-type zinc fingers and 1 KRAB domain. ZNF57 may be involved in transcriptional regulation.
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.
General description
ZNF57 codes for a zinc finger protein. Genetic variations in ZNF57 may be a potential cause for Mendelian diseases such as hereditary deafness.
Rabbit Anti-ZNF57 antibody recognizes human ZNF57.
Rabbit Anti-ZNF57 antibody recognizes human ZNF57.
Immunogen
Synthetic peptide directed towards the N terminal region of human ZNF57
Other Notes
Synthetic peptide located within the following region: FTLEEWALLDSAQRDLYRDVMLETFRNLASVDDGTQFKANGSVSLQDMYG
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Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Asli Sirmaci et al.
PloS one, 7(2), e32000-e32000 (2012-03-01)
Whole exome sequencing provides unprecedented opportunities to identify causative DNA variants in rare Mendelian disorders. Finding the responsible mutation via traditional methods in families with hearing loss is difficult due to a high degree of genetic heterogeneity. In this study
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