SAB4301803
Anti-TIA1
affinity isolated antibody
Synonym(s):
TIA-1
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About This Item
NACRES:
NA.41
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
polyclonal
Application:
immunohistochemistry
western blot
western blot
Species reactivity:
human
Citations:
3
Technique(s):
immunohistochemistry: 1: 100-250
western blot: 1:500-1:2000
western blot: 1:500-1:2000
Uniprot accession no.:
Product Name
Anti-TIA1, affinity isolated antibody
biological source
rabbit
conjugate
unconjugated
antibody form
affinity isolated antibody
antibody product type
primary antibodies
clone
polyclonal
form
buffered aqueous glycerol solution
species reactivity
human
technique(s)
immunohistochemistry: 1: 100-250
western blot: 1:500-1:2000
accession no.
BC015944
UniProt accession no.
shipped in
wet ice
storage temp.
−20°C
target post-translational modification
unmodified
Quality Level
Gene Information
human ... TIA1(7072)
Features and Benefits
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Immunogen
Full length fusion protein
Physical form
Rabbit IgG in pH7.4 PBS, 0.05% NaN3, 40% Glycerol.
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Storage Class
10 - Combustible liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Triana Amen et al.
Cell reports, 35(11), 109237-109237 (2021-06-17)
The formation of stress granules (SGs) is an essential aspect of the cellular response to many kinds of stress, but its adaptive role is far from clear. SG dysfunction is implicated in aging-onset neurodegenerative diseases, prompting interest in their physiological
Triana Amen et al.
Molecular biology of the cell, 32(21), ar18-ar18 (2021-08-26)
Stress granules (SGs) are ribonucleoprotein functional condensates that form under stress conditions in all eukaryotic cells. Although their stress-survival function is far from clear, SGs have been implicated in the regulation of many vital cellular pathways. Consequently, SG dysfunction is
Triana Amen et al.
Frontiers in cell and developmental biology, 8, 606111-606111 (2021-05-12)
Metabolic regulation is a necessary component of all stress response pathways, because all different mechanisms of stress-adaptation place high-energy demands on the cell. Mechanisms that integrate diverse stress response pathways with their metabolic components are therefore of great interest, but
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