Products for Research Use Only

EPS8 Rabbit Polyclonal Antibody (HRP)

CAT: 0013-GTR18678716Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18678716Size:100 µg
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Description
EPS8 Rabbit Polyclonal Antibody (HRP)
Product Name Alternative
Epidermal growth factor receptor kinase substrate 8
UniProt
Q12929
Reactivity
Human
Cross Reactivity
No cross-reactivity with other proteins
Immunogen
E.coli-derived human EPS8 recombinant protein (Position: Q255-E802) . Human EPS8 shares 88% and 89.1% amino acid (aa) sequence identity with mouse and rat EPS8, respectively.
Target
Epidermal growth factor receptor kinase substrate 8
Clonality
Polyclonal
Conjugation
HRP
Field of Research
Neuroscience
Purification
Immunogen affinity purified.
Dilution
Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.
Form
Liquid
Molecular Weight
92 kDa
Storage Conditions
At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
Notes
For research use only.
Tested Applications
ELISA, IHC, WB
Host or Source
Rabbit
Preservative
Each vial contains 50% glycerol, 0.9% NaCl, 0.2% Na2HPO4.
Isotype
Rabbit IgG

UniProtKB · Q12929

Epidermal growth factor receptor kinase substrate 8

EPS8_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q12929
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
EPS8
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
A6NMC3, A8K6W2, A8KA66, B4DX66, Q8N6J0
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Molecular function

Actin-binding

Coding sequence diversity

Alternative splicing

Cellular component

Cell membraneCell projectionCytoplasmMembraneSynapseSynaptosome

Disease

DeafnessNon-syndromic deafness

PTM

PhosphoproteinUbl conjugation

Domain

SH3 domain