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EPS8L2 Antibody

CAT: 0399-CSB-PA007753GA01HUSize: 100 µLDry Ice: NoHazardous: No
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CAT#:0399-CSB-PA007753GA01HUSize:100 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Gene Aliases
Epidermal growth factor receptor kinase substrate 8 like protein 2 antibody; Epidermal growth factor receptor kinase substrate 8-like protein 2 antibody; Epidermal growth factor receptor pathway substrate 8 like protein 2 antibody; Epidermal growth factor receptor pathway substrate 8 related protein 2 antibody; Epidermal growth factor receptor pathway substrate 8-related protein 2 antibody; EPS8 like 2 antibody; EPS8 like protein 2 antibody; EPS8 related protein 2 antibody; EPS8-like protein 2 antibody; EPS8-related protein 2 antibody; EPS8L 2 antibody; EPS8L2 antibody; EPS8R 2 antibody; EPS8R2 antibody; ES8L2_HUMAN antibody; FLJ16738 antibody; FLJ21935 antibody; FLJ22171 antibody; MGC126530 antibody; MGC3088 antibody
UniProt
Q9H6S3
Host
Rabbit
Antigen Species
Human
Reactivity
Human, Mouse
Target Antigen
Human EPS8L2
Target
EPS8L2
Clonality
Polyclonal
Conjugation
Non-conjugated
Field of Research
Signal Transduction
Purification Method
Antigen Affinity Purified
Form
Liquid
Buffer
PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
Storage Conditions
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Antibody Type
Polyclonal Antibody
Tested Applications
ELISA, WB
Isotype
IgG

UniProtKB · Q9H6S3

Epidermal growth factor receptor kinase substrate 8-like protein 2

ES8L2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9H6S3
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
EPS8L2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
EPS8-like protein 2
EC number
—
Processing
—
Secondary accessions
B3KSX1, B7ZKL3, Q53GM8, Q8WYW7, Q96K06, Q9H6K9
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Cellular component

Cell projectionCytoplasm

Disease

DeafnessNon-syndromic deafness

PTM

Phosphoprotein

Domain

SH3 domain

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