Mouse Anti-EPS8L2 Recombinant Antibody (CBFYE-0245) (CBMAB-E0499-FY)

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Basic Information

Host Animal
Mouse
Clone
CBFYE-0245
Application
WB, ELISA, IP
Immunogen
Recombinant human Eps8L2.
Host Species
Mouse
Specificity
Human, Mouse, Rat
Antibody Isotype
IgG1, κ
Clonality
Monoclonal Antibody
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.
ApplicationNote
ELISA1:100-1:1,000
WB1:100-1:1,000
IP1-2 µg per 100-500 µg of total protein (1 ml of cell lysate)

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
PBS, gelatin
Preservative
Sodium azide
Concentration
Batch dependent
Purity
> 95% Purity determined by SDS-PAGE.
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.
Epitope
AA 615-715
More Infomation

Target

Full Name
EPS8-like 2
Introduction
This gene encodes a member of the EPS8 gene family. The encoded protein, like other members of the family, is thought to link growth factor stimulation to actin organization, generating functional redundancy in the pathways that regulate actin cytoskeletal remodeling.
Entrez Gene ID
UniProt ID
Alternative Names
EPS8 Like 2; Epidermal Growth Factor Receptor Pathway Substrate 8-Related Protein 2; EPS8-Related Protein 2; EPS8R2; Epidermal Growth Factor Receptor Kinase Substrate 8-Like Protein 2; EPS8-Like Protein 2; EPS8-Like 2; DFNB106
Research Area
Stimulates guanine exchange activity of SOS1. May play a role in membrane ruffling and remodeling of the actin cytoskeleton. In the cochlea, is required for stereocilia maintenance in adult hair cells (By similarity).
Biological Process
Positive regulation of ruffle assembly Source: UniProtKB
Regulation of catalytic activity Source: GOC
Regulation of Rho protein signal transduction Source: UniProtKB
Rho protein signal transduction Source: UniProtKB
Sensory perception of sound Source: UniProtKB
Cellular Location
Cytoplasm; Stereocilium. Localizes at the tips of the stereocilia of the inner and outer hair cells.
Involvement in disease
Deafness, autosomal recessive, 106 (DFNB106):
A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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