EPS8L2 Antibody

Code CSB-PA007753GA01HU
Size $600
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Product Details

Uniprot No.
Target Names
EPS8L2
Alternative Names
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
Raised in
Rabbit
Species Reactivity
Human,Mouse
Immunogen
Human EPS8L2
Immunogen Species
Homo sapiens (Human)
Isotype
IgG
Purification Method
Antigen Affinity purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
Tested Applications
ELISA,WB
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Function
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.
Gene References into Functions
  1. frame-shift variant (c.1014delC; p.Ser339Alafs*15) was identified in EPS8L2, encoding Epidermal growth factor receptor Pathway Substrate 8 L2, a protein of hair cells' stereocilia previously implicated in progressive deafness in the mouse PMID: 26282398
Involvement in disease
Deafness, autosomal recessive, 106 (DFNB106)
Subcellular Location
Cytoplasm. Cell projection, stereocilium.
Protein Families
EPS8 family
Tissue Specificity
Detected in fibroblasts and placenta.
Database Links

HGNC: 21296

OMIM: 614988

KEGG: hsa:64787

STRING: 9606.ENSP00000320828

UniGene: Hs.55016

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7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA
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