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Antibodies

Celf2 Polyclonal Antibody

Product Sizes
50 ug
£302.00
CAC07980-50UG
100 ug
£454.00
CAC07980-100UG
About this Product
SKU:
CAC07980
Additional Names:
Bruno-like protein 3|BRUNOL3|Cardiac elav type RNA binding protein|CELF-2|celf2|CELF2_HUMAN|CUG BP2|CUG triplet repeat RNA-binding protein 2|CUG-BP- and ETR-3-like factor 2|CUG-BP2|CUGBP Elav like family member 2|CUGBP Elav-like family member 2|CUGBP2|dJ323N1.1|elav type RNA binding protein|ELAV-type RNA-binding protein 3|ETR 3|ETR-3|ETR3|HGNC:2550|hNAPOR|NAPOR|NAPOR 2|Neuroblastoma apoptosis-related RNA-binding protein|Neuroplastoma apoptosis related RNA binding protein 3|RNA binding protein BRUNOL3|RNA-binding protein BRUNOL-3
Application:
ELISA, Immunofluorescence, Immunohistochemistry, Western Blot
Buffer:
0.01m PBS
CE/IVD:
RUO
translate.label.attr.clone:
Polyclonal
Clonality:
Polyclonal
Extra Details:
The Celf2 Polyclonal Antibody is applicable for the following applications: ELISA, WB, IHC, IF.
Host:
Rabbit
Immunogen:
CELF2
Isotype:
IgG
Physical State:
Liquid
Purification:
Protein G Purified
Shipping Conditions:
Blue Ice
Source:
Rabbit
Storage Conditions:
-20[o]C Avoid freeze/thaw cycles., 2-8[o]C Avoid freeze/thaw cycles.
Supplier:
Biomatik
Type:
Antibody: Polyclonal Antibody
Catalog Antibody.JPG
Western Blot; Positive WB detected in: K562 whole cell lysate, A549 whole cell lysate; All lanes: CELF2 antibody at 3ug/ml; Secondary; Goat polyclonal to rabbit IgG at 1/50000 dilution; Predicted band size: 55, 53, 56 kDa; Observed band size: 55 kDa
IHC image diluted at 1:600 and staining in paraffin-embedded human tonsil tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
IHC image diluted at 1:600 and staining in paraffin-embedded human brain tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
Immunofluorescent analysis of A549 cells using CAC07980 at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)