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Antibodies

Hexa Polyclonal Antibody

Product Sizes
50 ug
£302.00
CAC11280-50UG
100 ug
£454.00
CAC11280-100UG
About this Product
SKU:
CAC11280
Additional Names:
Beta hexosaminidase alpha chain precursor|Beta hexosaminidase subunit alpha|Beta N acetylhexosaminidase|Beta N acetylhexosaminidase subunit alpha|Beta-hexosaminidase A|Beta-hexosaminidase subunit alpha|Beta-N-acetylhexosaminidase subunit alpha|Hexa|HEXA_HUMAN|Hexosaminidase A|Hexosaminidase A (alpha polypeptide)|Hexosaminidase A alpha polypeptide|Hexosaminidase subunit A|MGC99608|N acetyl beta glucosaminidase|N acetyl beta glucosaminidase subunit alpha|N-acetyl-beta-glucosaminidase subunit alpha|TSD
Application:
ELISA, Immunofluorescence, Immunohistochemistry, Western Blot
Buffer:
0.01m PBS
CE/IVD:
RUO
translate.label.attr.clone:
Polyclonal
Clonality:
Polyclonal
Extra Details:
The Hexa Polyclonal Antibody is applicable for the following applications: ELISA, WB, IHC, IF.
Host:
Rabbit
Immunogen:
HEXA
Isotype:
IgG
Physical State:
Liquid
Purification:
Protein G Purified
Reactivities:
Rat
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: Rat brain tissue; All lanes: HEXA antibody at 5.8ug/ml; Secondary; Goat polyclonal to rabbit IgG at 1/50000 dilution; Predicted band size: 61, 20 kDa; Observed band size: 61 kDa
IHC image diluted at 1:300 and staining in paraffin-embedded human endometrial cancer 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.
Immunofluorescence staining of PC-3 cells with CAC11280 at 1:100, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).