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Antibodies

Ghitm Polyclonal Antibody

Product Sizes
50 ug
£302.00
CAC09780-50UG
100 ug
£454.00
CAC09780-100UG
About this Product
SKU:
CAC09780
Additional Names:
Dermal papilla derived protein 2|Dermal papilla-derived protein 2|DERP2|Ghitm|GHITM_HUMAN|Growth hormone inducible transmembrane protein|Growth hormone-inducible transmembrane protein|HSPC282|MICS1|Mitochondrial morphology and cristae structure 1|My021|PTD010|TMBIM5|Transmembrane BAX inhibitor motif containing 5|Transmembrane BAX inhibitor motif containing protein 5|Transmembrane BAX inhibitor motif-containing protein 5
Application:
ELISA, Immunofluorescence, Immunohistochemistry, Western Blot
Buffer:
0.01m PBS
CE/IVD:
RUO
translate.label.attr.clone:
Polyclonal
Clonality:
Polyclonal
Extra Details:
The Ghitm Polyclonal Antibody is applicable for the following applications: ELISA, WB, IHC, IF.
Host:
Rabbit
Immunogen:
GHITM
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: GHITM antibody at 2.7ug/ml; Secondary; Goat polyclonal to rabbit IgG at 1/50000 dilution; Predicted band size: 38 kDa; Observed band size: 38 kDa
IHC image diluted at 1:400 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.
IHC image diluted at 1:400 and staining in paraffin-embedded human pancreatic 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 HepG2 cells with CAC09780 at 1:133, 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).