WBSCR27 polyclonal, anti-human, mouse
€388.00
In stock
SKU
BS72863
Background:
This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23.
Alternative Name:
WBSCR27
Application Dilution: WB: 1:500 - 1:2000
Specificity: WBSCR27 polyclonal antibody detects endogenous levels of WBSCR27 protein.
Immunogen:
Recombinant protein of human WBSCR27
MW: 26kDa
Swis Prot.: Q8N6F8
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS, 50% glycerol, pH7.3.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23.
Alternative Name:
WBSCR27
Application Dilution: WB: 1:500 - 1:2000
Specificity: WBSCR27 polyclonal antibody detects endogenous levels of WBSCR27 protein.
Immunogen:
Recombinant protein of human WBSCR27
MW: 26kDa
Swis Prot.: Q8N6F8
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS, 50% glycerol, pH7.3.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
| Is Featured? | No |
|---|
Write Your Own Review