AFG3L2 polyclonal, anti-human, mouse
€388.00
In stock
SKU
BS72587
Background:
This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.
Alternative Name:
SCA28,SPAX5
Application Dilution: WB: 1:200 - 1:2000
Specificity: AFG3L2 polyclonal antibody detects endogenous levels of AFG3L2 protein.
Immunogen:
Recombinant protein of human AFG3L2
MW: ~ 89 kDa
Swis Prot.: Q9Y4W6
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:
1 mg/ml in Phosphate buffered saline (PBS) with 0.05% sodium azide, approx. pH 7.2.
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 localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.
Alternative Name:
SCA28,SPAX5
Application Dilution: WB: 1:200 - 1:2000
Specificity: AFG3L2 polyclonal antibody detects endogenous levels of AFG3L2 protein.
Immunogen:
Recombinant protein of human AFG3L2
MW: ~ 89 kDa
Swis Prot.: Q9Y4W6
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:
1 mg/ml in Phosphate buffered saline (PBS) with 0.05% sodium azide, approx. pH 7.2.
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