REEP1 polyclonal, anti-human, mouse, rat
€388.00
In stock
SKU
BS70947
Background:
This gene encodes a mitochondrial protein that functions to enhance the cell surface expression of odorant receptors. Mutations in this gene cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. Alternative splicing results in multiple transcript variants.
Alternative Name:
HMN5B, SPG31, C2orf23,
Application Dilution: WB: 1:500 - 1:2000, IF: 1:50 - 1:200
Specificity: REEP1 polyclonal antibody detects endogenous levels of REEP1 protein.
Immunogen:
Recombinant protein of human REEP1.
MW: ~ 22 kDa
Swis Prot.: Q9H902
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 with 0.02% sodium azide, 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 mitochondrial protein that functions to enhance the cell surface expression of odorant receptors. Mutations in this gene cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. Alternative splicing results in multiple transcript variants.
Alternative Name:
HMN5B, SPG31, C2orf23,
Application Dilution: WB: 1:500 - 1:2000, IF: 1:50 - 1:200
Specificity: REEP1 polyclonal antibody detects endogenous levels of REEP1 protein.
Immunogen:
Recombinant protein of human REEP1.
MW: ~ 22 kDa
Swis Prot.: Q9H902
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 with 0.02% sodium azide, 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.
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