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Antibody used in IHC on human skeletal muscle at 5.0 ug/ml.
Antibody used in WB on Human 721_B at 0.2-1 ug/ml.
Antibody used in IHC on Mouse Cerebellum.
Antibody used in WB on Hum. Adult Placenta at 1 ug/ml.
Antibody used in WB on Hum. Fetal Liver at 1 ug/ml.
Antibody used in WB on Human 721_B at 1 ug/ml.
Antibody used in IHC on human skeletal muscle at 5.0 ug/ml.

SGCE Antibody

CATALOG NUMBER: 26-132

Clonality:
Polyclonal
Tested Applications:
ELISA, WB
Host Species:
Rabbit
Species Reactivity:
Human, Mouse, Rat
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Human, Mouse, Rat
Immunogen:
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SGCE.
Conjugate:
Unconjugated
Tested Applications:
ELISA, WB
Application Note:
SGCE antibody can be used for detection of SGCE by ELISA at 1:312500. SGCE antibody can be used for detection of SGCE by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Positive Control 1:
721_B Cell Lysate
Predicted Molecular Weight:
52 kDa
Purification:
Antibody is purified by peptide affinity chromatography method.
Clonality:
Polyclonal
Physical State:
Liquid
Buffer:
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Concentration:
batch dependent
Storage Conditions:
For short periods of storage (days) store at 4°C. For longer periods of storage, store SGCE antibody at -20°C. As with any antibody avoid repeat freeze-thaw cycles.
Ncbi Official Symbol:
SGCE
Additional Names:
SGCE, DYT11, ESG
Protein Accession Number:
NP_001092871
Protein Gi Number:
150378454
Ncbi Gene Id Number:
8910
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
SGCE is a member of the sarcoglycan family. Sarcoglycans are transmembrane components in the dystrophin-glycoprotein complex which help stabilize the muscle fiber membranes and link the muscle cytoskeleton to the extracellular matrix. Mutations in this gene have been associated with myoclonus-dystonia syndrome. Alternative splicing results in multiple transcript variants.The SGCE gene encodes the epsilon member of the sarcoglycan family, transmembrane components of the dystrophin-glycoprotein complex, which links the cytoskeleton to the extracellular matrix.
Background Reference 1:
Hjermind, L.E., (2008) Eur. J. Neurol. 15 (5), 525-529.

FOR RESEARCH USE ONLY

For additional information, visit ProSci’s Terms & Conditions Page.

Disclaimer:
This product is for research use only.

CATALOG NUMBER:

26-132

List Size:
100 ul

List Price:

$519.00

Datasheet
Shipping Info

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