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Antibody used in WB on Human MCF7 at 0.2-1 ug/ml.
Antibody used in WB on Human Tonsil.
Antibody used in IHC on Human Tonsil at of 5 ug/ml.
Antibody used in WB on Human MCF7 at 0.2-1 ug/ml.

GSN Antibody

CATALOG NUMBER: 26-845

Clonality:
Polyclonal
Tested Applications:
ELISA, WB
Host Species:
Rabbit
Species Reactivity:
Human
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Human
Immunogen:
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human GSN.
Conjugate:
Unconjugated
Tested Applications:
ELISA, WB
Application Note:
GSN antibody can be used for detection of GSN by ELISA at 1:62500. GSN antibody can be used for detection of GSN by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Positive Control 1:
Cat. No. 1219 - MCF7 Cell Lysate
Predicted Molecular Weight:
83 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 GSN antibody at -20°C. As with any antibody avoid repeat freeze-thaw cycles.
Ncbi Official Symbol:
GSN
Additional Names:
GSN, DKFZp313L0718, ADF, AGEL
Protein Accession Number:
NP_000168
Protein Gi Number:
4504165
Ncbi Gene Id Number:
2934
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
GSN binds to the 'plus' ends of actin monomers and filaments to prevent monomer exchange. It is a calcium-regulated protein, which functions in both assembly and disassembly of actin filaments. Defects in the gene encoding GSN are a cause of familial amyloidosis Finnish type (FAF).The protein encoded by this gene binds to the 'plus' ends of actin monomers and filaments to prevent monomer exchange. The encoded calcium-regulated protein functions in both assembly and disassembly of actin filaments. Defects in this gene are a cause of familial amyloidosis Finnish type (FAF). Multiple transcript variants encoding several different isoforms have been found for this gene.
Background Reference 1:
Shokouhi, G. Nephrol. Dial. Transplant. 23 (3), 1071 (2008).

FOR RESEARCH USE ONLY

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

Disclaimer:
This product is for research use only.

CATALOG NUMBER:

26-845

List Size:
100 ul

List Price:

$519.00

Datasheet
Shipping Info

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