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Antibody used in WB on Human 293T at 0.2-1 ug/ml.
Antibody used in WB on Human 293T at 0.2-1 ug/ml.

GLMN Antibody

CATALOG NUMBER: 26-651

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 GLMN.
Conjugate:
Unconjugated
Tested Applications:
ELISA, WB
Application Note:
GLMN antibody can be used for detection of GLMN by ELISA at 1:2500. GLMN antibody can be used for detection of GLMN by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Positive Control 1:
293T Cell Lysate
Predicted Molecular Weight:
68 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 GLMN antibody at -20°C. As with any antibody avoid repeat freeze-thaw cycles.
Ncbi Official Symbol:
GLMN
Additional Names:
GLMN, FAP, FAP48, FAP68, FKBPAP, GLML, GVM, VMGLOM
Protein Accession Number:
NP_444504
Protein Gi Number:
16933537
Ncbi Gene Id Number:
11146
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
GLMN is a phosphorylated protein that is a member of a Skp1-Cullin-F-box-like complex. The protein is essential for normal development of the vasculature and mutations in this gene have been associated with glomuvenous malformations, also called glomangiomas. Alternatively spliced variants that encode different protein isoforms have been described but the full-length nature of only one has been determined.This gene encodes a phosphorylated protein that is a member of a Skp1-Cullin-F-box-like complex. The protein is essential for normal development of the vasculature and mutations in this gene have been associated with glomuvenous malformations, also called glomangiomas. Alternatively spliced variants that encode different protein isoforms have been described but the full-length nature of only one has been determined. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Background Reference 1:
Arai, T., (2003) Proc. Natl. Acad. Sci. U.S.A. 100 (17), 9855-9860.

FOR RESEARCH USE ONLY

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

Disclaimer:
This product is for research use only.

CATALOG NUMBER:

26-651

List Size:
100 ul

List Price:

$519.00

Datasheet
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