Comparison

LFNG Antibody

Item no. PRS-26-024-100ul
Manufacturer ProSci
Amount 100 ul
Category
Type Antibody Polyclonal
Format Liquid
Applications WB, ELISA
Specific against Human, Mouse, Rat
Host Rabbit
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias LFNG, SCDO3
Available
Shipping
blue ice or RT
By Research Area
Membrane
Immunogen
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human LFNG.
Applications
LFNG antibody can be used for detection of LFNG by ELISA at 1:62500. LFNG antibody can be used for detection of LFNG by western blot at 1 μ g/mL, and HRP conjugated secondary antibody should be diluted 1:50, 000 - 100, 000.
Positive Control 1
Cat. No. XBL-10413 - Fetal Skeletal Muscle Tissue Lysate
Predicted Molecular Weight
39 kDa
Purification
Antibody is purified by peptide affinity chromatography method.
Clonality
Polyclonal
Conjugate
Unconjugated
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 LFNG antibody at -20˚ C. As with any antibody avoid repeat freeze-thaw cycles.
Disclaimer
This product is for research use only.
Modifications
None
Ncbi Official Symbol
LFNG
Accession #
NP_001035258
Protein Gi #
93141005
Ncbi Gene Id #
3955
User Note
Optimal dilutions for each application to be determined by the researcher.
Ncbi Official Symbol
LFNG
Ncbi Official Full Name
LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
Ncbi Organism
Homo sapiens
Swissprot #
Q8NES3-3
Background
LFNG is a member of the glycosyltransferase superfamily. It is a single-pass type II Golgi membrane protein that functions as a fucose-specific glycosyltransferase, adding an N-acetylglucosamine to the fucose residue of a group of signaling receptors involved in regulating cell fate decisions during development. Mutations in the gene that encodes this protein have been associated with autosomal recessive spondylocostal dysostosis 3. This gene encodes a member of the glycosyltransferase superfamily. The encoded protein is a single-pass type II Golgi membrane protein that functions as a fucose-specific glycosyltransferase, adding an N-acetylglucosamine to the fucose residue of a group of signaling receptors involved in regulating cell fate decisions during development. Mutations in this gene have been associated with autosomal recessive spondylocostal dysostosis 3. Alternatively spliced transcript variants that encode different isoforms have been described, however, not all variants have been fully characterized.
Background References 1
Sparrow, D.B., (2006) Am. J. Hum. Genet. 78 (1), 28-37.
1st Image Caption
Antibody used in WB on Human Muscle at 0.2-1 ug/ml.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 100 ul
Available: In stock
available

Compare

Add to wishlist

Get an offer

Request delivery time

Ask a technical question

Submit a bulk request

Questions about this Product?
 
Close