FKTN (DGR36108) Rabbit mAb - diagbio | 戴格生物

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Recombinant DGRmAb^®

FKTN (DGR36108) Rabbit mAb

db16343

Datasheet

Product Name : FKTN (DGR36108) Rabbit mAb

Cat.No.: db16343

Synonyms : FCMD; CMD1X; LGMD2M; MDDGA4; MDDGB4; MDDGC4; LGMDR13

Application：

Reactivity : Human, Mouse, Rat

Host species : Rabbit

Un-conjugated

Background The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2010]
Immunogen A synthetic peptide of Human FKTN
Gene ID 2218
Swiss Prot O75072
Synonyms FCMD; CMD1X; LGMD2M; MDDGA4; MDDGB4; MDDGC4; LGMDR13
Reactivity Human, Mouse, Rat
Application WB, IHC-P
Recommended dilution WB: 1:1000-1:5000
IHC-P: 1:100-1:200
Calculated MW 54 kDa
Observed MW 54 kDa
Host species Rabbit
Clonality Monoclonal
Clonality No. DGR36108
Isotype IgG
Purity Affinity Purification
Conjugation Un-conjugated
Storage/Stability Store at -20°C. Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt.

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