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Rabbit anti-LMAN1 polyclonal antibody - middle region
Catalog Number:OM112574
OM112574
Discount Price
OM112574-100ul
1~2 Week
100ul
OM112574-50ul
50ul
OM112574-20ul
20ul
1~2 Week
Product Profile
Product Name Rabbit anti-LMAN1 polyclonal antibody - middle region
Antibody Type Primary Antibodies
Antigen Alias ERGIC-53, ERGIC53, F5F8D, FMFD1, MCFD1, MR60, gp58
Immunogen The immunogen for anti-LMAN1 antibody: synthetic peptide directed towards the middle region of human LMAN1
Key Feature
Clonality Polyclonal
Isotype IgG
Host Species Rabbit
Tested Applications WB
WB:1:500~1:2000
Notes:Optimal dilutions/concentrations should be determined by the researcher.
Species Reactivity BovineDogHorseHumanMousePigRabbitRatZebra Fish
Concentration 1mg/ml
Purification Protein A
Target Information
Gene Symbol LMAN1
Gene Synonyms ERGIC-53
ERGIC53
F5F8D
FMFD1
MCFD1
MR60
gp58
Gene Full Name Lectin, mannose-binding, 1
Gene Summary LMAN1 is a type I integral membrane protein localized in the intermediate region between the endoplasmic reticulum and the Golgi, presumably recycling between the two compartments. The protein is a mannose-specific lectin and is a member of a novel family of plant lectin homologs in the secretory pathway of animal cells. Mutations in its gene are associated with a coagulation defect. Using positional cloning, its gene was identified as the disease gene leading to combined factor V-factor VIII deficiency, a rare, autosomal recessive disorder in which both coagulation factors V and VIII are diminished.The protein encoded by this gene is a type I integral membrane protein localized in the intermediate region between the endoplasmic reticulum and the Golgi, presumably recycling between the two compartments. The protein is a mannose-specific lectin and is a member of a novel family of plant lectin homologs in the secretory pathway of animal cells. Mutations in the gene are associated with a coagulation defect. Using positional cloning, the gene was identified as the disease gene leading to combined factor V-factor VIII deficiency, a rare, autosomal recessive disorder in which both coagulation factors V and VIII are diminished.
Alternative Names ERGIC-53
ERGIC53
F5F8D
FMFD1
MCFD1
MR60
gp58
Molecular Weight(MW) 54kDa
Sequence 510 amino acids
Database Links
Entrez Gene 3998
SwissProt ID P49257
Protein Accession NP_005561
Application

Western blot

1.25ug/mlPositive Control: HepG2 cell lysate
Application Notes WB:1:500~1:2000
Notes:Optimal dilutions/concentrations should be determined by the researcher.
Additional Information
Form Liquid
Storage Instructions Aliquot and store at -20°C. Avoid repeated freeze / thaw cycles
Storage Buffer phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
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