DPM1 Antibody
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


DPM1 Antibody
Background :
Dolichol-phosphate mannose (Dol-P-Man) serves as a donor of mannosyl residues on the lumenal side of the endoplasmic reticulum (ER) . Lack of Dol-P-Man results in defective surface expression of GPI-anchored proteins. Dol-P-Man is synthesized from GDP-mannose and dolichol-phosphate on the cytosolic side of the ER by the enzyme dolichyl-phosphate mannosyltransferase. Human DPM1 lacks a carboxy-terminal transmembrane domain and signal sequence and is regulated by DPM2. Mutations in this gene are associated with congenital disorder of glycosylation type Ie. Alternative splicing results in multiple transcript variants.NCBI Gene ID :
8813Swiss Prot :
O60762Host :
RabbitReactivity :
Human, Mouse, RatImmunogen :
Recombinant fusion protein containing a sequence corresponding to amino acids 1-260 of human DPM1 (NP_003850.1) .Clonality :
PolyclonalConjugation :
UnconjugatedType :
Primary AntibodiesField of Research :
OtherPurification :
Affinity purificationPositive Control :
NCI-H460Concentration :
Batch dependentBuffer :
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.Modification :
NoneShipping Conditions :
Blue IceStorage Conditions :
Store at -20˚ C. Avoid freeze / thaw cycles.Calculated Molecular Weight :
Observed: 30kDaFragment :
IgGSymbol :
DPM1Positive Control 2 :
HeLaPositive Control 3 :
SKOV3Positive Control 4 :
Mouse pancreasPositive Control 5 :
Mouse liverPositive Control 6 :
Mouse kidneyNCBI Official Name :
Dolichyl-phosphate mannosyltransferase polypeptide 1, catalytic subunitNCBI Organism :
Homo sapiensOther Product Names :
DPM1, dolichyl-phosphate mannosyltransferase polypeptide 1, catalytic subunit, CDGIE, MPDS, dolichol monophosphate mannose synthaseTested Applications :
WB, IFPhysical Properties :
Liquid

