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  1. Alles ansehen
  2. Polyclonal

GTX33163

DPM1 antibody

Eine Lieferung in diese Region ist nicht möglich.

SKU:
GTX33163
Zusätzliche Namen:
dolichyl-phosphate mannosyltransferase subunit 1, catalytic , CDGIE , MPDS
Anwendung:
WB, IF, ICC
Physischer Zustand:
Liquid
Spezies-Reaktivität:
Human
Aufreinigung:
Affinity Purified
Lagerbedingungen:
-20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Hersteller:
Genetex
Host:
Rabbit
Reaktivitäten:
Human, Mouse, Rat
Buffer:
PBS, 50% Glycerol, 0.02% Sodium azide.
Immunogen:
Recombinant fusion protein containing a sequence corresponding to amino acids 1-260 of human DPM1 (NP_003850.1).
Uniprot:
O60762
Synonyme:
CDGIE;dolichol monophosphate mannose synthase;dolichol-phosphate mannose synthase subunit 1;dolichol-phosphate mannosyltransferase subunit 1;dolichyl-phosphate beta-D-mannosyltransferase subunit 1;dolichyl-phosphate mannosyltransferase polypeptide 1 catalytic subunit;DPM synthase complex, catalytic subunit;DPM synthase subunit 1;mannose-P-dolichol synthase subunit 1;MPD synthase subunit 1;MPDS
Weitere Details:
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. [provided by RefSeq, Nov 2015]
Versandbedingungen:
Blue Ice