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DPM1 Antibody (HRP)

CAT: 0013-GTR17883352-01Size: 50 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR17883352-01Size:50 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
This DPM1 Antibody, HRP conjugated is an HRP polyclonal product. It tagets DPM1 using a Recombinant Human Dolichol-phosphate mannosyltransferase subunit 1 protein (2-260AA) as the immunogen. This antibody is suitable for ELISA. Purification: >95%, Protein G purified.
Product Name Alternative
CDGIE antibody; dolichol monophosphate mannose synthase antibody; Dolichol phosphate mannose synthase antibody; Dolichol-phosphate mannose synthase antibody; Dolichol-phosphate mannosyltransferase antibody; Dolichyl phosphate beta D mannosyltransferase antibody; dolichyl phosphate mannosyltransferase polypeptide 1 antibody; dolichyl phosphate mannosyltransferase polypeptide 1 catalytic subunit antibody; Dolichyl-phosphate beta-D-mannosyltransferase antibody; DPM synthase antibody; DPM1 antibody; DPM1_HUMAN antibody; Mannose P dolichol synthase antibody; Mannose-P-dolichol synthase antibody; MPD synthase antibody; MPDS antibody
UniProt
O60762
Reactivity
Human
Immunogen
Recombinant Human Dolichol-phosphate mannosyltransferase subunit 1 protein (2-260AA)
Target
DPM1
Clonality
Polyclonal
Conjugation
HRP
Field of Research
Cell Biology
Purification
>95%, Protein G purified
Dilution
ELISA
Form
Liquid
Storage Conditions
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Notes
For research use only.
Tested Applications
ELISA
Host or Source
Rabbit
Preservative
Preservative: 0.03% Proclin 300. Constituents: 50% Glycerol
Isotype
IgG

UniProtKB · O60762

Dolichol-phosphate mannosyltransferase subunit 1

DPM1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
O60762
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
DPM1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
2.4.1.83
Processing
—
Secondary accessions
O15157, Q6IB78, Q96HK0
Protein keywords

PTM

AcetylationPhosphoprotein

Disease

Congenital disorder of glycosylationCongenital muscular dystrophyDisease variantDystroglycanopathy

Cellular component

Endoplasmic reticulum

Molecular function

GlycosyltransferaseTransferase

Ligand

MagnesiumManganeseMetal-binding

Technical term

Proteomics identificationReference proteome

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