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POMGNT1 antibody
POMGNT1
Reactivity: Human, Mouse, Rat
IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-POMGNT1 Antibody
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Target
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POMGNT1
(Protein O-Linked Mannose Beta1,2-N-Acetylglucosaminyltransferase (POMGNT1))
Reactivity
All reactivities for POMGNT1 antibodies
Human, Mouse, Rat
Host
All hosts for POMGNT1 antibodies
Rabbit
Clonality
All clonalities for POMGNT1 antibodies
Polyclonal
Conjugate
All conjugates for POMGNT1 antibodies
This POMGNT1 antibody is un-conjugated
Application
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Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Recombinant fusion protein of human POMGNT1 (NP_060209.3).
Isotype
IgG
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Alternatives
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Application Details
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Application Notes
IHC 1:50-1:100
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
1 mg/mL
Buffer
PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for POMGNT1
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Target
POMGNT1
(Protein O-Linked Mannose Beta1,2-N-Acetylglucosaminyltransferase (POMGNT1))
Alternative Name
POMGNT1 (POMGNT1 Products )
Synonyms
POMGNT1 antibody, im:7151461 antibody, zgc:158130 antibody, 0610016I07Rik antibody, 4930467B06Rik antibody, GNTI.2 antibody, GnT I.2 antibody, LGMD2O antibody, MDDGA3 antibody, MDDGB3 antibody, MDDGC3 antibody, MEB antibody, MGAT1.2 antibody, gnT-I.2 antibody, protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) antibody, protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) S homeolog antibody, protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase antibody, POMGNT1 antibody, pomgnt1.S antibody, pomgnt1 antibody, Pomgnt1 antibody
Background
This gene encodes a type II transmembrane protein that resides in the Golgi apparatus. It participates in O-mannosyl glycosylation and is specific for alpha linked terminal mannose. Mutations in this gene may be associated with muscle-eye-brain disease and several congenital muscular dystrophies. Alternatively spliced transcript variants that encode different protein isoforms have been described.
Gene ID
55624
UniProt
Q8WZA1
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