ALG9 antibody
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- Target See all ALG9 Antibodies
- ALG9 (Asparagine-Linked Glycosylation 9, alpha-1,2-Mannosyltransferase (ALG9))
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Reactivity
- Human, Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This ALG9 antibody is un-conjugated
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Application
- ELISA, Immunohistochemistry (IHC)
- Purification
- Affinity purification
- Immunogen
- Recombinant protein of human ALG9
- Isotype
- IgG
- Top Product
- Discover our top product ALG9 Primary Antibody
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anti-Asparagine-Linked Glycosylation 9, alpha-1,2-Mannosyltransferase (ALG9) (AA 434-618) antibody
ALG9 Reactivity: Human ELISA, IHC, WB Host: Rabbit Polyclonal unconjugated
anti-Asparagine-Linked Glycosylation 9, alpha-1,2-Mannosyltransferase (ALG9) antibodyALG9 Reactivity: Human, Mouse ELISA, IHC Host: Rabbit Polyclonal unconjugated
anti-Asparagine-Linked Glycosylation 9, alpha-1,2-Mannosyltransferase (ALG9) (AA 439-618) antibodyALG9 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
anti-Asparagine-Linked Glycosylation 9, alpha-1,2-Mannosyltransferase (ALG9) (Middle Region) antibodyALG9 Reactivity: Human, Mouse, Rabbit, Rat, Cow, Dog, Horse, Guinea Pig, Zebrafish (Danio rerio) WB Host: Rabbit Polyclonal unconjugated
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- Application Notes
- IHC 1:50-1:200
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.3 mg/mL
- Buffer
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
- Preservative
- Sodium azide
- Handling Advice
- Avoid freeze / thaw cycles.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- ALG9 (Asparagine-Linked Glycosylation 9, alpha-1,2-Mannosyltransferase (ALG9))
- Alternative Name
- ALG9 (ALG9 Products)
- Synonyms
- CDG1L antibody, DIBD1 antibody, LOH11CR1J antibody, 8230402H15Rik antibody, AI747665 antibody, B430313H07Rik antibody, Dibd1 antibody, ALG9, alpha-1,2-mannosyltransferase antibody, asparagine-linked glycosylation 9 (alpha 1,2 mannosyltransferase) antibody, ALG9 antibody, Alg9 antibody
- Background
- This gene encodes an alpha-1,2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have been found for this gene.
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