ALG9 anticorps (Middle Region)
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- Antigène Voir toutes ALG9 Anticorps
- ALG9 (Asparagine-Linked Glycosylation 9, alpha-1,2-Mannosyltransferase (ALG9))
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Épitope
- Middle Region
- Reactivité
- Humain, Souris, Boeuf (Vache), Chien, Cheval, Lapin, Rat, Cobaye, Poisson zèbre (Danio rerio)
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp ALG9 est non-conjugé
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Application
- Western Blotting (WB)
- Séquence
- LLVLPLTSLM EYLLQRFHVQ NLGHPYWLTL APMYIWFIIF FIQPHKEERF
- Homologie
- Cow: 100%, Dog: 100%, Guinea Pig: 93%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%, Zebrafish: 91%
- Attributs du produit
- This is a rabbit polyclonal antibody against ALG9. It was validated on Western Blot.
- Purification
- Affinity Purified
- Immunogène
- The immunogen is a synthetic peptide directed towards the middle region of Human ALG9
- Top Product
- Discover our top product ALG9 Anticorps primaire
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- Indications d'application
- Optimal working dilution should be determined by the investigator.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- Antigène
- ALG9 (Asparagine-Linked Glycosylation 9, alpha-1,2-Mannosyltransferase (ALG9))
- Autre désignation
- ALG9 (ALG9 Produits)
- Synonymes
- anticorps CDG1L, anticorps DIBD1, anticorps LOH11CR1J, anticorps 8230402H15Rik, anticorps AI747665, anticorps B430313H07Rik, anticorps Dibd1, anticorps ALG9, alpha-1,2-mannosyltransferase, anticorps asparagine-linked glycosylation 9 (alpha 1,2 mannosyltransferase), anticorps ALG9, anticorps Alg9
- Sujet
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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.
Alias Symbols: ALG9, DIBD1,
Protein Interaction Partner: UBC, BHMT, H2AFX,
Protein Size: 447 - ID gène
- 79796
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