ALG11 anticorps (C-Term)
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- Antigène Voir toutes ALG11 Anticorps
- ALG11 (Asparagine-Linked Glycosylation 11, alpha-1,2-Mannosyltransferase Homolog (Yeast) (ALG11))
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Épitope
- C-Term
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Reactivité
- Humain, Souris, Rat, Cheval, Lapin, Chien, Boeuf (Vache), Cobaye, Saccharomyces cerevisiae, Poisson zèbre (Danio rerio)
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp ALG11 est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (IHC)
- Séquence
- LHTMWNEHFG IGVVECMAAG TIILAHNSGG PKLDIVIPHE GDITGFLAES
- Homologie
- Cow: 92%, Dog: 86%, Guinea Pig: 93%, Horse: 100%, Human: 93%, Mouse: 100%, Rabbit: 86%, Rat: 100%, Yeast: 92%, Zebrafish: 91%
- Attributs du produit
- This is a rabbit polyclonal antibody against ALG11. It was validated on Western Blot and immunohistochemistry.
- Purification
- Affinity Purified
- Immunogène
- The immunogen is a synthetic peptide directed towards the C terminal region of human ALG11
- Top Product
- Discover our top product ALG11 Anticorps primaire
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- Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator.
- Commentaires
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Antigen size: 492 AA
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- Lot specific
- 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.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- 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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A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip." dans: Human molecular genetics, Vol. 19, Issue 8, pp. 1413-24, (2010) (PubMed).
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A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip." dans: Human molecular genetics, Vol. 19, Issue 8, pp. 1413-24, (2010) (PubMed).
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- Antigène
- ALG11 (Asparagine-Linked Glycosylation 11, alpha-1,2-Mannosyltransferase Homolog (Yeast) (ALG11))
- Autre désignation
- ALG11 (ALG11 Produits)
- Synonymes
- anticorps UTP14C, anticorps CDG1P, anticorps GT8, anticorps RGD1564725, anticorps AI849156, anticorps AW492253, anticorps B230397C21, anticorps si:dkey-1h24.5, anticorps wu:fj04e04, anticorps asparagine-linked glycosylation 11, alpha-1,2-mannosyltransferase, anticorps ALG11, alpha-1,2-mannosyltransferase, anticorps ALG11, alpha-1,2-mannosyltransferase L homeolog, anticorps asparagine-linked glycosylation 11 (alpha-1,2-mannosyltransferase), anticorps alg11, anticorps ALG11, anticorps alg11.L, anticorps Alg11
- Sujet
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The function remains unknown.
Alias Symbols: GT8, KIAA0266, CDG1P
Protein Interaction Partner: UBC,
Protein Size: 492 - Poids moléculaire
- 56 kDa
- ID gène
- 440138
- NCBI Accession
- NM_001004127, NP_001004127
- UniProt
- Q2TAA5
- Pathways
- SARS-CoV-2 Protein Interactome
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