ALG2 anticorps (AA 254-282)
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- Antigène Voir toutes ALG2 Anticorps
- ALG2 (Asparagine-Linked Glycosylation 2, alpha-1,3-Mannosyltransferase Homolog (ALG2))
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Épitope
- AA 254-282
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp ALG2 est non-conjugé
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Application
- Western Blotting (WB)
- Purification
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- Immunogène
- This ALG2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 254-282 amino acids from the Central region of human ALG2.
- Clone
- RB36980
- Isotype
- Ig Fraction
- Top Product
- Discover our top product ALG2 Anticorps primaire
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- Indications d'application
- WB: 1:1000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
- 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
- 4 °C,-20 °C
- Stockage commentaire
- ALG2 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
- Date de péremption
- 6 months
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- Antigène
- ALG2 (Asparagine-Linked Glycosylation 2, alpha-1,3-Mannosyltransferase Homolog (ALG2))
- Autre désignation
- ALG2 (ALG2 Produits)
- Synonymes
- anticorps CDGIi, anticorps NET38, anticorps hALPG2, anticorps 1110018A23Rik, anticorps 1300013N08Rik, anticorps ALPG2, anticorps MNCb-5081, anticorps im:7145131, anticorps ALG2, alpha-1,3/1,6-mannosyltransferase, anticorps asparagine-linked glycosylation 2 (alpha-1,3-mannosyltransferase), anticorps ALG2, alpha-1,3/1,6-mannosyltransferase L homeolog, anticorps GDP-Man:Man(1)GlcNAc(2)-PP-dolichol alpha-1,3-mannosyltransferase, anticorps ALG2, anticorps Alg2, anticorps alg2.L, anticorps alg2
- Sujet
- This gene encodes a member of the glycosyltransferase 1 family. The encoded protein acts as an alpha 1,3 mannosyltransferase, mannosylating Man(2)GlcNAc(2)-dolichol diphosphate and Man(1)GlcNAc(2)-dolichol diphosphate to form Man(3)GlcNAc(2)-dolichol diphosphate. Defects in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ii). Alternative splicing results in multiple transcript variants.
- Poids moléculaire
- 47092
- ID gène
- 85365
- NCBI Accession
- NP_149078
- UniProt
- Q9H553
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