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ALG11 anticorps (AA 301-385)

ALG11 Reactivité: Humain ELISA, IHC (p), IF (cc), IF (p), IHC (fro) Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN872969
  • Antigène Voir toutes ALG11 Anticorps
    ALG11 (Asparagine-Linked Glycosylation 11, alpha-1,2-Mannosyltransferase Homolog (Yeast) (ALG11))
    Épitope
    • 9
    • 8
    • 7
    • 7
    • 5
    • 1
    • 1
    • 1
    AA 301-385
    Reactivité
    • 40
    • 21
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 40
    Lapin
    Clonalité
    • 40
    Polyclonal
    Conjugué
    • 14
    • 5
    • 5
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp ALG11 est non-conjugé
    Application
    • 27
    • 24
    • 4
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
    Homologie
    Human,Mouse,Rat,Dog,Horse
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human ALG11
    Isotype
    IgG
    Top Product
    Discover our top product ALG11 Anticorps primaire
  • Indications d'application
    ELISA 1:500-1000
    IHC-P 1:200-400
    IHC-F 1:100-500
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
    Agent conservateur
    ProClin
    Précaution d'utilisation
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Stock
    4 °C,-20 °C
    Stockage commentaire
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    Date de péremption
    12 months
  • 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

    Synonyms: Asparagine-linked glycosylation protein 11 homolog, AI849156, alg11, ALG11_HUMAN, Asparagine-linked glycosylation 11, Asparagine-linked glycosylation 11, alpha-1,2-mannosyltransferase homolog yeast, GT8, UTP14C.

    Background: Mannosyltransferase involved in the last steps of the synthesis of Man5GlcNAc(2)-PP-dolichol core oligosaccharide on the cytoplasmic face of the endoplasmic reticulum. Catalyzes the addition of the 4th and 5th mannose residues to the dolichol-linked oligosaccharide chain.Involvement in disease:Defects in ALG11 are the cause of congenital disorder of glycosylation type 1P (CDG1P). A multisystem disorder caused by a defect in glycoprotein biosynthesis and characterized by under-glycosylated serum glycoproteins. Congenital disorders of glycosylation result in a wide variety of clinical features, such as defects in the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions.

    ID gène
    440138
    Pathways
    SARS-CoV-2 Protein Interactome
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