AGL anticorps (AA 357-387)

N° du produit ABIN5535955

Détail du produit anti-AGL anticorps

Antigène: AGL (Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL))

Épitope: AA 357-387

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AGL est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF)

Purification: This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis

Immunogène: This AGL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 357-387 amino acids from the Central region of human AGL.

Isotype: Ig Fraction

Information d'application

Indications d'application: For WB starting dilution is: 1:1000

For IF starting dilution is: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 2 mg/mL

Buffer: 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: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Détails sur AGL

Antigène: AGL (Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL))

Autre désignation: AGL (AGL Produits)

Synonymes: anticorps DDBDRAFT_0219237, anticorps DDBDRAFT_0234114, anticorps DDB_0219237, anticorps DDB_0234114, anticorps GDE, anticorps 1110061O17Rik, anticorps 9430004C13Rik, anticorps 9630046L06Rik, anticorps AI850929, anticorps C77197, anticorps amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase, anticorps glycogen debranching enzyme, anticorps glycogen debranching protein, anticorps amylo-1,6-glucosidase, 4-alpha-glucanotransferase, anticorps AGL, anticorps agl, anticorps MMAH_RS03870, anticorps Agl

Sujet: AGL is a glycogen debrancher enzyme which is involved in glycogen degradation. This enzyme has two independent catalytic activities which occur at different sites on the protein: a 4-alpha-glucotransferase activity and a amylo-1,6-glucosidase activity. Mutations in the AGL gene are associated with glycogen storage disease although a wide range of enzymatic and clinical variability occurs which may be due to tissue-specific alternative splicing.

Poids moléculaire: 175 kDa

ID gène: 178

UniProt: P35573

Pathways: Cellular Glucan Metabolic Process