AGL anticorps (C-Term)
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- Antigène Voir toutes AGL Anticorps
- AGL (Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL))
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Épitope
- AA 1479-1510, C-Term
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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 AGL est non-conjugé
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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 1479-1510 amino acids from the C-terminal region of human AGL.
- Isotype
- Ig Fraction
- Top Product
- Discover our top product AGL Anticorps primaire
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- Indications d'application
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For WB starting dilution is: 1:1000
For IF starting dilution is: 1:10~50 - Restrictions
- For Research Use only
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- 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.
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- 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
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