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AGL 抗体 (AA 1233-1532)
AGL
适用: 人
WB
宿主: 兔
Polyclonal
unconjugated
AGL抗体详情
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抗原
See all AGL 抗体
AGL
(Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL))
抗原表位
All epitopes for AGL 抗体
AA 1233-1532
适用
All reactivities for AGL 抗体
人
宿主
All hosts for AGL 抗体
兔
克隆类型
All clonalities for AGL 抗体
多克隆
标记
All conjugates for AGL 抗体
This AGL antibody is un-conjugated
应用范围
All applications for AGL 抗体
Western Blotting (WB)
序列
EGFNITAGVD EETGFVYGGN RFNCGTWMDK MGESDRARNR GIPATPRDGS AVEIVGLSKS AVRWLLELSK KNIFPYHEVT VKRHGKAIKV SYDEWNRKIQ DNFEKLFHVS EDPSDLNEKH PNLVHKRGIY KDSYGASSPW CDYQLRPNFT IAMVVAPELF TTEKAWKALE IAEKKLLGPL GMKTLDPDDM VYCGIYDNAL DNDNYNLAKG FNYHQGPEWL WPIGYFLRAK LYFSRLMGPE TTAKTIVLVK NVLSRHYVHL ERSPWKGLPE LTNENAQYCP FSCETQAWSI ATILETLYDL
交叉反应
人, 小鼠
产品特性
Polyclonal Antibodies
纯化方法
Affinity purification
免疫原
Recombinant fusion protein containing a sequence corresponding to amino acids 1233-1532 of human AGL (NP_000633.2).
亚型
IgG
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Discover our top product AGL Primary Antibody
Alternatives
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使用细节
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应用备注
WB,1:500 - 1:2000
限制
仅限研究用
贮存及处理
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状态
Liquid
缓冲液
PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
储存液
Sodium azide
注意事项
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
储存条件
-20 °C
储存方法
Store at -20°C. Avoid freeze / thaw cycles.
AGL目标详情
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抗原
AGL
(Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL))
别名
AGL (AGL 产品 )
别名
DDBDRAFT_0219237 antibody, DDBDRAFT_0234114 antibody, DDB_0219237 antibody, DDB_0234114 antibody, GDE antibody, 1110061O17Rik antibody, 9430004C13Rik antibody, 9630046L06Rik antibody, AI850929 antibody, C77197 antibody, amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase antibody, glycogen debranching enzyme antibody, glycogen debranching protein antibody, amylo-1,6-glucosidase, 4-alpha-glucanotransferase antibody, AGL antibody, agl antibody, MMAH_RS03870 antibody, Agl antibody
背景
This gene encodes the 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 this 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. Alternatively spliced transcripts encoding different isoforms have been described.,AGL,GDE,Cancer,Signal Transduction,Endocrine & Metabolism,Carbohydrate metabolism,AGL
分子量
172 kDa/174 kDa
基因ID
178
UniProt
P35573
途径
Cellular Glucan Metabolic Process
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