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SGCD 抗体
SGCD
适用: 人, 小鼠, 大鼠
IF
宿主: 兔
Polyclonal
unconjugated
SGCD抗体详情
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抗原
See all SGCD 抗体
SGCD
(Sarcoglycan, delta (35kDa Dystrophin-Associated Glycoprotein) (SGCD))
适用
All reactivities for SGCD 抗体
人, 小鼠, 大鼠
宿主
All hosts for SGCD 抗体
兔
克隆类型
All clonalities for SGCD 抗体
多克隆
标记
All conjugates for SGCD 抗体
This SGCD antibody is un-conjugated
应用范围
All applications for SGCD 抗体
Immunofluorescence (IF)
产品特性
Polyclonal Antibody
纯化方法
Affinity purification
免疫原
Recombinant fusion protein of human SGCD (NP_000328.2).
亚型
IgG
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Discover our top product SGCD Primary Antibody
Alternatives
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anti-Sarcoglycan, delta (35kDa Dystrophin-Associated Glycoprotein) (SGCD) (AA 37-86) antibody
SGCD
适用: 人, 小鼠, 大鼠, Cow, 兔, 豚鼠, Pig, Bat, Hamster, 猴
WB
宿主: 兔
Polyclonal
unconjugated
使用细节
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应用备注
IF 1:50-1:200
限制
仅限研究用
贮存及处理
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状态
Liquid
浓度
1 mg/mL
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.
SGCD目标详情
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抗原
SGCD
(Sarcoglycan, delta (35kDa Dystrophin-Associated Glycoprotein) (SGCD))
别名
SGCD (SGCD 产品 )
别名
BEST:GH21860 antibody, CG14808 antibody, CT34621 antibody, DmSCG-gammadelta antibody, Dmel\\CG14808 antibody, EG:4F1.1 antibody, GH21860 antibody, Sgcd antibody, wu:fc49e11 antibody, zgc:110649 antibody, 35DAG antibody, CMD1L antibody, DAGD antibody, SG-delta antibody, SGCDP antibody, SGD antibody, Delta-SG antibody, 35kDa antibody, delta-SG antibody, sarcoglycan delta antibody, Sarcoglycan delta antibody, sarcoglycan, delta (dystrophin-associated glycoprotein) antibody, sarcoglycan, delta antibody, SGCD antibody, Scgdelta antibody, sgcd antibody, Sgcd antibody
背景
The protein encoded by this gene is one of the four known components of the sarcoglycan complex, which is a subcomplex of the dystrophin-glycoprotein complex (DGC). DGC forms a link between the F-actin cytoskeleton and the extracellular matrix. This protein is expressed most abundantly in skeletal and cardiac muscle. Mutations in this gene have been associated with autosomal recessive limb-girdle muscular dystrophy and dilated cardiomyopathy. Alternatively spliced transcript variants encoding distinct isoforms have been observed for this gene.
基因ID
6444
UniProt
Q92629
途径
Maintenance of Protein Location
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