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MYL3/CMLC1 抗体
MYL3
适用: 人, 小鼠, 大鼠
WB, ELISA, IF
宿主: 兔
Polyclonal
unconjugated
MYL3/CMLC1抗体详情
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抗原
See all MYL3/CMLC1 (MYL3) 抗体
MYL3/CMLC1 (MYL3)
(Myosin, Light Chain 3 (MYL3))
适用
All reactivities for MYL3/CMLC1 抗体
人, 小鼠, 大鼠
宿主
All hosts for MYL3/CMLC1 抗体
兔
克隆类型
All clonalities for MYL3/CMLC1 抗体
多克隆
标记
All conjugates for MYL3/CMLC1 抗体
This MYL3/CMLC1 antibody is un-conjugated
应用范围
All applications for MYL3/CMLC1 抗体
Western Blotting (WB), ELISA, Immunofluorescence (IF)
纯化方法
Immunogen affinity purified
纯度
≥95 % as determined by SDS-PAGE
免疫原
MYL3
亚型
IgG
Top Product
Discover our top product MYL3 Primary Antibody
Alternatives
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使用细节
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应用备注
WB: 1:500 - 1:2000, IF: 1:50 - 1:200
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 and 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
-20°C for 12 months (Avoid repeated freeze / thaw cycles.)
有效期
12 months
MYL3/CMLC1目标详情
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抗原
MYL3/CMLC1 (MYL3)
(Myosin, Light Chain 3 (MYL3))
别名
MYL3 (MYL3 产品 )
别名
CMD1S antibody, CMH1 antibody, MPD1 antibody, MYHCB antibody, SPMD antibody, SPMM antibody, B-MHC antibody, MyHC-I antibody, Myhc-b antibody, Myhcb antibody, beta-MHC antibody, MLC1s antibody, MLC1v antibody, Mylc antibody, VLC1 antibody, Mylc1v antibody, CMH8 antibody, MLC1SB antibody, MLC1V antibody, mlc1v antibody, myl3-a antibody, myl3-b antibody, myl3.L antibody, zgc:103441 antibody, myosin heavy chain 7 antibody, myosin, heavy polypeptide 7, cardiac muscle, beta antibody, myosin, light polypeptide 3 antibody, myosin light chain 3 antibody, myosin light chain 3 S homeolog antibody, cardiac myosin light chain-1 antibody, MYH7 antibody, Myh7 antibody, Myl3 antibody, MYL3 antibody, myl3.S antibody, cmlc1 antibody
背景
Synonyms:CMH8, MLC-lV/sb, MLC1SB, MLC1V, VLC1, VLCl Background:MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy.
分子量
23 kDa
基因ID
4634
UniProt
P08590
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