MYL3 purified MaxPab rabbit polyclonal antibody (D01P)-抗体-抗体-生物在线
亚诺法生技股份有限公司(Abnova)
MYL3 purified MaxPab rabbit polyclonal antibody (D01P)

MYL3 purified MaxPab rabbit polyclonal antibody (D01P)

商家询价

产品名称: MYL3 purified MaxPab rabbit polyclonal antibody (D01P)

英文名称: MYL3 purified MaxPab rabbit polyclonal antibody (D01P)

产品编号: H00004634-D01P

产品价格: null

产品产地: 台湾

品牌商标: Abnova

更新时间: null

使用范围:

亚诺法生技股份有限公司(Abnova)
  • 联系人 :
  • 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
  • 邮编 : 11493
  • 所在区域 : 台湾
  • 电话 : +886-920**1152 点击查看
  • 传真 : 点击查看
  • 邮箱 : sales@abnova.com.tw

  • Specification
  • Product Description:
  • Rabbit polyclonal antibody raised against a full-length human MYL3 protein.
  • Immunogen:
  • MYL3 (NP_000249.1, 1 a.a. ~ 195 a.a) full-length human protein.
  • Sequence:
  • MAPKKPEPKKDDAKAAPKAAPAPAPPPEPERPKEVEFDASKIKIEFTPEQIEEFKEAFMLFDRTPKCEMKITYGQCGDVLRALGQNPTQAEVLRVLGKPRQEELNTKMMDFETFLPMLQHISKNKDTGTYEDFVEGLRVFDKEGNGTVMGAELRHVLATLGERLTEDEVEKLMAGQEDSNGCINYEAFVKHIMSS
  • Host:
  • Rabbit
  • Reactivity:
  • Human
  • Storage Buffer:
  • In 1x PBS, pH 7.2
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Quality Control Testing:
  • Antibody reactive against mammalian transfected lysate.
  • Applications
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • Western Blot analysis of MYL3 expression in transfected 293T cell line (H00004634-T02) by MYL3 MaxPab polyclonal antibody.

    Lane 1: MYL3 transfected lysate(21.90 KDa).
    Lane 2: Non-transfected lysate.
  • Protocol Download
  • Detection Antibody
  • Application Image
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • enlarge
  • Detection Antibody
  • Gene Information
  • Entrez GeneID:
  • 4634
  • Gene Name:
  • MYL3
  • Gene Alias:
  • CMH8,MLC1SB,MLC1V,VLC1
  • Gene Description:
  • myosin, light chain 3, alkali; ventricular, skeletal, slow
  • Gene Summary:
  • 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. [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000165922,myosin, light polypeptide 3, alkali; ventricular, skeletal, slow,slow skeletal ventricular myosin alkali light chain 3

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