TPM1 cDNA ORF Clone, Mouse, C-HA tag

Cat: MG52560-CY

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TPM1 cDNA ORF Clone, Mouse, C-HA tag 基本信息

基因

种属
Mouse
NCBI 参考序列号
参考序列ORF长度
846 bp
描述
Full length Clone DNA of Mouse ancient ubiquitous protein 1 with C terminal HA tag.

质粒

启动子
Enhanced CMV promoter
载体
标签序列
HA Tag Sequence: TATCCTTACGACGTGCCTGACTACGCC
测序引物
T7( 5' TAATACGACTCACTATAGGG 3' )
BGH( 5' TAGAAGGCACAGTCGAGG 3' )
质控
The plasmid is confirmed by full-length sequencing.

筛选

抗生素(大肠杆菌)
Kanamycin
抗生素(哺乳动物细胞)
Hygromycin
应用
Stable or Transient mammalian expression

储存 & 运输

运输
Each tube contains lyophilized plasmid.
储存
The lyophilized plasmid can be stored at ambient temperature for three months.

**Sino Biological guarantees 100% sequence accuracy of all synthetic DNA constructs we deliver, but we do not guarantee protein expression in your experimental system. Protein expression is influenced by many factors that may vary between experiments or laboratories.**

TPM1 cDNA ORF Clone, Mouse, C-HA tag Alternative Names

AA986836 cDNA ORF Clone, Mouse;AI854628 cDNA ORF Clone, Mouse;alpha-TM cDNA ORF Clone, Mouse;TM2 cDNA ORF Clone, Mouse;Tm3 cDNA ORF Clone, Mouse;Tmpa cDNA ORF Clone, Mouse;Tpm-1 cDNA ORF Clone, Mouse

TPM1 Background Information

TPM1, also known as tropomyosin-1, is a member of the tropomyosin family. Members of this family are highly conserved, widely distributed actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. highly conserved, widely distributed actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. TPM1 is one type of alpha helical chain that forms the predominant tropomyosin of striated muscle. It binds to actin filaments in muscle and non-muscle cells. TPM1 plays a central role, in association with the troponin complex, in the calcium dependent regulation of vertebrate striated muscle contraction.

Full Name
tropomyosin 1 (alpha)
References
  • Mogensen J. et al., 1999, Cytogenet Cell Genet. 84 (1-2): 35-6.
  • Brown H R. et al., 1985, Proc Natl Acad Sci. 82 (8): 2359-63.
  • Lees-Miller JP. et al., 1992, BioEssays. 13 (9): 429-37.
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