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人々 SPG21 transcript variant 1 Gene ORF cDNA clone expression plasmid, N-HA タグ

データシートレビュー関連製品プロトコル
Human SPG21 cDNA クローン製品情報
Gene_bank_ref_id:NM_016630.3
cDNA サイズ:927bp
cDNA の説明:Full length Clone DNA of Homo sapiens spastic paraplegia 21 (autosomal recessive, Mast syndrome), transcript variant 1 with N terminal HA tag.
遺伝子の別名:MAST, ACP33, GL010, BM-019, MASPARDIN
:Human
ベクター:pCMV3-N-HA
Plasmid:
制限サイト:
タグ シーケンス:HA Tag Sequence: TATCCTTACGACGTGCCTGACTACGCC
シーケンスの説明:
Sequencing primers:T7(TAATACGACTCACTATAGGG) BGH(TAGAAGGCACAGTCGAGG)
Promoter:Enhanced CMV mammalian cell promoter
Application:Stable or Transient mammalian expression
Antibiotic in E.coli:Kanamycin
Antibiotic in mammalian cell:Hygromycin
Shipping_carrier:Each tube contains lyophilized plasmid.
保存:The lyophilized plasmid can be stored at room temperature for three months.
HA Tag Info

Human influenza hemagglutinin (HA) is a surface glycoprotein required for the infectivity of the human virus. The HA tag is derived from the HA-molecule corresponding to amino acids 98-106 has been extensively used as a general epitope tag in expression vectors. Many recombinant proteins have been engineered to express the HA tag, which does not appear to interfere with the bioactivity or the biodistribution of the recombinant protein. This tag facilitates the detection, isolation, and purification of the proteins.

The actual HA tag is as follows: 5' TAC CCA TAC GAT GTT CCA GAT TAC GCT 3' or 5' TAT CCA TAT GAT GTT CCA GAT TAT GCT 3' The amino acid sequence is: YPYDVPDYA.

人々 SPG21 transcript variant 1 Gene ORF cDNA clone expression plasmid, N-HA タグ on other vectors
人々 SPG21 transcript variant 1 Gene ORF cDNA clone expression plasmid, C-GFPSpark タグHG10522-ACGJPY54405
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人々 SPG21 transcript variant 1 Gene ORF cDNA clone expression plasmid, N-GFPSpark タグHG10522-ANGJPY54405
人々 SPG21 transcript variant 1 Gene ORF cDNA clone expression plasmid, N-OFPSpark タグHG10522-ANRJPY54405
人々 SPG21 transcript variant 1 Gene ORF cDNA clone expression plasmid, C-Flag タグHG10522-CFJPY47151
人々 SPG21 transcript variant 1 Gene ORF cDNA clone expression plasmid, C-His タグHG10522-CHJPY47151
人々 SPG21 transcript variant 1 Gene ORF cDNA clone expression plasmid, C-Myc タグHG10522-CMJPY47151
人々 SPG21 transcript variant 1 Gene ORF cDNA clone expression plasmid, C-HA タグHG10522-CYJPY47151
人々 SPG21 transcript variant 1 Gene ORF cDNA clone in cloning vectorHG10522-MJPY18135
人々 SPG21 transcript variant 1 Gene ORF cDNA clone expression plasmid, C-Flag タグHG10522-M-FJPY47151
人々 SPG21 transcript variant 1 Gene ORF cDNA clone expression plasmid, N-Flag タグHG10522-NFJPY47151
人々 SPG21 transcript variant 1 Gene ORF cDNA clone expression plasmid, N-His タグHG10522-NHJPY47151
人々 SPG21 transcript variant 1 Gene ORF cDNA clone expression plasmid, N-Myc タグHG10522-NMJPY47151
人々 SPG21 transcript variant 1 Gene ORF cDNA clone expression plasmid, N-HA タグHG10522-NYJPY47151
人々 SPG21 transcript variant 1 Gene ORF cDNA clone expression plasmidHG10522-UTJPY47151
 発現ベクターの詳細情報
Product nameProduct name
背景

Spastic paraplegia 21 (SPG21), also known as acid Cluster Protein 33 (ACP33) and Mast syndrome protein, is a member of the AB hydrolase superfamily. Human SPG21 is a 308 amino acid residue protein widely expressed in all tissues, including heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas. SPG21 binds to the hydrophobic C-terminal amino acids of CD4 which are involved in repression of T cell activation via the noncatalytic alpha/beta hydrolase fold domain. SPG21 thus is proposed to play a role as a negative regulatory factor in CD4-dependent T-cell activation of CD4. Defects in SPG21 are the cause of spastic paraplegia autosomal recessive type 21, also known as Mast syndrome, a neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Rate of progression and the severity of symptoms are quite variable. SPG21 is also associated with dementia and other central nervous system abnormalities.

参考文献
  • Zeitlmann L. et al., 2001, J Biol Chem. 276: 9123-32.
  • Simpson M. A. et al., 2003, Am J Hum Genet. 73: 1147-156.
  • Ota T. et al., 2004, Nat. Genet.36: 40-45.
  • Kedmi M. et al., 2007, Physiol Genomics. 28: 213-22.
  • Hanna M. C. et al., 2009, Neurogenetics.10: 217-28.
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