人 MAPK8 (NM_002750) cDNA克隆

Accession: NM_002750
基因名称: MAPK8
基因别名: JNK; JNK1; PRKM8; SAPK1; JNK-46; JNK1A2; SAPK1c; JNK21B1/2
基因描述: Homo sapiens mitogen-activated protein kinase 8 (MAPK8), transcript variant JNK1-a1, mRNA.
种属: Human
CDS区长度: 1155 (查看编码区序列)
翻译后氨基酸长度: 384 (查看氨基酸序列)
Transcript Variant: This variant (JNK1-a1) uses a different acceptor splice site in the last coding exon compared to transcript variant JNK1-a2, resulting in a frameshift and a shorter isoform (JNK1 alpha1) with a different C-terminus, compared to isoform JNK1 alpha2. The JNK1-a1 variant differs from the JNK1-b1 variant in the use of an alternate internal coding exon of the same length. Thus, JNK1 alpha1 isoform is the same length as JNK1 beta1 isoform, with a few aa difference in an internal protein segment.
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G122145 人 MAPK8 (NM_002750) cDNA克隆 pDONR223 2ug质粒 点击询价
人 MAPK8 (NM_001278548) cDNA克隆 transcript variant 5
人 MAPK8 (NM_002750) cDNA克隆 transcript variant JNK1-a1
人 MAPK8 (NM_139049) cDNA克隆 transcript variant JNK1-a2
人 MAPK8 (NM_139046) cDNA克隆 transcript variant JNK1-b1
人 MAPK8 (NM_139047) cDNA克隆 transcript variant JNK1-b2
人 MAPK8 (NM_001278547) cDNA克隆 transcript variant JNK1-b2

The protein encoded by this gene is a member of the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. This kinase is activated by various cell stimuli, and targets specific transcription factors, and thus mediates immediate-early gene expression in response to cell stimuli. The activation of this kinase by tumor-necrosis factor alpha (TNF-alpha) is found to be required for TNF-alpha induced apoptosis. This kinase is also involved in UV radiation induced apoptosis, which is thought to be related to cytochrom c-mediated cell death pathway. Studies of the mouse counterpart of this gene suggested that this kinase play a key role in T cell proliferation, apoptosis and differentiation. Five alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jun 2013]