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CLN8 产品

(Ceroid-Lipofuscinosis, Neuronal 8 (Epilepsy, Progressive with Mental Retardation) (CLN8))

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This gene encodes a transmembrane protein belonging to a family of proteins containing TLC domains, which are postulated to function in lipid synthesis, transport, or sensing. The protein localizes to the endoplasmic reticulum (ER), and may recycle between the ER and ER-Golgi intermediate compartment. Mutations in this gene are associated with progressive epilepsy with mental retardation (EMPR), which is a subtype of neuronal ceroid lipofuscinoses (NCL). Patients with mutations in this gene have altered levels of sphingolipid and phospholipids in the brain. [provided by RefSeq, Jul 2008].

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Featured CLN8 Categories

CLN8 抗体

High quality antibodies with extensive validation data.

Recommended CLN8 抗体

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Reactivity
Application
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Cat. No.
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Datasheet
Reactivity Human
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Cat. No. ABIN7266285
Quantity 100 μL
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Reactivity Human, Rat
Application WB, ELISA, IF (cc), IF (p), IHC (fro), IHC (p), ICC
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Cat. No. ABIN1387794
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Reactivity Human
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Cat. No. ABIN7165205
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Recommended CLN8 蛋白

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Cat. No. ABIN3107938
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Reactivity Mouse
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Synonyms and alternative names related to CLN8

CLN8, transmembrane ER and ERGIC protein (CLN8), ceroid-lipofuscinosis, neuronal 8 (Cln8), CLN8, transmembrane ER and ERGIC protein (Cln8), C8orf61, EPMR, mnd

Protein level used designations for CLN8

  • ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
  • protein CLN8
  • motor neuron degeneration
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