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首页  >  酶联免疫试剂盒  >  Rat Slc33a1 ELISA Kit
Slc33a1 (基因名), Acetyl-coenzyme A transporter 1 (蛋白名), ACATN_RAT.
产品名称:

Rat Slc33a1/ Acetyl-coenzyme A transporter 1 ELISA Kit

货号:
-
商标:
EIAab®
监管等级:
别名:

AT-1, Solute carrier family 33 member 1, Acatn

检测方法:
ELISA
特异性:
Natural and recombinant rat Acetyl-coenzyme A transporter 1
样品类型:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
样品数据:
研究领域:
-
Rat Slc33a1 ELISA Kit
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Rat Slc33a1 ELISA Kit
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产品说明书


通用注释


亚单元:
N/A


功能:
Probable acetyl-CoA transporter necessary for O-acetylation of gangliosides. Negatively regulates BMP signaling.


亚细胞位置:
Endoplasmic reticulum membrane Multi-pass membrane protein


该产品尚未在任何出版物中被引用。

[1].
"A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42)."

[2].
"Expression cloning and characterization of a cDNA encoding a novel membrane protein required for the formation of O-acetylated ganglioside: a putative acetyl-CoA transporter."

[3].
"Identification and functional analysis of a SLC33A1: c.339T>G (p.Ser113Arg) variant in the original SPG42 family."

[4].
"Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin."

[5].
"A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42)."

[6].
"The acetyl-CoA transporter family SLC33."

[7].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[8].
"Architecture of the human interactome defines protein communities and disease networks."

[9].
"Increased expression of AT-1/SLC33A1 causes an autistic-like phenotype in mice by affecting dendritic branching and spine formation."

[10].
"A human interactome in three quantitative dimensions organized by stoichiometries and abundances."
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