本公司所有产品仅供科研使用,不用于人体及临床诊断。
027-59234612(+86)
我的积分
注册  /  登录
EIAab
首页  >  酶联免疫试剂盒  >  Human ABCD4 ELISA Kit
ABCD4 (基因名), ATP-binding cassette sub-family D member 4 (蛋白名), ABCD4_HUMAN.
产品名称:

Human ABCD4/ ATP-binding cassette sub-family D member 4 ELISA Kit

货号:
-
商标:
EIAab®
监管等级:
别名:

PMP70-related protein, P70R, Peroxisomal membrane protein 1-like, PXMP1-L, Peroxisomal membrane protein 69, PMP69, PXMP1L

检测方法:
ELISA
特异性:
Natural and recombinant human ATP-binding cassette sub-family D member 4
样品类型:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
样品数据:
研究领域:
-
Human ABCD4 ELISA Kit
规格 & 价格: 登录.
×
Human ABCD4 ELISA Kit
邮箱 *
消息 *
Please 登录.
产品说明书


通用注释


亚单元:
Homodimer or heterodimer.


功能:
May be involved in intracellular processing of vitamin B12 (cobalamin). Could play a role in the lysosomal release of vitamin B12 into the cytoplasm.


亚细胞位置:
Peroxisome membrane Multi-pass membrane protein


该产品尚未在任何出版物中被引用。

[1].
"Primary structure of human PMP69, a putative peroxisomal ABC-transporter."

[2].
"Genomic organization and chromosomal localization of the human peroxisomal membrane protein-1-like protein (PXMP1-L) gene encoding a peroxisomal ABC transporter."

[3].
"Identification of a fourth half ABC transporter in the human peroxisomal membrane."

[4].
"Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism."

[5].
"Association study between single-nucleotide polymorphisms in 199 drug-related genes and commonly measured quantitative traits of 752 healthy Japanese subjects."

[6].
"Decreased expression of ABCD4 and BG1 genes early in the pathogenesis of X-linked adrenoleukodystrophy."

[7].
"Targeting of the human adrenoleukodystrophy protein to the peroxisomal membrane by an internal region containing a highly conserved motif."

[8].
"Catalog of 605 single-nucleotide polymorphisms (SNPs) among 13 genes encoding human ATP-binding cassette transporters: ABCA4, ABCA7, ABCA8, ABCD1, ABCD3, ABCD4, ABCE1, ABCF1, ABCG1, ABCG2, ABCG4, ABCG5, and ABCG8."

[9].
"Architecture of the human interactome defines protein communities and disease networks."

[10].
"Clinical or ATPase domain mutations in ABCD4 disrupt the interaction between the vitamin B12-trafficking proteins ABCD4 and LMBD1."
关闭
Sample Data
关闭
Sample Data
关闭
Sample Data
用户中心 close
购物车 close
我的收藏 close
我的足迹 close
清除
产品对比 close
用户中心
购物车
我的收藏
我的足迹
产品对比
回到顶部
消息
close_message
产品名称 *
邮箱 *
消息 *
通知
new 留 言
规格 数量 价格 ($) 小计 1 ($)
小计 2: $
triangle
规格 数量 价格 ($)
你想做我们的代理并得到更低的折扣吗?
请联系我们:
电话:027-59234612(+86)
传真:027-59759960(+86)
邮箱:sales@eiaab.com