anti-ATP-Binding Cassette, Sub-Family D (Ald), Member 1 (ABCD1) 抗体产品概述

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anti-ATP-Binding Cassette, Sub-Family D (Ald), Member 1 抗体 (ABCD1)
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别名:
ABC42, ABCD1, Ald, Aldgh, ALDP, AMN, F2G19.18, F2G19_18, RGD1562128, WPP domain protein 2, zgc:172102
列出全部抗体 基因 基因ID UniProt
ABCD1 215 P33897
ABCD1 11666 P48410
ABCD1 363516  

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引用最多的anti-ATP-Binding Cassette, Sub-Family D (Ald), Member 1 抗体

  1. Human Polyclonal ABCD1 Primary Antibody for EIA, IHC (p) - ABIN950202 : Xie, Ke, Wang, Huang, Lan: [A novel missense mutation resulting in X-linked adrenoleukodystrophy in female heterozygotes of a Chinese family]. in Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2010 (PubMed)
    Show all 3 references for 950202

  2. Arabidopsis thaliana Polyclonal ABCD1 Primary Antibody for WB - ABIN334558 : Sun, Suen, Zhang, Liang, Carrie, Whelan, Ward, Hawkins, Jiang, Lim: A dual-targeted purple acid phosphatase in Arabidopsis thaliana moderates carbon metabolism and its overexpression leads to faster plant growth and higher seed yield. in The New phytologist 2012 (PubMed)
    Show all 2 references for 334558

更多抗ATP-Binding Cassette, Sub-Family D (Ald), Member 1的相互作用对抗体

Human ATP-Binding Cassette, Sub-Family D (Ald), Member 1 (ABCD1) interaction partners

  1. ABCD1 and ABCD2 (显示 Abcd2 抗体) are involved in the transport of long and very long chain fatty acids (VLCFA) or their CoA-derivatives into peroxisomes with different substrate specificities, while ABCD3 (显示 ABCD3 抗体) is involved in the transport of branched chain acyl-CoA (显示 GNPAT 抗体) into peroxisomes.ABCD4 is deduced to take part in the transport of vitamin B12 (显示 NDUFB3 抗体) from lysosomes into the cytosol.

  2. This study showed that the mutations of were detected in SPG11 (显示 SPG11 抗体), ATL1 (显示 ATL1 抗体), NIPA1 (显示 NIPA1 抗体), and ABCD1 in patient with hereditary spastic paraplegia.

  3. CCALD is the most common phenotype (64%) in our Chinese patients with X-ALD. Eight novel mutations in the ABCD1 gene identified are disease-causing mutations.

  4. The current study demonstrates that a single splicing mutation affects the ABCD1 transcripts and the ALDP protein function.

  5. both BCAP31 (显示 BCAP31 抗体) and ABCD1 were associated with hepatic cholestasis and death before 1 year. Remarkably, a patient with an isolated deletion at the 3'-end of SLC6A8 (显示 SLC6A8 抗体) had a similar severe phenotype as seen in BCAP31 (显示 BCAP31 抗体) deficiency

  6. Exome sequencing in two brothers with distinct phenotype including congenital language disorder, growth retardation, intellectual disability and urinary and fecal incontinence, identifies missense mutations in ABCD1 and DACH2 (显示 DACH2 抗体).

  7. As a result of loss of ABCD1, there is pathogenic accumulation of very long chain fatty acids which leads to mitochondrial dysfunction.

  8. We detected the same mutation of the ABCD1 gene in two unrelated patients with X-linked adrenoleukodystrophy.

  9. We describe four unrelated women with a late-onset progressive spastic paraparesis and heterozygous mutations in the ABCD1 gene

  10. X-inactivation pattern of the ABCD1 gene is associated with symptomatic status in female X-linked adrenoleukodystrophy carriers.

Mouse (Murine) ATP-Binding Cassette, Sub-Family D (Ald), Member 1 (ABCD1) interaction partners

  1. ABCD1 and its homolog ABCD2 (显示 Abcd2 抗体) exist mainly as homotetramers in the peroxisomal membrane

  2. during the active myelination phase the microsomal fatty acid elongation activity is stimulated in abcd1-deficient mice

  3. Deletion of AMPKalpha1 (显示 PRKAA1 抗体) in the mixed glial cells of Abcd1-KO mice induced spontaneous mitochondrial dysfunction

  4. Abcd2 (显示 Abcd2 抗体) is a strong modifier of the metabolic impairments in peritoneal macrophages of ABCD1-deficient mice

  5. Data indicate that astrocytes from adrenoleukodystrophy protein Abcd1-/- mice respond sensitively to long-term very-long-chain fatty acids (VLCFA) treatment.

  6. Our data support a link between oxidative stress and the deficiency of Abcd1 or Acox1 (显示 ACOX1 抗体) peroxisomal proteins.

  7. Study demonstrates that oxidative damage to proteins specifically affects five key enzymes of glycolysis and TCA (Tricarboxylic acid) cycle in spinal cords of Abcd1(-) mice.

  8. ALDP facilitates the interaction between peroxisomes and mitochondria, resulting, when ALDP is deficient in X-ALD, in increased VLCFA accumulation

  9. Accumulation of very long-chain fatty acids does not affect mitochindrial function in Abcd1 protein deficiency.

  10. Abcd1 and Abcd2 (显示 Abcd2 抗体) gene silencing sensitizes astrocytes for inflammation and may have a role in X-adrenoleukodystrophy

ATP-Binding Cassette, Sub-Family D (Ald), Member 1 (ABCD1) 抗原简介

Antigen Summary

The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. This peroxisomal membrane protein is likely involved in the peroxisomal transport or catabolism of very long chain fatty acids. Defects in this gene have been identified as the underlying cause of adrenoleukodystrophy, an X-chromosome recessively inherited demyelinating disorder of the nervous system.

Alternative names and synonyms associated with ATP-Binding Cassette, Sub-Family D (Ald), Member 1 (ABCD1)

  • ATP-binding cassette, sub-family D (ALD), member 1 (abcd1) 抗体
  • ATP-binding cassette, sub-family D (ALD), member 1 (ABCD1) 抗体
  • ATP-binding cassette sub-family D member 1 (CpipJ_CPIJ013253) 抗体
  • ATP-binding cassette sub-family D member 1 (VDBG_05717) 抗体
  • ATP-binding cassette sub-family D member 1 (ABCD1) 抗体
  • ATP-binding cassette, sub-family D (ALD), member 1 (Abcd1) 抗体
  • ATP-binding cassette, subfamily D (ALD), member 1 (Abcd1) 抗体
  • WPP domain-containing protein 2 (WPP2) 抗体
  • ABC42 抗体
  • ABCD1 抗体
  • Ald 抗体
  • Aldgh 抗体
  • ALDP 抗体
  • AMN 抗体
  • F2G19.18 抗体
  • F2G19_18 抗体
  • RGD1562128 抗体
  • WPP domain protein 2 抗体
  • zgc:172102 抗体

Protein level used designations for ABCD1

ATP-binding cassette, sub-family D (ALD), member 1 , adrenoleukodystrophy protein , ATP-binding cassette sub-family D member 1 , ATP-binding cassette sub-family D member 1-like , ATP-binding cassette, sub-family D, member 1 , X-linked adrenoleukodystrophy (ALD) gene homolog

GENE ID SPECIES
495468 Xenopus laevis
515178 Bos taurus
566367 Danio rerio
612520 Canis lupus familiaris
696794 Macaca mulatta
6046470 Culex quinquefasciatus
9531595 Verticillium alfalfae VaMs.102
100328741 Oryctolagus cuniculus
100493545 Xenopus (Silurana) tropicalis
100519529 Sus scrofa
100027916 Monodelphis domestica
100586126 Nomascus leucogenys
215 Homo sapiens
11666 Mus musculus
363516 Rattus norvegicus
841123 Arabidopsis thaliana
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