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Chemokine (C-C Motif) Ligand 17 (CCL17) (N-Term) Peptide

CCL17 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN8096850
发货至: 中国
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Quick Overview for Chemokine (C-C Motif) Ligand 17 (CCL17) (N-Term) Peptide (ABIN8096850)

抗原

CCL17 (Chemokine (C-C Motif) Ligand 17 (CCL17))

宿主

人

资源

  • 5
合成

应用范围

Blocking Peptide (BP), Western Blotting (WB)
  • 蛋白结构域

    N-Term

    原理

    ABCD2 Peptide - N-terminal region

    序列

    FIIKLIKWLM IAIPATFVNS AIRYLECKLA LAFRTRLVDH AYETYFTNQT
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    说明

    This is a synthetic peptide designed for use in combination with anti-ABCD2 Antibody(ARP43657_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications. Please inquire for more details.

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Add 100 µL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    缓冲液

    Lyophilized powder

    储存条件

    -20 °C

    储存方法

    For longer periods of storage, store at -20 °C. Avoid repeat freeze-thaw cycles.
  • 抗原

    CCL17 (Chemokine (C-C Motif) Ligand 17 (CCL17))

    背景

    Background Information: 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. The function of this peroxisomal membrane protein is unknown, however this protein is speculated to function as a dimerization partner of ABCD1 and/or other peroxisomal ABC transporters. Mutations in this gene have been observed in patients with adrenoleukodystrophy, a severe demyelinating disease. This gene has been identified as a candidate for a modifier gene, accounting for the extreme variation among adrenoleukodystrophy phenotypes. This gene is also a candidate for a complement group of Zellweger syndrome, a genetically heterogeneous disorder of peroxisomal biogenesis.

    Alternative Symbols: ABC39, ALDL1, ALDR, ALDRP, hALDR

    分子量

    83kDa

    基因ID

    225

    NCBI登录号

    NP_005155

    UniProt

    Q9UBJ2
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