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CCL17 抗体 (AA 553-582)

This anti-CCL17 antibody (ABIN5647610) is a Rabbit Polyclonal antibody detecting CCL17 in WB, ELISA, IHC, FACS. Suitable for Human.
产品编号 ABIN5647610
发货至: 中国

Quick Overview for CCL17 抗体 (AA 553-582) (ABIN5647610)

抗原

See all CCL17 抗体
CCL17 (Chemokine (C-C Motif) Ligand 17 (CCL17))

适用

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宿主

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克隆类型

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多克隆

标记

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This CCL17 antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS)
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    AA 553-582

    纯化方法

    Antigen affinity purified

    免疫原

    A portion of amino acids 553-582 from the human protein was used as the immunogen for this ABCD2 antibody.

    亚型

    Ig Fraction
  • 应用备注

    Western blot: 1:1000,IHC (Paraffin): 1:10-1:50,Flow Cytometry: 1:10-1:50

    限制

    仅限研究用
  • 缓冲液

    In 1X PBS, pH 7.4, with 0.09 % sodium azide

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Aliquot the ABCD2 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • 抗原

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

    别名

    ABCD2

    背景

    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.

    UniProt

    Q9UBJ2
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