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CCL17 抗体 (AA 338-558)

This anti-CCL17 antibody is a 兔 多克隆 antibody detecting CCL17 in WB. Suitable for 人.
产品编号 ABIN1886379
发货至: 中国
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Quick Overview for CCL17 抗体 (AA 338-558) (ABIN1886379)

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)
  • 抗原表位

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    AA 338-558

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 338 and 558 of Human ABCD2
  • 应用备注

    Suggested dilutions:
    Western blotting: 1.500-1.3000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    储存液

    Thimerosal (Merthiolate)

    注意事项

    Biohazard Informations: This product contains thimerosal which is hazardous.

    储存条件

    4 °C/-20 °C

    储存方法

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • 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.[provided by RefSeq]

    分子量

    83 kDa

    基因ID

    225

    NCBI登录号

    NM_005164, NP_005155
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