电话:
+86 (0512) 65829739
传真:
+86 (010) 6788 5057
电子邮件:
orders@antibodies-online.cn

Phenylalanine Hydroxylase 抗体

This anti-Phenylalanine Hydroxylase antibody is a 兔 多克隆 antibody detecting Phenylalanine Hydroxylase in WB, ICC 和 IF. Suitable for 人.
产品编号 ABIN7467130
发货至: 中国

Quick Overview for Phenylalanine Hydroxylase 抗体 (ABIN7467130)

抗原

See all Phenylalanine Hydroxylase 抗体
Phenylalanine Hydroxylase

适用

  • 66
  • 26
  • 17

宿主

  • 52
  • 15
  • 1

克隆类型

  • 52
  • 16
多克隆

标记

  • 44
  • 9
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Phenylalanine Hydroxylase antibody is un-conjugated

应用范围

  • 55
  • 34
  • 25
  • 17
  • 14
  • 8
  • 5
  • 3
  • 2
  • 1
Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)
  • 交叉反应

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the center region of human PAH. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Validation: Orthogonal

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1.76 mg/mL

    缓冲液

    1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300

    储存液

    ProClin

    注意事项

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

    储存条件

    4 °C,-20 °C

    储存方法

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    Phenylalanine Hydroxylase

    背景

    Phenylalanine hydroxylase , PH , PKU , PKU1,This gene encodes a member of the biopterin-dependent aromatic amino acid hydroxylase protein family. The encoded phenylalanine hydroxylase enzyme hydroxylates phenylalanine to tyrosine and is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria. [provided by RefSeq, Aug 2017]

    分子量

    52 kDa

    基因ID

    5053

    UniProt

    P00439
You are here:
Chat with us!