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

HMBS 抗体

The 兔 单克隆 anti-HMBS antibody is suitable to detect HMBS in samples from 人. It has been validated for WB.
产品编号 ABIN7881138
发货至: 中国
Contact our Customer Service for availability and price in your country. Contact Info

Our Local Distributor

中国
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for HMBS 抗体 (ABIN7881138)

抗原

See all HMBS 抗体
HMBS (Hydroxymethylbilane Synthase (HMBS))

适用

  • 67
  • 36
  • 36
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1

宿主

  • 61
  • 5
  • 1

克隆类型

  • 51
  • 16
单克隆

标记

  • 32
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This HMBS antibody is un-conjugated

应用范围

  • 44
  • 13
  • 13
  • 9
  • 7
  • 5
  • 5
  • 4
  • 4
  • 1
  • 1
  • 1
Western Blotting (WB)

克隆位点

FEG-8
  • 原理

    HMBS Antibody / Hydroxymethylbilane synthase

    纯化方法

    Affinity purified

    免疫原

    A synthetic peptide specific to human HMBS was used as the immunogen for the HMBS antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the HMBS antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Antibody in PBS with 0.02 % sodium azide, 50 % glycerol and 0.4-0.5 mg/mL BSA

    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

    Store the HMBS antibody at -20oC.
  • 抗原

    HMBS (Hydroxymethylbilane Synthase (HMBS))

    别名

    HMBS

    背景

    The HMBS gene encodes a member of the hydroxymethylbilane synthase superfamily. The encoded protein is the third enzyme of the heme biosynthetic pathway and catalyzes the head to tail condensation of four porphobilinogen molecules into the linear hydroxymethylbilane. Mutations in this gene are associated with the autosomal dominant disease acute intermittent porphyria. [RefSeq]

    UniProt

    P08397
You are here: