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

HADH 抗体

This anti-HADH antibody is a 兔 多克隆 antibody detecting HADH in WB, IHC, ELISA 和 IP. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN5702281
发货至: 中国

Quick Overview for HADH 抗体 (ABIN5702281)

抗原

See all HADH 抗体
HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))

适用

  • 39
  • 36
  • 22
  • 8
  • 5
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
人, 小鼠, 大鼠

宿主

  • 39
  • 14
  • 1
  • 1

克隆类型

  • 42
  • 13
多克隆

标记

  • 26
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This HADH antibody is un-conjugated

应用范围

  • 40
  • 14
  • 13
  • 13
  • 13
  • 9
  • 9
  • 9
  • 6
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunoprecipitation (IP)
  • 原理

    HADH antibody

    免疫原

    hydroxyacyl-Coenzyme A dehydrogenase

    亚型

    IgG
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    说明

    HepG2 cells were subjected to SDS PAGE followed by western blot with FNab03747(HADH antibody) at dilution of 1:500

    限制

    仅限研究用
  • 缓冲液

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

    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.

    注意事项

    Avoid repeated freeze / thaw cycles.

    储存条件

    -20 °C

    储存方法

    -20°C for 12 months

    有效期

    12 months
  • 抗原

    HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))

    别名

    HADH

    背景

    Synonyms: Hydroxyacyl-coenzyme A dehydrogenase, mitochondrial (HCDH)|Medium and short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase|Short-chain 3-hydroxyacyl-CoA dehydrogenase|HADH|HAD|HAD1|HADHSC|SCHAD

    Background: This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene of this gene on chromosome 15.

    分子量

    34 kDa

    基因ID

    3033

    UniProt

    Q16836

    途径

    Negative Regulation of Hormone Secretion, Monocarboxylic Acid Catabolic Process
You are here:
Chat with us!