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

CRYM 抗体

This anti-CRYM antibody is a 兔 多克隆 antibody detecting CRYM in ELISA 和 IHC. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN7247741
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 CRYM 抗体 (ABIN7247741)

抗原

See all CRYM 抗体
CRYM (Crystallin, mu (CRYM))

适用

  • 25
  • 10
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 24
  • 7

克隆类型

  • 25
  • 6
多克隆

标记

  • 22
  • 3
  • 2
  • 2
  • 1
  • 1
This CRYM antibody is un-conjugated

应用范围

  • 25
  • 14
  • 8
  • 5
  • 3
  • 2
  • 2
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • 产品特性

    Polyclonal Antibody

    纯化方法

    Antigen affinity purification

    免疫原

    Fusion protein of human CRYM

    亚型

    IgG
  • 应用备注

    IHC 1:50-1:200, ELISA 1:5000-1:10000

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1.14 mg/mL

    缓冲液

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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 at -20°C. Avoid freeze / thaw cycles.
  • 抗原

    CRYM (Crystallin, mu (CRYM))

    别名

    CRYM

    背景

    Crystallins are separated into two classes: taxon-specific and ubiquitous. The former class is also called phylogenetically-restricted crystallins. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. This gene encodes a taxon-specific crystallin protein that binds NADPH and has sequence similarity to bacterial ornithine cyclodeaminases. The encoded protein does not perform a structural role in lens tissue, and instead it binds thyroid hormone for possible regulatory or developmental roles. Mutations in this gene have been associated with autosomal dominant non-syndromic deafness.

    UniProt

    Q14894

    途径

    Hormone Transport, Sensory Perception of Sound
You are here: