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COG8 抗体 (N-Term)

The 兔 多克隆 anti-COG8 antibody is suitable to detect COG8 in samples from 人. It has been validated for WB.
产品编号 ABIN5517541
发货至: 中国
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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 COG8 抗体 (N-Term) (ABIN5517541)

抗原

See all COG8 抗体
COG8 (Component of Oligomeric Golgi Complex 8 (COG8))

适用

  • 10
  • 2
  • 1
人

宿主

  • 7
  • 2
  • 1
兔

克隆类型

  • 10
多克隆

标记

  • 7
  • 1
  • 1
  • 1
This COG8 antibody is un-conjugated

应用范围

  • 5
  • 5
  • 2
  • 1
  • 1
Western Blotting (WB)
  • 抗原表位

    • 4
    • 2
    • 1
    N-Term

    原理

    COG8 Antibody - N-terminal region

    序列

    MATAATIPSV ATATAAALGE VEDEGLLASL FRDRFPEAQW RERPDVGRYL

    纯化方法

    Affinity purified

    免疫原

    The immunogen is a synthetic peptide directed towards the N terminal region of human COG8
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    说明

    We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP78473-100UG

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.5 mg/mL

    缓冲液

    Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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

    prevent freeze-thaw cycles

    储存条件

    4 °C,-20 °C

    储存方法

    For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
  • 抗原

    COG8 (Component of Oligomeric Golgi Complex 8 (COG8))

    别名

    COG8

    背景

    Background Information: This gene encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance.

    Gene Name: component of oligomeric golgi complex 8

    Alternative Symbols: DOR1, CDG2H

    Protein Name: conserved oligomeric Golgi complex subunit 8

    分子量

    68 kDa

    基因ID

    84342

    NCBI登录号

    NP_115758

    UniProt

    Q96MW5
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