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MAGEA2 抗体 (N-Term)

This anti-MAGEA2 antibody is a 兔 多克隆 antibody detecting MAGEA2 in WB 和 FACS. Suitable for 人.
产品编号 ABIN390106
发货至: 中国

Quick Overview for MAGEA2 抗体 (N-Term) (ABIN390106)

抗原

See all MAGEA2 抗体
MAGEA2 (Melanoma Antigen Family A, 2 (MAGEA2))

适用

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宿主

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克隆类型

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多克隆

标记

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This MAGEA2 antibody is un-conjugated

应用范围

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Western Blotting (WB), Flow Cytometry (FACS)

克隆位点

RB2194
  • 抗原表位

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    AA 81-108, N-Term

    纯化方法

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    免疫原

    This MAGEA2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 81-108 amino acids from the N-terminal region of human MAGEA2.

    亚型

    Ig Fraction
  • 应用备注

    WB: 1:2000. FC: 1:25

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    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

    4 °C,-20 °C

    储存方法

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    有效期

    6 months
  • 抗原

    MAGEA2 (Melanoma Antigen Family A, 2 (MAGEA2))

    别名

    MAGEA2

    背景

    MAGEA2 is a member of the MAGEA gene family. The members of this family have their entire coding sequences located in the last exon, and the encoded proteins show 50 to 80 % sequence identity between each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are expressed at a high level in a number of tumors of various histologic types, and are silent in normal tissues with the exception of testis and placenta. The MAGEA genes are clustered on chromosome Xq28. They may be implicated in some hereditary disorders, such as dyskeratosis congenita. This gene has two identical copies at different loci.

    基因ID

    4101

    NCBI登录号

    NP_005352, NP_705692, NP_786884, NP_786885

    UniProt

    P43356
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