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SYAP1 抗体 (AA 151-230) (PE)

This anti-SYAP1 antibody is a 兔 多克隆 antibody detecting SYAP1 in WB 和 FACS. Suitable for 人 和 大鼠.
产品编号 ABIN6988112
发货至: 中国

Quick Overview for SYAP1 抗体 (AA 151-230) (PE) (ABIN6988112)

抗原

SYAP1 (Synapse Associated Protein 1 (SYAP1))

适用

人, 大鼠

宿主

  • 26

克隆类型

  • 26
多克隆

标记

  • 7
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SYAP1 antibody is conjugated to PE

应用范围

  • 25
  • 13
  • 13
  • 13
  • 10
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS)
  • 抗原表位

    • 15
    • 8
    • 2
    • 1
    • 1
    AA 151-230

    交叉反应

    人, 大鼠

    预测反应

    Mouse,Dog,Cow,Pig,Horse,Chicken

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human SYAP1

    亚型

    IgG
  • 应用备注

    FCM 1:20-100

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    SYAP1 (Synapse Associated Protein 1 (SYAP1))

    别名

    SYAP1

    背景

    Synonyms: PRO3113, Synapse-associated protein 1, SYAP1

    Background: SYAP1 (synapse-associated protein 1) is a 352 amino acid protein that is ubiquitously expressed in adult tissues. SYAP1 contains one BSD domain which is a novel domain that is present in basal transcription factors, synapse-associated proteins and several hypothetical proteins. The BSD domain is characterized by three predicted alpha helices and by conserved tryptophan and phenylalanine residues, located at the C-terminus of the domain. The gene that encodes SYAP1 in humans is located on chromosome X. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.

    基因ID

    94056

    UniProt

    Q96A49
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