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SCFD2 抗体 (AA 20-585)

This 兔 多克隆 antibody specifically detects SCFD2 in WB, ELISA, FACS 和 IF. It exhibits reactivity toward 人 和 小鼠.
产品编号 ABIN7871879
发货至: 中国
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Quick Overview for SCFD2 抗体 (AA 20-585) (ABIN7871879)

抗原

See all SCFD2 抗体
SCFD2 (Sec1 Family Domain Containing 2 (SCFD2))

适用

  • 26
  • 19
  • 16
  • 2
  • 2
  • 1
  • 1
  • 1
人, 小鼠

宿主

  • 24
  • 2

克隆类型

  • 26
多克隆

标记

  • 8
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SCFD2 antibody is un-conjugated

应用范围

  • 21
  • 13
  • 13
  • 8
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunofluorescence (IF)
  • 抗原表位

    • 15
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 20-585

    原理

    SCFD2 Antibody / Sec1 family domain-containing protein 2

    纯化方法

    Antigen affinity purified

    免疫原

    E. coli-derived recombinant human protein (amino acids K20-H585) was used as the immunogen for the SCFD2 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the SCFD2 antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    4 °C,-20 °C

    储存方法

    After reconstitution, the SCFD2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 抗原

    SCFD2 (Sec1 Family Domain Containing 2 (SCFD2))

    别名

    SCFD2

    背景

    SCFD2 (sec1 family domain containing 2), also known as STXBP1L1 (syntaxinbinding protein 1-like 1), is a 684 amino acid protein suggested to play a role in protein transport. Existing as two alternatively spliced isoforms, SCFD2 is a member of the STXBP/unc-18/SEC1 family and is encoded by a gene that maps to human chromosome 4q12. Chromosome 4 represents approximately 6 % of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntingtoni 1/2s disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease

    UniProt

    Q8WU76
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