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LEMD3 抗体 (AA 535-852)

This anti-LEMD3 antibody is a 兔 多克隆 antibody detecting LEMD3 in WB, FACS 和 ELISA. Suitable for 人.
产品编号 ABIN7601987
发货至: 中国

Quick Overview for LEMD3 抗体 (AA 535-852) (ABIN7601987)

抗原

See all LEMD3 抗体
LEMD3 (LEM Domain Containing 3 (LEMD3))

适用

  • 10
  • 4
  • 3
  • 3
  • 1

宿主

  • 6
  • 4

克隆类型

  • 6
  • 4
多克隆

标记

  • 10
This LEMD3 antibody is un-conjugated

应用范围

  • 10
  • 7
  • 5
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  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS), ELISA
  • 抗原表位

    • 2
    • 1
    • 1
    AA 535-852

    原理

    Anti-LEMD3 Antibody Picoband®

    交叉反应 (详细)

    No cross reactivity with other proteins.

    产品特性

    Anti-LEMD3 Antibody Picoband® (ABIN7601987). Tested in ELISA, WB, Flow Cytometry applications. This antibody reacts with Human. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human LEMD3 recombinant protein (Position: H535-H852).

    亚型

    IgG
  • 应用备注

    Western blot, 0.25-0.5 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Butkus, C. E., Michels, V. V., Lindor, N. M., Cooney, W. P., III. Melorheostosis in a patient with familial osteopoikilosis. Am. J. Med. Genet. 72: 43-46, 1997. 2. Debeer, P., Pykels, E., Lammens, J., Devriendt, K., Fryns, J.-P. Melorheostosis in a family with autosomal dominant osteopoikilosis: report of a third family. Am. J. Med. Genet. 119A: 188-193, 2003. 3. Hellemans, J., Preobrazhenska, O., Willaert, A., Debeer, P., Verdonk, P. C. M., Costa, T., Janssens, K., Menten, B., Van Roy, N., Vermeulen, S. J. T., Savarirayan, R., Van Hul, W., and 9 others. Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis. Nature Genet. 36: 1213-1218, 2004.

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    浓度

    500 μg/mL

    缓冲液

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    储存条件

    4 °C,-20 °C

    储存方法

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • 抗原

    LEMD3 (LEM Domain Containing 3 (LEMD3))

    别名

    LEMD3

    背景

    Synonyms: 70 kDa ribosomal protein S6 kinase 1 antibody, KS6B1_HUMAN antibody, p70 alpha antibody, P70 beta 1 antibody, p70 ribosomal S6 kinase alpha antibody, p70 ribosomal S6 kinase beta 1 antibody, p70 S6 kinase alpha antibody, P70 S6 Kinase antibody, p70 S6 kinase alpha 1 antibody, p70 S6 kinase alpha 2 antibody, p70 S6K antibody, p70 S6K-alpha antibody, p70 S6KA antibody, p70(S6K) alpha antibody, p70(S6K)-alpha antibody, p70-alpha antibody, p70-S6K 1 antibody, p70-S6K antibody, P70S6K antibody, P70S6K1 antibody, p70S6Kb antibody, PS6K antibody, Ribosomal protein S6 kinase 70 kDa polypeptide 1 antibody, Ribosomal protein S6 kinase beta 1 antibody, Ribosomal protein S6 kinase beta-1 antibody, Ribosomal protein S6 kinase I antibody, RPS6KB1 antibody, S6K antibody, S6K-beta-1 antibody, S6K1 antibody, Serine/threonine kinase 14 alpha antibody, Serine/threonine-protein kinase 14A antibody, STK14A antibody

    Tissue Specificity: Expressed in all tissues.

    Background: LEM domain-containing protein 3 (LEMD3), also known as MAN1, is an integral protein in the inner nuclear membrane (INM) of the nuclear envelope. It is encoded by the LEMD3 gene[5] and was first identified after it was isolated from the serum of a patient with a collagen vascular disease. This locus encodes a LEM domain-containing protein. The encoded protein functions to antagonize transforming growth factor-beta signaling at the inner nuclear membrane. Two transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis.

    分子量

    120 kDa

    基因ID

    23592

    UniProt

    Q9Y2U8
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