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PCNT 抗体

This anti-PCNT antibody is a 兔 多克隆 antibody detecting PCNT in IHC (p). Suitable for 人 和 小鼠.
产品编号 ABIN7230530
发货至: 中国

Quick Overview for PCNT 抗体 (ABIN7230530)

抗原

See all PCNT 抗体
PCNT (Pericentrin (PCNT))

适用

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人, 小鼠

宿主

  • 11

克隆类型

  • 11
多克隆

标记

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This PCNT antibody is un-conjugated

应用范围

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Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 原理

    PCNT Polyclonal Antibody

    特异性

    The antibody detects endogenous levels of PCNT protein

    纯化方法

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

    免疫原

    Synthesized peptide derived from part region of human PCNT protein

    亚型

    IgG
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: IHC-P (1:50-1:300).

    说明

    Primary Antibody

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

    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

    -20 °C

    储存方法

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • 抗原

    PCNT (Pericentrin (PCNT))

    别名

    PCNT

    背景

    Rabbit Anti-PCNT Polyclonal Antibody,Pericentrin, Kendrin, Pericentrin-B,The protein encoded by PCNT gene binds to calmodulin and is expressed in the centrosome. It is an integral component of the pericentriolar material (PCM). The protein contains a series of coiled-coil domains and a highly conserved PCM targeting motif called the PACT domain near its C-terminus. The protein interacts with the microtubule nucleation component gamma-tubulin and is likely important to normal functioning of the centrosomes, cytoskeleton, and cell-cycle progression. Mutations in this gene cause Seckel syndrome-4 and microcephalic osteodysplastic primordial dwarfism type II. Two transcript variants encoding different isoforms have been found for this gene.,PCNT

    分子量

    observerd band 366kDa

    基因ID

    5116

    UniProt

    O95613

    途径

    Sensory Perception of Sound, M Phase, SARS-CoV-2 Protein Interactome
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