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WDR35 抗体 (AA 871-1170)

This anti-WDR35 antibody (ABIN6150192) is a Rabbit Polyclonal antibody detecting WDR35 in WB, IF. Suitable for Human.
产品编号 ABIN6150192
发货至: 中国

Quick Overview for WDR35 抗体 (AA 871-1170) (ABIN6150192)

抗原

See all WDR35 抗体
WDR35 (WD Repeat Domain 35 (WDR35))

适用

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宿主

  • 9

克隆类型

  • 9
多克隆

标记

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This WDR35 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunofluorescence (IF)
  • 抗原表位

    • 4
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    AA 871-1170

    序列

    CSQPKAAVDT CVHLNQWNKA VELAKNHSMK EIGSLLARYA SHLLEKNKTL DAIELYRKAN YFFDAAKLMF KIADEEAKKG SKPLRVKKLY VLSALLIEQY HEQMKNAQRG KVKGKSSEAT SALAGLLEEE VLSTTDRFTD NAWRGAEAYH FFILAQRQLY EGCVDTALKT ALHLKDYEDI IPPVEIYSLL ALCACASRAF GTCSKAFIKL KSLETLSSEQ KQQYEDLALE IFTKHTSKDN RKPELDSLME GGEGKLPTCV ATGSPITEYQ FWMCSVCKHG VLAQEISHYS FCPLCHSPVG

    交叉反应

    人, 小鼠, 大鼠

    产品特性

    Polyclonal Antibodies

    免疫原

    Recombinant fusion protein containing a sequence corresponding to amino acids 871-1170 of human WDR35 (NP_065830.2).

    亚型

    IgG
  • 应用备注

    WB,1:500 - 1:1000,IF,1:50 - 1:200

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原

    WDR35 (WD Repeat Domain 35 (WDR35))

    别名

    WDR35

    背景

    This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. Two patients with Sensenbrenner syndrome / cranioectodermal dysplasia (CED) were identified with mutations in this gene, consistent with a possible ciliary function.,WDR35,CED2,IFT121,IFTA1,SRTD7,Cell Biology & Developmental Biology,WDR35

    分子量

    132 kDa/133 kDa

    基因ID

    57539

    UniProt

    Q9P2L0

    途径

    Hedgehog Signaling
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