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WISP3 抗体 (AA 42-260)

This anti-WISP3 antibody is a 兔 多克隆 antibody detecting WISP3 in WB. Suitable for 人.
产品编号 ABIN7271384
发货至: 中国

Quick Overview for WISP3 抗体 (AA 42-260) (ABIN7271384)

抗原

See all WISP3 抗体
WISP3 (Wnt1 Inducible Signaling Pathway Protein 3 (WISP3))

适用

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宿主

  • 39
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克隆类型

  • 40
多克隆

标记

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This WISP3 antibody is un-conjugated

应用范围

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Western Blotting (WB)
  • 抗原表位

    • 15
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    AA 42-260

    原理

    WISP3 Rabbit pAb

    序列

    TGPLDTTPEG RPGEVSDAPQ RKQFCHWPCK CPQQKPRCPP GVSLVRDGCG CCKICAKQPG EICNEADLCD PHKGLYCDYS VDRPRYETGV CAYLVAVGCE FNQVHYHNGQ VFQPNPLFSC LCVSGAIGCT PLFIPKLAGS HCSGAKGGKK SDQSNCSLEP LLQQLSTSYK TMPAYRNLPL IWKKKCLVQA TKWTPCSRTC GMGISNRVTN ENSNCEMRK

    交叉反应

    人, 小鼠, 大鼠

    产品特性

    Polyclonal Antibodies

    纯化方法

    Affinity purification

    免疫原

    Recombinant fusion protein containing a sequence corresponding to amino acids 42-260 of human WISP3 (NP_937882.1).

    亚型

    IgG
  • 应用备注

    WB,1:500 - 1:2000

    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

    WISP3 (Wnt1 Inducible Signaling Pathway Protein 3 (WISP3))

    别名

    WISP3

    背景

    This gene encodes a member of the WNT1 inducible signaling pathway (WISP) protein subfamily, which belongs to the connective tissue growth factor (CTGF) family. WNT1 is a member of a family of cysteine-rich, glycosylated signaling proteins that mediate diverse developmental processes. The CTGF family members are characterized by four conserved cysteine-rich domains: insulin-like growth factor-binding domain, von Willebrand factor type C module, thrombospondin domain and C-terminal cystine knot-like domain. This gene is overexpressed in colon tumors. It may be downstream in the WNT1 signaling pathway that is relevant to malignant transformation. Mutations of this gene are associated with progressive pseudorheumatoid dysplasia, an autosomal recessive skeletal disorder, indicating that the gene is essential for normal postnatal skeletal growth and cartilage homeostasis. Multiple transcript variants encoding different isoforms have been found for this gene.,WISP3,CCN6,LIBC,PPAC,PPD,WISP-3,Cell Biology & Developmental Biology,Growth factor,Immunology & Inflammation,Stem Cells,Mesenchymal Stem Cells,WISP3

    分子量

    39kDa/41kDa

    基因ID

    8838

    UniProt

    O95389

    途径

    WNT signaling, Growth Factor Binding
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