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SH3PXD2B 抗体

(SH3 and PX Domains 2B (SH3PXD2B))
This gene encodes an adapter protein that is characterized by a PX domain and four Src homology 3 domains. The encoded protein is required for podosome formation and is involved in cell adhesion and migration of numerous cell types. Mutations in this gene are the cause of Frank-ter Haar syndrome. [provided by RefSeq, Sep 2010].
SH3PXD2B 抗体  (AA 596-628) SH3PXD2B 抗体  (AA 596-628) SH3PXD2B 抗体 (AA 596-628) (ABIN6244202)

SH3PXD2B 适用: 人 WB, FACS 宿主: 兔 Polyclonal RB55314 unconjugated

SH3PXD2B 抗体 SH3PXD2B 抗体 SH3PXD2B 抗体 (ABIN5587869)

SH3PXD2B 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated

SH3PXD2B 抗体  (AA 505-539) SH3PXD2B 抗体  (AA 505-539) SH3PXD2B 抗体 (AA 505-539) (ABIN6244203)

SH3PXD2B 适用: 人 WB 宿主: 兔 Polyclonal RB55132 unconjugated

SH3PXD2B 抗体 by 适用

Find SH3PXD2B 抗体 for a variety of species such as anti-Human SH3PXD2B. The species listed below are among those available. Click on a link to go to the corresponding products.

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Find SH3PXD2B 抗体 validated for a specific application such as WB, IP, FACS, IHC (p). Some of the available applications are listed below. Click on a link to go to the corresponding products.

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SH3PXD2B 抗体 by 抗原表位

Find SH3PXD2B 抗体 with a specific epitope. The epitopes listed below are among those available. Click on a link to go to the corresponding products.

SH3PXD2B 抗体 by 克隆形成能力

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SH3PXD2B 抗体 by 克隆

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Popular SH3PXD2B 抗体

Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Application WB, FACS
Validations
  • (2)
Cat. No. ABIN6244202
Quantity 200 μL
Datasheet Datasheet
Reactivity Human
Application WB, IHC (p)
Validations
  • (2)
Cat. No. ABIN5587869
Quantity 100 μL
Datasheet Datasheet
Reactivity Human
Application WB
Validations
  • (1)
Cat. No. ABIN6244203
Quantity 200 μL
Datasheet Datasheet
Reactivity Human
Application IP
Validations
Cat. No. ABIN7451528
Quantity 100 μg
Datasheet Datasheet
Reactivity Human
Application WB, IP
Validations
Cat. No. ABIN1934643
Quantity 100 μL
Datasheet Datasheet

Latest Publications for our SH3PXD2B 抗体

Wilson, Sunley, Smith, Pope, Bromhead, Fitzpatrick, Di Rocco, van Steensel, Coman, Leventer, Delatycki, Amor, Bahlo, Lockhart: "Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome." in: European journal of human genetics : EJHG, Vol. 22, Issue 6, pp. 741-7, (2014) (PubMed).

Aliases for SH3PXD2B 抗体

SH3 and PX domains 2B (SH3PXD2B) 抗体
SH3 and PX domains 2B (Sh3pxd2b) 抗体
FAD49 抗体
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TSK4 抗体
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