SH3PXD2B 产品
(SH3 and PX Domains 2B (SH3PXD2B))
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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].
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SH3PXD2B 抗体
High quality antibodies with extensive validation data.
SH3PXD2B 蛋白
Proteins for various applications incl. WB, ELISA, IF etc.
Recommended SH3PXD2B 抗体
Product
Reactivity
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Cat. No.
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Reactivity
Human
Application
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- (2)
Cat. No.
ABIN6244202
Quantity
200 μL
Datasheet
Datasheet
Reactivity
Human
Application
WB
Validations
- (1)
Cat. No.
ABIN6244203
Quantity
200 μL
Datasheet
Datasheet
Reactivity
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Application
IP
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Cat. No.
ABIN7451528
Quantity
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Datasheet
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Recommended SH3PXD2B 蛋白
Latest Publications for our SH3PXD2B Products
: "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).Synonyms and alternative names related to SH3PXD2B
SH3 and PX domains 2B (SH3PXD2B), SH3 and PX domains 2B (Sh3pxd2b), FAD49, fad49, FTHS, G431001E03Rik, HOFI, KIAA1295, TKS4, TSK4Protein level used designations for SH3PXD2B
- SH3 and PX domain-containing protein 2B
- adapter protein HOFI
- adaptor protein HOFI
- factor for adipocyte differentiation 49
- tyrosine kinase substrate with four SH3 domains
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