Anti FRMD7 pAb (ATL-HPA000886)

Atlas Antibodies

Catalog No.: ATL-HPA000886-25

Protein Description: FERM domain containing 7
Gene Name: FRMD7
Alternative Gene Name: FLJ43346, NYS, NYS1
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000036131: 77%, ENSRNOG00000024762: 79%
Entrez Gene ID: 90167
Uniprot ID: Q6ZUT3
Buffer: 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.
Storage Temperature: Store at +4°C for short term storage. Long time storage is recommended at -20°C.

Product Specifications

• Application: IHC
• Reactivity: Human
• Clonality: Polyclonal
• Host: Rabbit
• Immunogen: QVPRWSPIRAEERTSPHSYVEPTAMKPAERSPRNIRMKSFQQDLQVLQEAIARTSGRSNINVGLEEEDPNLEDAFVCNIQEQTPKRSQSQSDMKTIRFPFGSEFRPLGPCPALSHKADLFTDMFAEQELPAVLMDQSTAERYVASESSDS
• Gene Sequence: QVPRWSPIRAEERTSPHSYVEPTAMKPAERSPRNIRMKSFQQDLQVLQEAIARTSGRSNINVGLEEEDPNLEDAFVCNIQEQTPKRSQSQSDMKTIRFPFGSEFRPLGPCPALSHKADLFTDMFAEQELPAVLMDQSTAERYVASESSDS
• Gene ID - Mouse: ENSMUSG00000036131
• Gene ID - Rat: ENSRNOG00000024762
• Buffer: 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.

Citations for Anti FRMD7 pAb (ATL-HPA000886) – 4 Found

Bolander, Asa; Agnarsdóttir, Margrét; Strömberg, Sara; Ponten, Fredrik; Hesselius, Patrik; Uhlen, Mathias; Bergqvist, Michael. The protein expression of TRP-1 and galectin-1 in cutaneous malignant melanomas. Cancer Genomics & Proteomics. 2008;5(6):293-300. 

Betts-Henderson, Joanne; Bartesaghi, Stefano; Crosier, Moira; Lindsay, Susan; Chen, Hai-Lan; Salomoni, Paolo; Gottlob, Irene; Nicotera, Pierluigi. The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development. Human Molecular Genetics. 2010;19(2):342-51. 

Pu, Jiali; Li, Yingzhi; Liu, Zhirong; Yan, Yaping; Tian, Jun; Chen, Sheng; Zhang, Baorong. Expression and localization of FRMD7 in human fetal brain, and a role for F-actin. Molecular Vision. 2011;17( 21386928):591-7. 

Watkins, Rachel J; Patil, Rajashree; Goult, Benjamin T; Thomas, Mervyn G; Gottlob, Irene; Shackleton, Sue. A novel interaction between FRMD7 and CASK: evidence for a causal role in idiopathic infantile nystagmus. Human Molecular Genetics. 2013;22(10):2105-18.