hspb9
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  • Official Full Name
  • heat shock protein, alpha-crystallin-related, B9
  • Background
  • HSPB9, also known as CT51, belongs to the small heat shock protein (HSP20) family. Localizing to the cytoplasm as well as the nucleus, HSPB9 is expressed specifically in the testis.
  • Synonyms
  • CT51
Cat.#:HSPB9-5123HTag:GST
Source (Host):Wheat GermSpecies:Human
Product nameRecombinant Human HSPB9 Protein, GST-tagged
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Cat.#:HSPB9-15832HTag:His
Source (Host):E. coliSpecies:Human
Product nameRecombinant Human HSPB9, His-tagged
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Cat.#:HSPB9-5581HTag:His
Source (Host):E. coliSpecies:Human
Product nameRecombinant Human Heat Shock Protein, Alpha-crystallin-related, B9, His-tagged
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Cat.#:HSPB9-6468ZTag:His
Source (Host):Mammalian CellsSpecies:Zebrafish
Product nameRecombinant Zebrafish HSPB9
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Cat.#:HSPB9-5344HCLTag:
Source (Host):Species:Human
Product nameRecombinant Human HSPB9 293 Cell Lysate
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Protein Function

HSPB9 has several biochemical functions, for example, protein binding. Some of the functions are cooperated with other proteins, some of the functions could acted by HSPB9 itself. We selected most functions HSPB9 had, and list some proteins which have the same functions with HSPB9. You can find most of the proteins on our site.
Function
Related Protein
Function protein binding
Related Protein PTK6; MYH9; DUSP14; PRPF4; THRB; SS18; USP14; SH3BP1; POLL; C1GALT1C1

Interacting Protein

HSPB9 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with HSPB9 here. Most of them are supplied by our site. Hope this information will be useful for your research of HSPB9.
DYNLT1; CTCF; NUDT5

HSPB9 Related Articles

Xun, WJ; Shi, LG; et al. Dual Functions in Response to Heat Stress and Spermatogenesis: Characterization of Expression Profile of Small Heat Shock Proteins 9 and 10 in Goat Testis. Biomed Research International :-(2015).
Poirsier-Violle, C; Abourra, A; et al. A de novo 17q21.2 duplication in a boy with developmental delay and dysmorphic features. EUROPEAN JOURNAL OF MEDICAL GENETICS 56:226-228(2013).