SHOX 产品
(Short Stature Homeobox (SHOX))
Categories
This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jul 2008].
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Featured SHOX Categories
Recommended SHOX 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
WB
Validations
- (2)
Cat. No.
ABIN520182
Quantity
50 μg
Datasheet
Datasheet
Reactivity
Human
Application
WB
Validations
- (2)
Cat. No.
ABIN7270286
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human
Application
WB
Validations
- (1)
Cat. No.
ABIN6244069
Quantity
50 μL
Datasheet
Datasheet
Recommended SHOX ELISA试剂盒
Product
Reactivity
Analytical Method
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Analytical Method
Quantitative Sandwich ELISA
Validations
Cat. No.
ABIN6233550
Quantity
96 tests
Datasheet
Datasheet
Recommended SHOX 蛋白
Synonyms and alternative names related to SHOX
short stature homeobox (shox), short stature homeobox (SHOX), GCFX, PHOG, SHOXY, si:ch211-134k13.1, SS, zgc:123182Protein level used designations for SHOX
- short stature homeobox protein
- growth control factor, X-linked
- pseudoautosomal homeobox-containing osteogenic protein
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