SHOX2 Antibody
Product Specifications
Background
This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants.
NCBI Gene ID
6474
Swiss Prot
O60902
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 96-355 of human SHOX2 (NP_003021.3) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Transcription
Purification
Affinity purification
Positive Control
NCI-H460
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Product Datasheet
https://www.prosci-inc.com/?datasheet_sku=23-501
Calculated Molecular Weight
Observed: 30kDa
Fragment
IgG
Applications Notes
WB: 1:500 - 1:2000
Symbol
SHOX2
Positive Control 2
Mouse skeletal muscle
Positive Control 3
Mouse liver
NCBI Official Name
Short stature homeobox 2
NCBI Organism
Homo sapiens
Other Product Names
SHOX2, OG12, OG12X, OGI2X, SHOT
Tested Applications
WB
Physical Properties
Liquid
Curated Selection
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