Anti-Human AHI1 Polyclonal Antibody

Categories: [ Antibodies][ Polyclonal Antibodies]

This gene is apparently required for both cerebellar and cortical development in humans. This gene mutations cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci. Alternatively spliced transcript variants encoding different isoforms have been identified.

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Properties

Data Sheet	Click for Datasheet
Catalog Number	PA07336
Size	100μl
Host Type	Rabbit
Immunogen	Synthetic peptide of human AHI1
Specificity	Highly expressed in the most primitive normal hematopoietic cells. Expressed in brain, particularly in neurons that give rise to the crossing axons of the corticospinal tract and superior cerebellar peduncles. Expressed in kidney (renal collecting duct cells) (at protein level).
Isotype	IgG
Reacitivity	Human
Clone
Uniprot	Q8N157
Concentration	0.4 mg/mL
Dilution	IHC 1:25-100, ELISA 1:2000-5000
Formulation
Application	IHC,ELISA
Other Names	Abelson helper integration site 1,Abelson helper integration site 1 protein homolog,Abelson helper integration site,AHI 1,AHI-1,Ahi1,AHI1,Contatins SH3 and WD40 domains,dJ71N10.1,DKFZp686J1653,FLJ14023,FLJ20069,JBTS3,Jouberin,ORF1,OTTHUMP00000017263,OTTHUMP00000017265,OTTHUMP00000234456,OTTHUMP00000234654,OTTHUMP00000234656
Storage	Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript	For research use only, not for use in diagnostic procedures.

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Anti-Human AHI1 Polyclonal Antibody

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