Anti-Human ANOS1 Polyclonal Antibody

Mutations in this gene cause the X-linked Kallmann syndrome. The encoded protein is similar in sequence to proteins known to function in neural cell adhesion and axonal migration. In addition, this cell surface protein is N-glycosylated and may have anti-protease activity.ANOS1 (Anosmin 1) is a Protein Coding gene. Diseases associated with ANOS1 include Hypogonadotropic Hypogonadism 1 With Or Without Anosmia and Kallmann Syndrome. Among its related pathways are Negative regulation of FGFR1 signaling and Signaling by FGFR2. GO annotations related to this gene include heparin binding and extracellular matrix structural constituent.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA04655
Size 100μl
Host Type Rabbit
Immunogen Synthesized peptide derived from the Internal region of human KALIG-1
Specificity Expressed in the cerebellum (at protein level).
Isotype IgG
Reacitivity Human
Clone
Uniprot P23352
Concentration 1mg/mL
Dilution WB 1:500-1:2000, ELISA 1:10000
Formulation
Application WB,ELISA
Other Names Adhesion molecule-like X-linked,ADMLX,Anosmin-1,HHA,KAL,KAL1,KALIG 1,KALIG1,Kallmann syndrome 1 sequence (anosmin 1),Kallmann syndrome 1 sequence,Kallmann syndrome interval gene 1,Kallmann syndrome protein,KALM,KALM,KMS,OTTHUMP00000022873
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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