KAL1 (ANOS1) (NM_000216) Human Recombinant Protein
Product Specifications
Background
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. [provided by RefSeq, Jul 2008]
Synonyms
ADMLX; HH1; HHA; KAL; KAL1; KALIG-1; KMS; WFDC19
Gene ID
3730
UniProt
P23352
Accession Number mRNA
NM_000216
Chromosomal Location
Xp22.31
Expression System
E. coli
Tag
N-His
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
50mM Tris, 8M Urea, pH8.0.
Molecular Weight
27.5 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
ANOS1
Species
Human
Protein ID
NP_000207
Overview
Purified recombinant protein of Human Kallmann syndrome 1 sequence (KAL1), Val129-Glu373, with N-terminal His tag, expressed in E.coli, 50ug
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/3730
Uniprot URL
https://www.uniprot.org/uniprot/P23352
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_000216
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_000207
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