Recombinant Human ANOS1 Protein, His-tagged

• Cat.No.: ANOS1-158H
• Product Overview: Recombinant Human ANOS1 Protein (Ser283-Leu665) with N-His tag was expressed in E. coli.

Specification

• Description: 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.
• Source: E. coli
• Species: Human
• Tag: N-His
• Form: Freeze-dried powder
• Molecular Mass: Predicted Molecular Mass: 46.6 kDa
  Accurate Molecular Mass: 47 kDa
• Protein length: Ser283-Leu665
• Purity: > 90%
• Applications: Positive Control; Immunogen; SDS-PAGE; WB.
• Stability: The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37 centigrade for 48h, and no obvious degradation and precipitation were observed. The loss rate is less than 5% within the expiration date under appropriate storage condition.
• Storage: Avoid repeated freeze/thaw cycles. Store at 2-8 centigrade for one month. Aliquot and store at -80 centigrade for 12 months.
• Storage Buffer: PBS, pH7.4, containing 0.01% SKL, 1 mM DTT, 5% Trehalose and Proclin300.
• Reconstitution: Reconstitute in sterile water to a concentration of 0.1-1.0 mg/mL. Do not vortex.

Gene Information

• Gene Name: ANOS1 anosmin 1 [ Homo sapiens (human) ]
• Official Symbol: ANOS1
• Synonyms: ANOS1; anosmin 1; HH1; HHA; KAL; KMS; KAL1; ADMLX; WFDC19; KALIG-1; anosmin-1; Kallmann syndrome interval gene 1; Kallmann syndrome-1 sequence (anosmin-1); WAP four-disulfide core domain 19; adhesion molecule-like X-linked; kallmann syndrome protein; EC 3.4.21.4
• Gene ID: 3730
• mRNA Refseq: NM_000216
• Protein Refseq: NP_000207
• MIM: 300836
• UniProt ID: P23352