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- Home > Products > Proteins/Peptides > Human > Peptides > Membrane > Transporter > FXN (C-term) Peptide
FXN (C-term) Peptide
- カタログ番号 # : P2054
- 頻繁に訪問する :
- サイズ
- 価格
- 在庫あ
- 入手可能
- カート
- 100 ug
- JPY ¥ 20,000
- order now, ship in 5 days
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- この価格は、 Japanでのみ有効です。国を選択して下さい。
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- Specification
- Product Description:
- This synthetic peptide sequence is selected from human FXN construct and is used as the immunogen for PAB2010.
- Sequence:
- C terminus of Human FXN
- Form:
- Lyophilized with 100% acetonitrile
- Storage Buffer:
- Reconstitute with 100 uL deionized water for a final concentration of 1 mg/mL.
- Storage Instruction:
- Store at 4°C. For long term storage store at-20°C.
Aliquot to avoid repeated freezing and thawing.
- Note:
- This product is for research use only. Not for use in diagnostics or therapeutics.
- Application Image
- Blocking
- Entrez GeneID:
- 2395
- Protein Accession#:
- NP_000135;Q16595
- Gene Name:
- FXN
- Gene Alias:
- CyaY,FA,FARR,FRDA,MGC57199,X25
- Gene Description:
- frataxin
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This nuclear gene encodes a mitochondrial protein which belongs to FRATAXIN family. The protein functions in regulating mitochondrial iron transport and respiration. The expansion of intronic trinucleotide repeat GAA results in Friedreich ataxia. Alternative splicing results in multiple transcript variants. [provided by RefSeq
- Other Designations:
- OTTHUMP00000021428
- Related Disease
- Cardiomegaly
- Cardiomyopathies
- Cardiovascular Diseases
- Cerebellar Ataxia
- Chronic Disease
- Diabetes Mellitus, Type 2
- Disease Progression
- Edema
- Fragile X Syndrome
- Fragile X syndrome
- Friedreich Ataxia
- Friedreich's ataxia
- Genetic Predisposition to Disease
- Glucose Intolerance
- Interview, Psychological
- Muscular Atrophy, Spinal
- Myocardial Infarction
- Myotonic Dystrophy
- Myotonic dystrophy
