FMR1 (Human) Recombinant Protein (Q01)
產品名稱： FMR1 (Human) Recombinant Protein (Q01)
英文名稱： FMR1 (Human) Recombinant Protein (Q01)
產品編號： H00002332-Q01
產品價格： 0
產品產地： 臺灣
品牌商標： Abnova
更新時間： null
使用范圍： null
亞諾法生技股份有限公司（Abnova)
- 聯系人 :
- 地址 : 臺灣臺北市內湖區洲子街 108 號 9 樓
- 郵編 : 11493
- 所在區域 : 臺灣
- 電話 : +886-920**1152 點擊查看
- 傳真 : 點擊查看
- 郵箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Human FMR1 partial ORF ( NP_002015, 121 a.a. - 220 a.a.) recombinant protein with GST-tag at N-terminal.
- Sequence:
- ATKDTFHKIKLDVPEDLRQMCAKEAAHKDFKKAVGAFSVTYDPENYQLVILSINEVTSKRAHMLIDMHFRSLRTKLSLIMRNEEASKQLESSRQLASRFH
- Theoretical MW (kDa):
- 36.74
- Preparation Method:
- in vitro wheat germ expression system
- Purification:
- Glutathione Sepharose 4 Fast Flow
- Storage Buffer:
- 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
- Storage Instruction:
- Store at -80°C. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- 12.5% SDS-PAGE Stained with Coomassie Blue.
- Note:
- Best use within three months from the date of receipt of this protein.
- MSDS:
Download
- Application Image
- Enzyme-linked Immunoabsorbent Assay
- Western Blot (Recombinant protein)
- Antibody Production
- Protein Array
- Entrez GeneID:
- 2332
- GeneBank Accession#:
- NM_002024
- Protein Accession#:
- NP_002015
- Gene Name:
- FMR1
- Gene Alias:
- FMRP,FRAXA,MGC87458,POF,POF1
- Gene Description:
- fragile X mental retardation 1
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The protein encoded by this gene binds RNA and is associated with polysomes. The encoded protein may be involved in mRNA trafficking from the nucleus to the cytoplasm. A trinucleotide repeat (CGG) in the 5' UTR is normally found at 6-53 copies, but an expansion to 55-230 repeats is the cause of fragile X syndrome. Expansion of the trinucleotide repeat may also cause one form of premature ovarian failure (POF1). [provided by RefSeq
- Other Designations:
- OTTHUMP00000024197,premature ovarian failure 1
- Related Disease
- Ataxia
- Ataxia Telangiectasia
- Ataxia telangiectasia
- Attention
- Attention Deficit Disorder with Hyperactivity
- Autistic Disorder
- Cerebellar Ataxia
- Cognition
- Cognition Disorders
- Dementia
- Disease Progression
- Essential Tremor
- Essential tremor
- Fetal Diseases
- Fragile X Syndrome
- Fragile X syndrome
- Genetic Predisposition to Disease
- Genomic Instability
- Hallucinations