HFE polyclonal antibody (A01)
產品名稱： HFE polyclonal antibody (A01)
英文名稱： HFE polyclonal antibody (A01)
產品編號： H00003077-A01
產品價格： null
產品產地： 臺灣
品牌商標： Abnova
更新時間： null
使用范圍：
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:
- Mouse polyclonal antibody raised against a partial recombinant HFE.
- Immunogen:
- HFE (NP_000401, 115 a.a. ~ 205 a.a) partial recombinant protein with GST tag.
- Sequence:
- SHTLQVILGCEMQEDNSTEGYWKYGYDGQDHLEFCPDTLDWRAAEPRAWPTKLEWERHKIRARQNRAYLERDCPAQLQQLLELGRGVLDQQ
- Host:
- Mouse
- Reactivity:
- Human
- Storage Buffer:
- 50 % glycerol
- Storage Instruction:
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody Reactive Against Recombinant Protein.
- MSDS:
Download
- Application Image
- ELISA
- Entrez GeneID:
- 3077
- GeneBank Accession#:
- NM_000410
- Protein Accession#:
- NP_000401
- Gene Name:
- HFE
- Gene Alias:
- HFE1,HH,HLA-H,MGC103790,dJ221C16.10.1
- Gene Description:
- hemochromatosis
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The protein encoded by this gene is a membrane protein that is similar to MHC class I-type proteins and associates with beta2-microglobulin (beta2M). It is thought that this protein functions to regulate iron absorption by regulating the interaction of the transferrin receptor with transferrin. The iron storage disorder, hereditary haemochromatosis, is a recessive genetic disorder that results from defects in this gene. At least nine alternatively spliced variants have been described for this gene. Additional variants have been found but their full-length nature has not been determined. [provided by RefSeq
- Other Designations:
- MHC class I-like protein HFE,hemochromatosis protein,hereditary hemochromatosis protein HLA-H
- Related Disease
- Abortion, Spontaneous
- Activated Protein C Resistance
- Acute Disease
- Adenocarcinoma
- Adenoma
- Adenomatous Polyps
- Albuminuria
- Alcoholism
- alpha 1-Antitrypsin Deficiency
- alpha-Thalassemia
- Alzheimer Disease
- Alzheimer disease
- Amyotrophic Lateral Sclerosis
- Amyotrophic lateral sclerosis
- Anemia
- Anemia, Iron-Deficiency
- Anemia, Sickle Cell
- Anemia, sickle cell
- Arteriosclerosis