C8orf78,第8号染色体开放阅读框78抗体

产品编号HZ-16074R
英文名称C8orf78
中文名称第8号染色体开放阅读框78抗体
别 名FER1L6-AS2; FEAS2_HUMAN; C8orf78; FER1L6 antisense gene protein 2; FER1L6 antisense RNA 2; Putative uncharacterized protein encoded by FER1L6-AS2.
说 明 书0.1ml 0.2ml
研究领域细胞生物 免疫学
抗体来源Rabbit
克隆类型Polyclonal
交叉反应Human,
C8orf78,第8号染色体开放阅读框78抗体产品应用WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 （石蜡切片需做抗原修复）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量15kDa
性 状Lyophilized or Liquid
浓 度1mg/1ml
免 疫 原KLH conjugated synthetic peptide derived from human C8orf78
亚 型IgG
纯化方法affinity purified by Protein A
储 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
C8orf78,第8号染色体开放阅读框78抗体PubMedPubMed
产品介绍background:
C8orf78 (chromosome 8 open reading frame 78) is a 137 amino acid protein encoded by a gene that maps to human chromosome 8q24.13. Consisting of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and are typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.

Gene ID:
157376

Database links:
Entrez Gene: 157376 Human
SwissProt: Q96M78 Human

C8orf78,第8号染色体开放阅读框78抗体Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.