视频一区欧美精品日韩制服国产,2023年成人免费视频,国产情侣2020最新视频,精品视频国产香人视频,国自产精品手机在线观看视频,2025年最新国产卡在线

首頁 > 抗體 > 一抗 > 其它 > TSYL1 rabbit pAb
TSYL1 rabbit pAb
商品貨號： PLA020762
適 應(yīng) 性： 人,小鼠
WB
￥600元
規(guī)格：
在線咨詢
MSDS
說明書
商品描述
  • 基因名稱： TSPYL1 TSPYL
  • 蛋白名稱： TSYL1
  • Human_gene_id： 7259
  • Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=7259
  • Human_swiss_prot_no： Q9H0U9
  • Human_swiss_link： https://www.uniprot.org/uniprotkb/Q9H0U9/entry
  • Mouse_gene_id： 22110
  • Mouse_gene_link： https://www.uniprot.org/uniprot/22110
  • Mouse_swiss_prot_no： O88852
  • Mouse_swiss_link： https://www.uniprot.org/uniprotkb/O88852
  • 特異性： This antibody detects endogenous levels of TSYL1 at Human/Mouse
  • 組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來源： Polyclonal, Rabbit,IgG
  • 稀釋： WB 1：500-2000
  • 純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 濃度： 1 mg/ml
  • 儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說明書： 1
  • Msds： MSDS_Antibody.pdf
  • 分子量： 48kD
  • 功能： disease:Defects in TSPYL1 are the cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT) [MIM:608800]. SIDDT is an autosomal recessive disorder. Affected infants appear normal at birth, develop signs of visceroautonomic dysfunction early in life, and die before 12 months of age of abrupt cardiorespiratory arrest. Features included bradycardia, hypothermia, severe gastroesophageal reflux, laryngospasm, bronchospasm, and abnormal cardiorespiratory patterns during sleep. Genotypic males with SIDDT had fetal testicular dysgenesis and ambiguous genitalia, with findings such as intraabdominal testes, dysplastic testes, deficient fetal testosterone production, fusion and rugation of the gonadal sac, and partial development of the penile shaft. Female sexual development was normal. Affected infants had an unusual staccato cry, similar to the cry of a goat.,similarity:Belongs to the nucleosome assembly protein (NAP) family.,tissue specificity:Expressed in testis, ovary, liver, spleen, brain, kidney, prostate, lung, liver, and heart.,
  • 相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
  • 細(xì)胞定位： Nucleus, nucleolus .
  • 組織表達(dá)： Expressed in testis, ovary, liver, spleen, brain, kidney, prostate, lung, liver, and heart.
  • 科研貨號： PLA020762
TSYL1 rabbit pAb
Catalog No PLA020762
Product information
  • 基因名稱： TSPYL1 TSPYL
  • 蛋白名稱： TSYL1
  • Human_gene_id： 7259
  • Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=7259
  • Human_swiss_prot_no： Q9H0U9
  • Human_swiss_link： https://www.uniprot.org/uniprotkb/Q9H0U9/entry
  • Mouse_gene_id： 22110
  • Mouse_gene_link： https://www.uniprot.org/uniprot/22110
  • Mouse_swiss_prot_no： O88852
  • Mouse_swiss_link： https://www.uniprot.org/uniprotkb/O88852
  • 特異性： This antibody detects endogenous levels of TSYL1 at Human/Mouse
  • 組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來源： Polyclonal, Rabbit,IgG
  • 稀釋： WB 1：500-2000
  • 純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 濃度： 1 mg/ml
  • 儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說明書： 1
  • Msds： MSDS_Antibody.pdf
  • 分子量： 48kD
  • 功能： disease:Defects in TSPYL1 are the cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT) [MIM:608800]. SIDDT is an autosomal recessive disorder. Affected infants appear normal at birth, develop signs of visceroautonomic dysfunction early in life, and die before 12 months of age of abrupt cardiorespiratory arrest. Features included bradycardia, hypothermia, severe gastroesophageal reflux, laryngospasm, bronchospasm, and abnormal cardiorespiratory patterns during sleep. Genotypic males with SIDDT had fetal testicular dysgenesis and ambiguous genitalia, with findings such as intraabdominal testes, dysplastic testes, deficient fetal testosterone production, fusion and rugation of the gonadal sac, and partial development of the penile shaft. Female sexual development was normal. Affected infants had an unusual staccato cry, similar to the cry of a goat.,similarity:Belongs to the nucleosome assembly protein (NAP) family.,tissue specificity:Expressed in testis, ovary, liver, spleen, brain, kidney, prostate, lung, liver, and heart.,
  • 相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
  • 細(xì)胞定位： Nucleus, nucleolus .
  • 組織表達(dá)： Expressed in testis, ovary, liver, spleen, brain, kidney, prostate, lung, liver, and heart.
  • 科研貨號： PLA020762
    • Hunan UPT Biotechnology Co.,Ltd
    Website：www.hnntwy.com Servive hotline :4006916686
    E-mail：service@uptbio.com
    Address：
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
普拉特澤實(shí)驗(yàn)室電話助手

4006916686

掃碼咨詢