TSPYL1 Antibody

說明書

中文名稱：

TSPYL1兔多克隆抗體
貨號：

CSB-PA288008
規格：

￥1100
圖片：
Gel: 8%SDS-PAGE,Lysate: 40 μg,,Primary antibody: CSB-PA288008(TSPYL1 Antibody) at dilution 1/200 dilution,Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution,Exposure time: 2 minutes
其他：

產品詳情

Uniprot No.：

Q9H0U9
基因名：

TSPYL1
別名：

SIDDT antibody; Testis specific like protein Y encoded antibody; Testis specific Y encoded like protein 1 antibody; Testis-specific Y-encoded-like protein 1 antibody; TSPY like antibody; TSPY like 1 antibody; TSPY like protein 1 antibody; TSPY-like protein 1 antibody; TSPYL antibody; TSPYL1 antibody; TSYL1_HUMAN antibody
宿主：

Rabbit
反應種屬：

Human,Mouse
免疫原：

Synthetic peptide of Human TSPYL1
免疫原種屬：

Homo sapiens (Human)
標記方式：

Non-conjugated
抗體亞型：

IgG
純化方式：

Antigen affinity purification
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
產品提供形式：

Liquid
應用范圍：

ELISA,WB

推薦稀釋比：

Application	Recommended Dilution
ELISA	1:1000-1:2000
WB	1:200-1:1000

Protocols：

ELISA Protocol
Western Blotting (WB) Protocol
儲存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

基因功能參考文獻：
1. Results show that mutations and polymorphisms in the TSPYL1 gene were not associated with sudden infant death syndrome in a cohort of 165 deceased Swiss infants. PMID: 25449952
2. Mutations in the TSPYL1 gene do not seem to play a major role in the pathogenesis of idiopathic male infertility, and mutation screening of the TSPYL1 gene can currently not be recommended in routine diagnostics of idiopathic male infertility. PMID: 22137496
3. The chromatin remodeling factor TSPYL1 had a very similar pattern of expression with an incremental increase in HPFH and decreased expression in deltabeta-thalassemia. PMID: 16952470
4. Mutations in TSPYL1 may contribute to anomalies of testicular development/function. PMID: 19463995
相關疾病：

Sudden infant death with dysgenesis of the testes syndrome (SIDDT)
亞細胞定位：

Nucleus, nucleolus.
蛋白家族：

Nucleosome assembly protein (NAP) family
組織特異性：

Expressed in testis, ovary, liver, spleen, brain, kidney, prostate, lung, liver, and heart.
數據庫鏈接：

HGNC: 12382

OMIM: 604714

KEGG: hsa:7259

STRING: 9606.ENSP00000357597

UniGene: Hs.458358

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