TSPYL1 Antibody

Code CSB-PA065090
Size US$166
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  • Gel: 8%SDS-PAGE,Lysate: 40 μg,Lane 1-2: Mouse brain tissue, Mouse heart tissue,Primary antibody: CSB-PA065090(TSPYL1 Antibody) at dilution 1/200 dilution,Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution,Exposure time: 2 minutes
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Product Details

Uniprot No.
Target Names
TSPYL1
Alternative Names
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
Raised in
Rabbit
Species Reactivity
Human,Mouse
Immunogen
Synthetic peptide of Human TSPYL1
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Isotype
IgG
Purification Method
Antigen affinity purification
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
Form
Liquid
Tested Applications
ELISA,WB
Recommended Dilution
Application Recommended Dilution
ELISA 1:2000-1:5000
WB 1:500-1:2000
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
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.

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Target Background

Gene References into Functions
  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
Involvement in disease
Sudden infant death with dysgenesis of the testes syndrome (SIDDT)
Subcellular Location
Nucleus, nucleolus.
Protein Families
Nucleosome assembly protein (NAP) family
Tissue Specificity
Expressed in testis, ovary, liver, spleen, brain, kidney, prostate, lung, liver, and heart.
Database Links

HGNC: 12382

OMIM: 604714

KEGG: hsa:7259

STRING: 9606.ENSP00000357597

UniGene: Hs.458358

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