PTD016 Rabbit pAb
- 产品详情
- 实验流程
Application
| WB, E |
|---|---|
| Primary Accession | Q5M7Z0 |
| Other Accession | Q5M7Z0 |
| Host | Rabbit |
| Clonality | Polyclonal |
| Calculated MW | 49710 Da |
| Physical State | Liquid |
| Immunogen | KLH conjugated synthetic peptide derived from human PTD016 |
| Epitope Specificity | 31-130/435 |
| Isotype | IgG |
| Purity | affinity purified by Protein A |
| Buffer | Preservative: 0.02% Proclin300, Constituents: 1% BSA, 0.01M PBS, pH7.4. |
| Important Note | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| Background Descriptions | RNFT1 (Ring Finger Protein, Transmembrane 1) is a Protein Coding gene. Diseases associated with RNFT1 include Sertoli Cell-Only Syndrome. An important paralog of this gene is RNFT2. |
| Gene ID | 51136 |
|---|---|
| Other Names | PTD016; RNFT1_HUMAN; RNFT1; Protein PTD016; RING finger and transmembrane domain-containing protein 1; 2.3.2.27; ring finger protein, transmembrane 1 |
| Dilution | WB=1:500-2000,ELISA=1:5000-10000 |
| Storage | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. 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. |
For Research Use Only. Not For Use In Diagnostic Procedures.
| Name | RNFT1 |
|---|---|
| Function | E3 ubiquitin-protein ligase that acts in the endoplasmic reticulum (ER)-associated degradation (ERAD) pathway, which targets misfolded proteins that accumulate in the endoplasmic reticulum (ER) for ubiquitination and subsequent proteasome-mediated degradation. Protects cells from ER stress-induced apoptosis. |
| Cellular Location | Endoplasmic reticulum membrane; Multi-pass membrane protein |
| Tissue Location | Expressed at highest levels in testis, lower levels in heart, liver, lung, and kidney (PubMed:17074343). Not detected in brain, ovary, and uterus (PubMed:17074343). Down-regulated in testis from patients with maturation arrest (MA) or Sertoli cell-only syndrome (SCOS) (PubMed:17074343). Ubiquitously expressed with high expression in testis (PubMed:27485036). |
Research Areas
Application Protocols
Provided below are standard protocols that you may find useful for product applications.
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