TEL: +86 571 56623320 EMAIL: [email protected]
Product Name PDGFRL Chinese Name 血小板源性生长因子受体β样蛋白抗体 Alias PDGF receptor beta like tumor suppressor; PGFRL_HUMAN; PDGFR-like protein; PDGRL; PRLTS. Research Area Tumour immunology Immunogen Species Rabbit Clonality Polyclonal React Species (predicted: Human, Mouse, Rat, Dog, Horse, ) Applications ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.Theoretical molecular weight 40kDa Cellular localization Secretory protein Form Liquid Concentration 1mg/ml immunogen KLH conjugated synthetic peptide derived from human PDGFRL: 61-150/375 Lsotype IgG Purification affinity purified by Protein A Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. PubMed PubMed Product Detail This protein is expressed in colon, lung and liver. Defects in PDGFRL are associated with colorectal cancer.
Subunit:
Forms a complex composed of PDGFRL, TNK2 and GRB2.
Subcellular Location:
Secreted (Probable).
Tissue Specificity:
Expressed in colon, lung and liver.
DISEASE:
Colorectal cancer (CRC) [MIM:114500]: A complex disease characterized by malignant lesions arising from the inner wall of the large intestine (the colon) and the rectum. Genetic alterations are often associated with progression from premalignant lesion (adenoma) to invasive adenocarcinoma. Risk factors for cancer of the colon and rectum include colon polyps, long-standing ulcerative colitis, and genetic family history. Note=The gene represented in this entry is involved in disease pathogenesis.
Note=A polymorphism in PDGFRL has been reported to be associated with susceptibility to Behcet disease (PubMed:19815557). Behcet disease is a complex multiple-system disorder characterized by recurrent oral ulcerations, recurrent genital ulcerations, typical skin lesions, and uveitis. Behcet disease also involves joints, blood vessels, musculoskeletal, neurological systems, and the gastrointestinal tract.
Similarity:
Contains 2 Ig-like C2-type (immunoglobulin-like) domains.
SWISS:
Q15198
Gene ID:
5157
Database links:Entrez Gene: 5157 Human
Entrez Gene: 68797 Mouse
GenBank: NP_006198.1 Human
Omim: 604584 Human
SwissProt: Q15198 Human
SwissProt: Q2PFX1 Monkey
SwissProt: Q6PE55 Mouse
Unigene: 458573 Human
Unigene: 284246 Mouse
Scan Wechat Qrcode
Scan Whatsapp Qrcode