GNAT2 Antibody
-
中文名稱:GNAT2兔多克隆抗體
-
貨號:CSB-PA237874
-
規(guī)格:¥2024
-
圖片:
-
其他:
產品詳情
-
產品名稱:Rabbit anti-Homo sapiens (Human) GNAT2 Polyclonal antibody
-
Uniprot No.:
-
基因名:GNAT2
-
宿主:Rabbit
-
反應種屬:Human,Mouse
-
免疫原:Synthesized peptide derived from internal of Human GNAT2.
-
免疫原種屬:Homo sapiens (Human)
-
克隆類型:Polyclonal
-
純化方式:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
-
濃度:It differs from different batches. Please contact us to confirm it.
-
產品提供形式:Liquid
-
應用范圍:ELISA,WB
-
推薦稀釋比:
Application Recommended Dilution WB 1:500-1:3000 -
Protocols:
-
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.
相關產品
靶點詳情
-
功能:Guanine nucleotide-binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems. Transducin is an amplifier and one of the transducers of a visual impulse that performs the coupling between rhodopsin and cGMP-phosphodiesterase.
-
基因功能參考文獻:
- The majority (n = 12) of patients were either homozygotes or compound heterozygotes for known achromatopsia alleles, two in CNGB3 (p.T383fsX and p.T296YfsX9) and three in CNGA3 (p.R283Q, p.R427C and p.L527R). PMID: 23362848
- Single nucleotide polymorphisms in GNAT2 gene is associated with obesity. PMID: 23563607
- Missense mutations, nonsense mutations, splice mutations, and small deletions and insertions in the affected genes cause achromatopsia. PMID: 21267001
- Expression of GNAT2 transgene, when found in rod photoreceptor cells rather than in cones, demonstrates different mechanisms of amplification in the body's G-protein alpha cascades and the activation of phosphodiesterase 6. PMID: 20603337
- Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene. PMID: 21107338
- mutations in GNAT2 are implicated in achromatopsia PMID: 12077706
- We detected a deletion of a highly conserved lysine at codon 270 in a critical functional area of the alpha-cone transducin molecule, and therefore is not the disease causing mutation. PMID: 15094710
顯示更多
收起更多
-
相關疾?。?/div>Achromatopsia 4 (ACHM4)亞細胞定位:Cell projection, cilium, photoreceptor outer segment. Photoreceptor inner segment.蛋白家族:G-alpha family, G(i/o/t/z) subfamily組織特異性:Retinal rod outer segment.數(shù)據(jù)庫鏈接:
Most popular with customers
-
-
YWHAB Recombinant Monoclonal Antibody
Applications: ELISA, WB, IF, FC
Species Reactivity: Human, Mouse, Rat
-
Phospho-YAP1 (S127) Recombinant Monoclonal Antibody
Applications: ELISA, WB, IHC
Species Reactivity: Human
-
-
-
-
-