供货周期: | 现货 |
品牌: | 康朗生物 |
规格: | 0.1ml/0.2ml |
货号: | KL16003R |
CAS号: |
Quantity size:
0.2ml
Concentration:
1mg/ml FAM55A蛋白抗体 Buffer = 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Background:
With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorFAM55A蛋白抗体der known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11. The FAM55A gene product has been provisionally designated FAM55A pending further characterization.
FAM55A蛋白抗体Also known as:
FA55A_HUMAN; FAM55A; Family with sequence similarity 55, member A; Hypothetical protein LOC120400; MGC34290; Neurexophilin and PC-esterase domain family, member 1; NXPE family member 1; NXPE1; OTTHUMP00000238511; Protein FAM55A.
Specificity:
●
Rabbit Polyclonal IgG,FAM55A蛋白抗体 affinity purified by Protein A.
●
Reacts with: Human, .
●
Immunogen: KLH conjugated synthetic peptide derived from human FAM55A.
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Predicted Molecular Weight: 61kDa.
FAM55A蛋白抗体Storage:
Shipped at 4℃, Store at -20℃ (Avoid repeated freeze/thaw cycles).
Application:
WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500
Not yet tested in other applications.
Optimal working dilutions must be determined by the end user.
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