FAM98A Rabbit pAb (一抗) - WB,IHC-P,IHC-F,IF,Flow-Cyt | Bioss

bs-11012R

农牧业/家禽抗体

FAM98A Rabbit pAb

FAM98A蛋白抗体

2810405J04Rik; CR201_G0017884; RGD1305486; FA98A_HUMAN; FAM98A; FA98A_MOUSE; FA98A_PONAB; FA98A_RAT; family with sequence similarity 98 member A; family with sequence similarity 98, member A

Rabbit

KLH conjugated synthetic peptide derived from human FAM98A: 251-350/519

IgG

Liquid

affinity purified by Protein A

Polyclonal

55 kDa

55 kDa

1mg/ml

0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.

This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM98 gene product has been provisionally designated FAM98 pending further characterization.