SAMD9 Polyklonale Antilichaam

Defects in SAMD9 are the cause of normophosphatemic familial tumoral calcinosis (NFTC) . NFTC is an uncommon life-threatening disorder characterized by massive periarticular, and seldom visceral, deposition of calcified tumors.

SAM domain-containing protein 9; SAMD9; SAMD9_HUMAN; sterile alpha mot domain containing 9; Sterile alpha mot domain-containing protein 9; C7orf5.

54809

Human, Mouse, Rat

1501-1589/1589

SAMD9

Unconjugated

KLH conjugated synthetic peptide derived from human SAMD9

ELISA, IHC-P, IHC-F, IF

Purified by Protein A.

1µg/µl

ELISA (ELISA=1:5000-10000), IHC-P (IHC-P=1:100-500), IHC-F (IHC-F=1:100-500), IF (IF=1:50-200)

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

Unmodified

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

54809