TET1 Polyclonal Antibody


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Cat.No.:  EAb-0660
Product Name:  TET1 Polyclonal Antibody
Antibody Type:  Polyclonal
Conjugate:  Unconjugated
Host:  Rabbit
Isotype:  IgG
Purification:  Affinity Purified
Appearance:  Liquid
Formulation:  PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Applications:  WB
Recommended Dilutions/Conditions:  WB; Recommended dilution: WB 1:500 -1:2000, IHC 1:50 -1:200
Recommended dilutions/conditions may not be available for all applications. Specific conditions for reactivity should be optimized by the end user.
Species Reactivity:  Human, Mouse, Rat
Storage:  -20°C
Warning:  For Research Use Only! Not For Use in Humans.
Alternative Name:  bA119F7.1 antibody, CXXC 6 antibody, CXXC finger 6 antibody, CXXC type zinc finger protein 6 antibody, KIAA1676 antibody, LCX antibody, Leukemia associated protein with a CXXC domain antibody, Methylcytosine dioxygenase TET1 antibody, Ten eleven translocation 1 antibody, Ten eleven translocation 1 gene protein homolog antibody, Tet 1 antibody, Tet methylcytosine dioxygenase 1 antibody, Tet oncogene 1 antibody, TET1 antibody, TET1_HUMAN antdy
Scientific Background:  TET1 (tet oncogene 1), also known as LCX or CXXC6, is a 2,136 amino acid protein that localizes to the nucleus and contains one CXXC-type zinc finger. Expressed in adult ovary, thymus and skeletal muscle and also present in fetal lung, heart and brain, TET1 is thought to play a role in the development of fetal organs and may also be involvement in the pathoegenesis and metastasis of acute myeloid leukemia (AML). The gene encoding TET1 maps to human chromosome 10, which houses over 1,200 genes and comprises nearly 4. 5% of the human genome. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman's syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

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For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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