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Invitrogen™ MAGED2 Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA599774
Description
Antibody detects endogenous levels of total MAGD2.
This gene is a member of the MAGED gene family. The MAGED genes are clustered on chromosome Xp11. This gene is located in Xp11.2, a hot spot for X-linked intellectual disability (XLID). Mutations in this gene cause a form of transient antenatal Bartter's syndrome. This gene may also be involved in several types of cancer, including breast cancer and melanoma. The protein encoded by this gene is progressively recruited from the cytoplasm to the nucleoplasm during the interphase and after nucleolar stress and is thus thought to play a role in cell cycle regulation. Alternative splicing results in multiple transcript variants.
Specifications
MAGED2 | |
Polyclonal | |
Unconjugated | |
MAGED2 | |
11B6; 4833439A22Rik; BARTS5; BCG1; BCG-1; Breast cancer-associated gene 1 protein; HCA10; hepatocellular carcinoma-associated protein JCL-1; JCL-1; MAGE family member D2; MAGED; MAGED2; MAGE-D2; MAGE-D2 antigen; melanoma antigen family D, 2; melanoma antigen family D2; melanoma antigen, family D, 2; melanoma-associated antigen D2; MGC8386; ORF1 | |
Rabbit | |
Affinity chromatography | |
RUO | |
10916, 113947, 80884 | |
-20°C | |
Liquid |
Immunohistochemistry (Paraffin), Western Blot | |
1 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 | |
Q9UNF1 | |
MAGED2 | |
A synthesized peptide derived from human MAGED2(Accession Q9UNF1), corresponding to amino acid residues K21-K71. | |
100 μL | |
Primary | |
Human, Mouse, Rat | |
Antibody | |
IgG |
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