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The antibody against WBSCR27 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-245 of human WBSCR27 (NP_689772.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, ELISA.
The antibody against WBSCR27 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-245 of human WBSCR27 (NP_689772.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, ELISA.
| Cat.No | ADA-04584A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | WBSCR27 |
| Target Synonyms | WBSCR27 | Form | Liquid |
| Species Reactivity | Human, Mouse, Rat | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.01% thimerosal, pH7.3. | Purification Method | Affinity purification |
| Positive Samples | HT-29, MCF7, Mouse lung | Application | ELISA, WB, IHC-P |
| Immunogen Description | Recombinant fusion protein containing a sequence corresponding to amino acids 1-245 of human WBSCR27 (NP_689772.2). | Target Species | Human |
|---|---|---|---|
| Uniprot ID | Q8N6F8 | Immunogen Sequence |
Uniprot Id
Q8N6F8
Target Species
Human
Target Name
METTL27
Target Full Name
Methyltransferase-like protein 27
Target Involvement
METTL27 is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region. Haploinsufficiency of METTL27 may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in the disease.
Target Research Area
Epigenetics and Nuclear Signaling
Target Synonyms
WBS27_HUMAN; WBSCR27; Williams-Beuren syndrome chromosomal region 27 protein
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