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Invitrogen™ SMYD5 Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA513217
Description
SMYD5 Polyclonal Antibody for Western Blot, IHC (P)
Retinoic acid (RA) represents the oxidized form of vitamin A and, via interactions with retinoic acid receptors (RARs), plays a crucial role in development, cellular growth and differentiation. The gene encoding RAI15 maps to human chromosome 2, which houses over 1,400 genes and comprises nearly 8% of the human genome. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene, while the lipid metabolic disorder sitosterolemia is associated with defects in the ABCG5 and ABCG8 genes. Additionally, an extremely rare recessive genetic disorder, Alström syndrome, is caused by mutations in the ALMS1 gene, which maps to chromosome 2.
Specifications
SMYD5 | |
Polyclonal | |
Unconjugated | |
SMYD5 | |
AW536703; NN8-4AG; Protein NN8 4AG; Protein NN8-4AG; Rai15; retinoic acid induced 15; retinoic acid responsive; retinoic acid responsive gene 1; retinoic acid-induced protein 15; RRG1; SET and MYND domain containing 5; SET and MYND domain-containing protein 5; SMYD family member 5; SMYD5; ZMYND23 | |
Rabbit | |
Ammonium sulfate precipitation, Size-exclusion - Dialysis | |
RUO | |
10322, 232187 | |
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
Liquid |
Immunohistochemistry (Paraffin), Western Blot | |
2 mg/mL | |
PBS with 0.09% sodium azide; pH 7.4 | |
Q3TYX3, Q6GMV2 | |
SMYD5 | |
KLH conjugated synthetic peptide between 341-371 amino acids from the C-terminal region of human SMYD5 (RAI15). | |
400 μL | |
Primary | |
Human, Mouse | |
Antibody | |
IgG |
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