Leucine-Rich Repeat Protein SHOC-2 (SHOC2) Antibody

195€ (20 µl)
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935106861
info@markelab.com
name
Leucine-Rich Repeat Protein SHOC-2 (SHOC2) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx003107
tested applications
ELISA, WB, IF/ICC
Description
SHOC2 Antibody is a Rabbit Polyclonal antibody against SHOC2. This gene encodes a protein that consists almost entirely of leucine-rich repeats, a domain implicated in protein-protein interactions. The protein may function as a scaffold linking RAS to downstream signal transducers in the RAS/ERK MAP kinase signaling cascade. Mutations in this gene have been associated with Noonan-like syndrome with loose anagen hair.
Documents del producto
Instrucciones
Data sheet
Product specifications
Category | Primary Antibodies |
Immunogen Target | Leucine-Rich Repeat Protein SHOC-2 (SHOC2) |
Host | Rabbit |
Reactivity | Human, Mouse, Rat |
Recommended Dilution | ELISA: 1 µg/ml, WB: 1/500 - 1/2000, IF/ICC: 1/50 - 1/100. Optimal dilutions/concentrations should be determined by the end user. |
Clonality | Polyclonal |
Conjugation | Unconjugated |
Isotype | IgG |
Purification | Purified by affinity chromatography. |
Size 1 | 20 µl |
Size 2 | 100 µl |
Size 3 | 2 × 100 µl |
Form | Liquid |
Tested Applications | ELISA, WB, IF/ICC |
Buffer | PBS, pH 7.3, containing 0.01% thimerosal, 50% glycerol. |
Availability | Shipped within 5-10 working days. |
Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
UniProt ID | Q9UQ13 |
Gene ID | 8036 |
NCBI Accession | NP_031399.2 |
Background | Antibody anti-SHOC2 |
Status | RUO |
Note | Concentration: > 0.2 mg/ml - |
Descripción
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Leucine-Rich Repeat Protein SHOC-2 (SHOC2) Antibody
SHOC2 Antibody is a Rabbit Polyclonal antibody against SHOC2. This gene encodes a protein that consists almost entirely of leucine-rich repeats, a domain implicated in protein-protein interactions. The protein may function as a scaffold linking RAS to downstream signal transducers in the RAS/ERK MAP kinase signaling cascade. Mutations in this gene have been associated with Noonan-like syndrome with loose anagen hair.
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