SAMD9L antibody (AA 1223-1557) (FITC)

Catalog No. ABIN8042757

The Rabbit Polyclonal anti-SAMD9L antibody is suitable to detect SAMD9L in samples from Human. It has been validated for FACS.

Quick Overview for SAMD9L antibody (AA 1223-1557) (FITC) (ABIN8042757)

Target: SAMD9L (Sterile alpha Motif Domain Containing 9-Like (SAMD9L))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SAMD9L antibody is conjugated to FITC

Application: Flow Cytometry (FACS)

Product Details anti-SAMD9L Antibody (FITC)

Binding Specificity: AA 1223-1557

Purpose: Anti-SAMD9L Antibody FITC Conjugated

Cross-Reactivity (Details): No cross reactivity with other proteins.

Predicted Reactivity: Human SAMD9L shares 69.3% amino acid (aa) sequence identity with mouse SAMD9L,respectively.

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human SAMD9L recombinant protein (Position: L1223-R1557). Human SAMD9L shares 69.3% amino acid (aa) sequence identity with mouse SAMD9L, respectively.

Isotype: IgG

Application Details

Application Notes: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Expiry Date: 12 months

Target Details for SAMD9L

Target: SAMD9L (Sterile alpha Motif Domain Containing 9-Like (SAMD9L))

Alternative Name: SAMD9L

Background:

Background: This gene encodes a cytoplasmic protein that acts as a tumor suppressor but also plays a key role in cell proliferation and the innate immune response to viral infection. The encoded protein contains an N-terminal sterile alpha motif domain. Naturally occurring mutations in this gene are associated with myeloid disorders such as juvenile myelomonocytic leukemia, acute myeloid leukemia, and myelodysplastic syndrome. Naturally occurring mutations are also associated with hepatitis-B related hepatocellular carcinoma, normophosphatemic familial tumoral calcinosis, and ataxia-pancytopenia syndrome.

Gene Full Name: sterile alpha motif domain containing 9 like

Gene ID: 219285

UniProt: Q8IVG5