SLC33A1 antibody (AA 110-190)

Catalog No. ABIN7227166

This Rabbit Polyclonal antibody specifically detects SLC33A1 in WB and ELISA. It exhibits reactivity toward Human, Mouse and Rat.

Quick Overview for SLC33A1 antibody (AA 110-190) (ABIN7227166)

Target: SLC33A1 (Solute Carrier Family 33 Member 1 (SLC33A1))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLC33A1 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-SLC33A1 Antibody

Binding Specificity: AA 110-190

Purpose: Rabbit Anti-ACATN Polyclonal Antibody

Specificity: The antibody detects endogenous levels of ACATN protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from part region of human ACATN protein at AA range: 110-190

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Preservative: ProClin

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

Storage: -20 °C

Storage Comment: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for SLC33A1

Target: SLC33A1 (Solute Carrier Family 33 Member 1 (SLC33A1))

Alternative Name: ACATN

Background: Acetyl-coenzyme A transporter 1, AT-1, Acetyl-CoA transporter 1, Solute carrier family 33 member 1SLC33A1 (Solute Carrier Family 33 Member 1) is a Protein Coding gene. Diseases associated with SLC33A1 include Congenital Cataracts, Hearing Loss, And Neurodegeneration and Spastic Paraplegia 42, Autosomal Dominant. Among its related pathways are Metabolism and Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds.

Molecular Weight: 60kD

Gene ID: 9197

UniProt: O00400