Very Low Density Lipoprotein (VLDL) (AA 484-510) antibody

Catalog No. ABIN5535682

This anti- antibody is a Rabbit Polyclonal antibody detecting in WB, FACS and IHC (p). Suitable for Human.

Quick Overview for Very Low Density Lipoprotein (VLDL) (AA 484-510) antibody (ABIN5535682)

Target: Very Low Density Lipoprotein (VLDL)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: Un-conjugated

Application: Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details

Binding Specificity: AA 484-510

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This VLDLR antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 484-510 amino acids from the Central region of human VLDLR.

Isotype: Ig Fraction

Application Details

Application Notes: For FACS starting dilution is: 1:25

For IHC-P starting dilution is: 1:25

For WB starting dilution is: 1:2000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Storage Comment: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Target Details

Target: Very Low Density Lipoprotein (VLDL)

Alternative Name: VLDL

Background: The low density lipoprotein receptor (LDLR) gene family consists of cell surface proteins involved in receptor-mediated endocytosis of specific ligands. This gene encodes a lipoprotein receptor that is a member of the LDLR family and plays important roles in VLDL-triglyceride metabolism and the reelin signaling pathway. Mutations in this gene cause VLDLR-associated cerebellar hypoplasia. Alternative splicing generates multiple transcript variants encoding distinct isoforms for this gene. [provided by RefSeq].

Molecular Weight: 96 kDa

Gene ID: 7436

UniProt: P98155