ARG55228

anti-DLK1 antibody

anti-DLK1 antibody for Flow cytometry,IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse

Developmental Biology antibody; Neuroscience antibody; Signaling Transduction antibody

Overview

Product Description Rabbit Polyclonal antibody recognizes DLK1
Tested Reactivity Hu, Ms
Tested Application FACS, IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name DLK1
Antigen Species Human
Immunogen KLH-conjugated synthetic peptide corresponding to aa. 368-402 (C-terminus) of Human DLK1.
Conjugation Un-conjugated
Alternate Names Delta1; ZOG; DLK; FA1; DLK-1; pG2; Pref-1; PREF1; Protein delta homolog 1

Application Instructions

Application Suggestion
Tested Application Dilution
FACS1:25
IHC-PAssay-dependent
WBAssay-dependent
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Positive Control Mouse skeletal muscle

Properties

Form Liquid
Purification Purification with Protein A and immunogen peptide.
Buffer PBS and 0.09% (W/V) Sodium azide
Preservative 0.09% (W/V) Sodium azide
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 13386 Mouse DLK1

GeneID: 8788 Human DLK1

Swiss-port # P80370 Human Protein delta homolog 1

Swiss-port # Q09163 Mouse Protein delta homolog 1

Gene Symbol DLK1
Gene Full Name delta-like 1 homolog (Drosophila)
Background This gene encodes a transmembrane protein containing six epidermal growth factor repeats. The protein is involved in the differentiation of several cell types, including adipocytes; it is also thought to be a tumor suppressor. It is one of several imprinted genes located in a region of on chr 14q32. Certain mutations in this imprinted region can cause phenotypes similar to maternal and paternal uniparental disomy of chromosome 14 (UPD14). This gene is expressed from the paternal allele. A polymorphism within this gene has been associated with child and adolescent obesity. The mode of inheritance for this polymorphism is polar overdominance; this non-Mendelian inheritance pattern was first described in sheep with the callipyge phenotype, which is characterized by muscle hypertrophy and decreased fat mass. [provided by RefSeq, Mar 2010]
Function May have a role in neuroendocrine differentiation. [UniProt]
Cellular Localization Membrane; Single-pass type I membrane protein
Research Area Developmental Biology antibody; Neuroscience antibody; Signaling Transduction antibody
Calculated MW 41 kDa
PTM N- and O-glycosylated. O-glycosylated with core 1 or possibly core 8 glycans.