Solute Carrier Family 35, Member G5 (SLC35G5) (N-Term) antibody

Antigen: Solute Carrier Family 35, Member G5 (SLC35G5)

Binding Site: N-Term

Clonality: Polyclonal

Host: Rabbit

Reactivity: Human

Application: Western Blotting (WB), ELISA

Certificates: ISO 9001:2008

Catalog no.: ABIN654847

Additional Information

Alternative name: AMAC1L2

Gene ID: 83650

UniProt: Q96KT7, NP_473369.1

Immunogen: This AMAC1L2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human AMAC1L2.

Isotype: Ig

Description: Other names: Protein AMAC1L2,AMAC1L2,AMAC

Characteristics: Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)

Specificity: This AMAC1L2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human AMAC1L2.

Molecular Weight: 35161 DA

Comments:

Background: This gene seems to be intronless. It has high sequence similarity to the gene encoding acyl-malonyl condensing enzyme on chromosome 17.

Application Details

Application Notes: The suggested dilution is: ELISA ~~ 1:1,000 Western blotting~~ 1:100~500

Concentration: 0.25 mg/ml

Purification: Purified

Buffer: Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.

Storage: Maintain refrigerated at 2-8 deg C for up to 6 months. For long term storage store at -20 deg C in small aliquots to prevent freeze-thaw cycles

Research Area: Cell Structure

Restrictions: For Research Use only

Images

AMAC1L2 Antibody (N-term) (ABIN654847) western blot analysis in WiDr cell line lysates (35ug/lane). This demonstrates the AMAC1L2 antibody detected the AMAC1L2 protein (arrow).

Publications

Product: Appel, Filter, Reis et al.: "Physical and transcriptional map of the critical region for keratolytic winter erythema (KWE) on chromosome 8p22-p23 between D8S550 and D8S1759." in: European journal of human genetics : EJHG, Vol. 10, Issue 1, pp. 17-25, 2002 (PubMed).

Xing, Wang, Belancio et al.: "Emergence of primate genes by retrotransposon-mediated sequence transduction." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 103, Issue 47, pp. 17608-13, 2006 (PubMed).

Kathiresan, Willer, Peloso et al.: "Common variants at 30 loci contribute to polygenic dyslipidemia." in: Nature genetics, Vol. 41, Issue 1, pp. 56-65, 2008 (PubMed).