FADS2 Rabbit pAb (一抗) | Bioss

bs-11516R

农牧业/家禽抗体

FADS2 Rabbit pAb

脂肪酸脱氢酶2抗体

D6D; DES6; FADSD6; LLCDL2; SLL0262; TU13; 2900042M13Rik; Fads2a; Fadsd2; FADS2_MACFA; FADS2; Delta(6) fatty acid desaturase (D6D | Delta(6) desaturase | Delta-6 desaturase); Fatty acid desaturase 2; 1.14.19.3; FADS2_HUMAN; FADS2_MOUSE; FADS2_PONAB; FADS2_RAT;

Rabbit

KLH conjugated synthetic peptide derived from human FADS2: 221-300/444

IgG

Liquid

affinity purified by Protein A

Polyclonal

52 kDa

47 kDa

1mg/ml

0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.

This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

Members of the fatty acid desaturase (FADS) family, including FADS1, FADS2 and FADS3, regulate the desaturation of fatty acids by introducing double bonds between defined carbons of fatty acyl chains, thereby playing an essential role in the lipid metabolic pathway. Members of this family share N-terminal cytochrome b5-like domains, C-terminal multiple membrane-spanning desaturase regions and 3 histidine box motifs. FADS2 (fatty acid desaturase 2), also known as D6D, DES6, LLCDL2 or TU13, is a 444 amino acid multi-pass membrane protein that localizes to the endoplasmic reticulum and contains one cytochrome b5 heme-binding domain. Expressed in adult and fetal heart and in adult liver, brain, lung and retina, FADS2 functions as a component of a lipid metabolic pathway and catalyzes the first step in the pathway, namely the formation of unsaturated fatty acids from polyunsaturated fatty acids. Defects in the gene encoding FADS2 are the cause of cause of fatty acid delta-6-desaturase deficiency, an affliction that is characterized by skin abnormalities, corneal ulceration and growth failure. Multiple isoforms of FADS2 exist due to alternative splicing events.