GH/hPL (ABT540) mouse mAb
- 货号：YM6997
- 应用：IHC;ELISA
- 种属：Human
- 靶点：
- Humanm Placental lactogen
- 简介：
- >>Cytokine-cytokine receptor interaction;>>Neuroactive ligand-receptor interaction;>>PI3K-Akt signaling pathway;>>JAK-STAT signaling pathway;>>Growth hormone synthesis, secretion and action
- 蛋白名称：
- Lactogen
Placental lactogen
PL
hPL
gH
GH-N
GH1
GHB5
GHN
Growth hormone 1
Growth hormone
Growth hormone B5
Growth hormone, normal
Growth hormone, pituitary
HG1
hGH-N
IGHD1B
Pituitary growth hormone
RNG
- 免疫原：
- Synthesized peptide derived from human Anti-HumanPlacental lactogen AA range: 150-217
- 特异性：
- The antibody can recognize human Placental lactogen and GH protein.
- 组成：
- PBS, pH7.2, 0.03% Porcolin 300, containing stabilizing protein
- 来源：
- Mouse, Monoclonal/IgG1, Kappa
- 稀释：
- IHC 1:200-400, ELISA 1:5000-20000
- 纯化工艺：
- The antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen.
- 储存：
- -15°C to -25°C/1 year(Do not lower than -25°C)
- 背景：
- The protein encoded by this gene is a member of the somatotropin/prolactin family of hormones which play an important role in growth control. The gene, along with four other related genes, is located at the growth hormone locus on chromosome 17 where they are interspersed in the same transcriptional orientation; an arrangement which is thought to have evolved by a series of gene duplications. The five genes share a remarkably high degree of sequence identity. Alternative splicing generates additional isoforms of each of the five growth hormones, leading to further diversity and potential for specialization. This particular family member is expressed in the pituitary but not in placental tissue as is the case for the other four genes in the growth hormone locus. Mutations in or deletions of the gene lead to growth hormone deficiency and short stature. [provided by RefSeq, Jul 2008],
- 功能：
- alternative products:Additional isoforms seem to exist,disease:Defects in GH1 are a cause of isolated growth hormone deficiency type IB (IGHD IB) [MIM:262400]; also known as pituitary dwarfism I. IGHD IB is an autosomal recessive deficiency of GH which causes short stature.,disease:Defects in GH1 are a cause of isolated growth hormone deficiency type II (IGHD II) [MIM:173100]. IGHD II is an autosomal dominant deficiency of GH which causes short stature.,disease:Defects in GH1 are the cause of Kowarski syndrome [MIM:262650]; also known as pituitary dwarfism VI.,disease:Defects in GH1 may be a cause of short stature [MIM:604271]. Short stature is defined by a subnormal rate of growth.,function:Plays an important role in growth control. Its major role in stimulating body growth is to stimulate the liver and other tissues to secrete IGF-1. It stimulates both the differentiation and prolifera
- Human pituitary adenoma tissue was stained with Anti-GH + hPL (ABT540) Antibody
- Human placenta tissue was stained with Anti-GH + hPL (ABT540) Antibody
