抗体

anti-ALX Homeobox 4 (ALX4) (AA 249-275), (Center) antibody

ABIN654344

400微升

291.5美元

多克隆

兔

nonconjugated

RB28072

免疫印迹, 流式细胞仪, 流式细胞仪

anti-ALX Homeobox 4 (ALX4) (AA 249-275), (Center) antibody

兔

多克隆

ALX4

Primary

400微升

291.5美元

19783719,19336475

ALX4 Antibody (Center) (ABIN654344) flow cytometric analysis of MDA-MB435 cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

RB28072

Ig

This gene encodes a paired-like homeodomain transcription factor expressed in the mesenchyme of developing bones, limbs, hair, teeth, and mammary tissue. Mutations in this gene cause parietal foramina 2 (PFM2), an autosomal dominant disease characterized by deficient ossification of the parietal bones. Mutations in this gene also cause a form of frontonasal dysplasia with alopecia and hypogonadism, suggesting a role for this gene in craniofacial development, mesenchymal-epithelial communication, and hair follicle development. Deletion of a segment of chromosome 11 containing this gene, del(11)(p11p12), causes Potocki-Shaffer syndrome (PSS), a syndrome characterized by craniofacial anomalies, mental retardation, multiple exostoses, and genital abnormalities in males. In mouse, this gene has been shown to use dual translation initiation sites located 16 codons apart. [provided by RefSeq]. Synonyms: Homeobox protein aristaless-like 4,ALX4,KIAA1788

This ALX4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 249-275 AA from the Central region of human ALX4.

AA 249-275,Center

人类

PBS with 0.09 % (W/V) sodium azide

0.34毫克/毫升

流式细胞仪(流式细胞仪), 免疫印迹(免疫印迹)

Q9H161