Anti-ALX4 Antibody (CAB2834)
- SKU:
- CAB2834
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Epigenetics and Nuclear Signaling
Frequently bought together:
Description
抗体名: | Anti-ALX4 Antibody |
抗体コード: | CAB2834 |
抗体サイズ: | 20uL, 50uL, 100uL |
申し込み: | WB IHC |
反応性: | Human, Mouse, Rat |
宿主種: | Rabbit |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-220 of human ALX4 (NP_068745.2). |
申し込み: | WB IHC |
推奨希釈: | WB 1:500 - 1:2000 IHC 1:50 - 1:200 |
反応性: | Human, Mouse, Rat |
ポジティブサンプル: | HepG2 |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-220 of human ALX4 (NP_068745.2). |
精製方法: | Affinity purification |
ストレージバッファ: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
アイソタイプ: | IgG |
順序: | MNAE TCVS YCES PAAA MDAY YSPV SQSR EGSS PFRA FPGG DKFG TTFL SAAA KAQG FGDA KSRA RYGA GQQD LATP LESG AGAR GSFN KFQP QPST PQPQ PPPQ PQPQ QQQP QPQP PAQP HLYL QRGA CKTP PDGS LKLQ EGSS GHSA ALQV PCYA KESS LGEP ELPP DSDT VGMD SSYL SVKE AGVK GPQD RASS DLPS PLEK ADSE SNKG KKRR NRTT |
遺伝子ID: | 60529 |
Uniprot: | Q9H161 |
セルラーロケーション: | Nucleus |
計算された分子量: | 44kDa |
観察された分子量: | 44kDa |
同義語: | ALX4, CRS5, FND2 |
バックグラウンド: | 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. |
UniProt Code: | Q9H161 |
NCBI GenInfo Identifier: | 254763249 |
NCBI Gene ID: | |
NCBI Accession: | Q9H161.2 |
Molecular Weight: | 44kDa |
NCBI Full Name: | Homeobox protein aristaless-like 4 |
UniProt Protein Name: | Homeobox protein aristaless-like 4 |
Protein Family: | Homeobox protein |
UniProt Gene Name: | ALX4 |
UniProt Entry Name: | ALX4_HUMAN |
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