CDH15 Antibody (PACO01052)
- SKU:
- PACO01052
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Application:
- ELISA
- Application:
- WB
- Application:
- IHC
- Antibody type:
- Polyclonal
- Conjugation:
- Unconjugated
Frequently bought together:
Description
抗体名: | CDH15 Antibody |
抗体コード: | PACO01052 |
サイズ: | 50ug |
宿主種: | Rabbit |
申し込み: | ELISA, WB, IHC |
推奨される希釈: | WB:1:500-1:2000, IHC:1:100-1:300 |
反応性: | Human, Mouse, Rat |
免疫原: | synthesized peptide derived from the N-terminal region of human M-cadherin. |
憲法: | Liquid |
ストレージバッファ: | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
精製方法: | The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. |
抗体のクローン性: | Polyclonal |
アイソタイプ: | IgG |
Conjugate: | Non-conjugated |
シノニム: | CDH15; CDH14; CDH3; Cadherin-15; Cadherin-14; Muscle cadherin; M-cadherin |
UniProt Protein Function: | CDH15: Cadherins are calcium-dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types. M-cadherin is part of the myogenic program and may provide a trigger for terminal muscle differentiation. A chromosomal aberration involving CDH15 and KIRREL3 is found in a patient with severe mental retardation and dysmorphic facial features. Translocation t(11;16)(q24.2;q24). Defects in CDH15 are the cause of mental retardation autosomal dominant type 3 (MRD3). Mental retardation is characterized by significantly sub-average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. |
UniProt Protein Details: | Protein type:Membrane protein, integral Chromosomal Location of Human Ortholog: 16q24.3 Cellular Component: plasma membrane; integral to membrane; caveola; neuromuscular junction Molecular Function:calcium ion binding Biological Process: intercellular junction assembly and maintenance; muscle cell differentiation; positive regulation of muscle cell differentiation; homophilic cell adhesion; cell adhesion Disease: Mental Retardation, Autosomal Dominant 3 |
NCBI Summary: | This gene is a member of the cadherin superfamily of genes, encoding calcium-dependent intercellular adhesion glycoproteins. Cadherins consist of an extracellular domain containing 5 cadherin domains, a transmembrane region, and a conserved cytoplasmic domain. Transcripts from this particular cadherin are expressed in myoblasts and upregulated in myotubule-forming cells. The protein is thought to be essential for the control of morphogenetic processes, specifically myogenesis, and may provide a trigger for terminal muscle cell differentiation. [provided by RefSeq, Jul 2008] |
UniProt Code: | P55291 |
NCBI GenInfo Identifier: | 1705553 |
NCBI Gene ID: | 1013 |
NCBI Accession: | P55291.1 |
UniProt Related Accession: | P55291 |
Molecular Weight: | 88,916 Da |
NCBI Full Name: | Cadherin-15 |
NCBI Synonym Full Names: | cadherin 15, type 1, M-cadherin (myotubule) |
NCBI Official Symbol: | CDH15 |
NCBI Official Synonym Symbols: | CDH3; CDHM; MCAD; MRD3; CDH14 |
NCBI Protein Information: | cadherin-15; cadherin-3; cadherin-14; muscle-cadherin |
UniProt Protein Name: | Cadherin-15 |
UniProt Synonym Protein Names: | Cadherin-14; Muscle cadherin; M-cadherin |
Protein Family: | Cadherin |
UniProt Gene Name: | CDH15 |
UniProt Entry Name: | CAD15_HUMAN |