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ELK Biotechnology
SKU:ES14242
PC11X rabbit pAb
PC11X rabbit pAb
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$250.00 USD
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Applications: WB
Reactivity: Human;Rat;Mouse;
Source: Rabbit
Dilution: WB 1：500-2000
Immunogen: Synthesized peptide derived from human PC11X AA range: 836-886
Storage_stability: -20°C/1 year
Clonality: Polyclonal
Isotype: IgG
Concentration: 1 mg/ml
Human_gene_id: 27328
Human_swiss_prot_no: Q9BZA7
Subcellular_location: Cell membrane ; Single-pass type I membrane protein .
Background: This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The encoded protein consists of an extracellular domain containing 7 cadherin repeats, a transmembrane domain and a cytoplasmic tail that differs from those of the classical cadherins. The gene is located in a major X/Y block of homology and its Y homolog, despite divergence leading to coding region changes, is the most closely related cadherin family member. The protein is thought to play a fundamental role in cell-cell recognition essential for the segmental development and function of the central nervous system. Disruption of this gene may be associated with developmental dyslexia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014],
Reactivity: Human;Rat;Mouse;
Source: Rabbit
Dilution: WB 1：500-2000
Immunogen: Synthesized peptide derived from human PC11X AA range: 836-886
Storage_stability: -20°C/1 year
Clonality: Polyclonal
Isotype: IgG
Concentration: 1 mg/ml
Human_gene_id: 27328
Human_swiss_prot_no: Q9BZA7
Subcellular_location: Cell membrane ; Single-pass type I membrane protein .
Background: This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The encoded protein consists of an extracellular domain containing 7 cadherin repeats, a transmembrane domain and a cytoplasmic tail that differs from those of the classical cadherins. The gene is located in a major X/Y block of homology and its Y homolog, despite divergence leading to coding region changes, is the most closely related cadherin family member. The protein is thought to play a fundamental role in cell-cell recognition essential for the segmental development and function of the central nervous system. Disruption of this gene may be associated with developmental dyslexia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014],
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