KALIG-1 rabbit pAb - ES2666

KALIG-1 rabbit pAb

Sizes: 50μL, 100μL

Catalogue Numbers: ES2666-50, ES2666-100

Citations, Manuals and MSDS Available upon request.

Background: Mutations in this gene cause the X-linked Kallmann syndrome. The encoded protein is similar in sequence to proteins known to function in neural cell adhesion and axonal migration. In addition, this cell surface protein is N-glycosylated and may have anti-protease activity. [provided by RefSeq, Jul 2008],

Alternate Name: KAL1; ADMLX; KAL; KALIG1; Anosmin-1; Adhesion molecule-like X-linked; Kallmann syndrome protein

Source: Rabbit

Applications: WB; IHC

Dilution: WB 1:500-2000; IHC-p 1:50-300

Reactivity: Human; Rat; Mouse;

Immunogen: The antiserum was produced against synthesized peptide derived from human KAL1. AA range:151-200

Storage and Stability: -20°C/1 year

Clonality: Polyclonal

Isotype: IgG

Concentration: 1 mg/ml

Observed Band (KD): 76kD

Human Gene ID: 3730

Human SWISS Prot NO: P23352

Subcellular Location: Cell membrane; Peripheral membrane protein. Secreted. Proteolytic cleavage may release it from the cell surface into the extracellular space.

Research Use Only