PKD1L2 antibody (AA 2351-2459) (Biotin)

Catalog No. ABIN6944563

Product Details anti-PKD1L2 Antibody (Biotin)

Target: PKD1L2 (Polycystic Kidney Disease 1-Like 2 (PKD1L2))

Binding Specificity: AA 2351-2459

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PKD1L2 antibody is conjugated to Biotin

Application: ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human PKD1L2

Isotype: IgG

Application Details

Application Notes: IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for PKD1L2

Target: PKD1L2 (Polycystic Kidney Disease 1-Like 2 (PKD1L2))

Alternative Name: PKD1L2 (PKD1L2 Products)

Synonyms: 1700126L06Rik antibody, PC1L2 antibody, polycystic kidney disease 1 like 2 antibody, polycystin 1 like 2 (gene/pseudogene) antibody, Pkd1l2 antibody, PKD1L2 antibody

Background:

Synonyms: PC1 like 2 protein, PC1-like 2 protein, PK1L2_HUMAN, PKD1L 2, Pkd1l2, Polycystic kidney disease 1 like protein 2, Polycystic kidney disease 1-like protein 2, Polycystic kidney disease protein 1-like 2, Polycystin 1 like 2, Polycystin-1L2.

Background: This gene encodes a member of the polycystin protein family. The encoded protein contains 11 transmembrane domains, a latrophilin/CL-1-like GPCR proteolytic site (GPS) domain, and a polycystin-1, lipoxygenase, alpha-toxin (PLAT) domain. This protein may function as a component of cation channel pores. This gene appears to be a polymorphic pseudogene in humans, where some individuals contain a non-functional allele. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]

Gene ID: 114780

UniProt: Q7Z442