GNRPX Polyklonale Antilichaam, PerCP Vervoeging

PLEKHJ1 is a 149 amino acid phosphoprotein that contains one PH (pleckstrin homology) domain and is expressed in testis and liver. The gene that encodes PLEKHJ1 maps to human chromosome 19, which consists of approximately 63 million bases and makes up over 2% of human genomic DNA. Chromosome 19 contains the greatest gene density of the human chromosomes and is the genetic home for a number of immunoglobulin superfamily members, including killer cell and leukocyte Ig-like receptors, ICAMs, the CEACAM and PSG families, and Fc?receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes are also linked to chromosome 19.

Guanine nucleotide releasing protein x; Guanine nucleotide-releasing protein x; Likely ortholog of mouse guanine nucleotide releasing protein x; PH domain containing family J member 1; PH domain-containing family J member 1; PKHJ1_HUMAN; Pleckstrin homology domain containing family J member 1; Pleckstrin homology domain-containing family J member 1; PLEKHJ 1; PLEKHJ1; 9530063M10Rik; FLJ10297.

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GNRPX

PerCP

KLH conjugated synthetic peptide derived from human GNRPX/PLEKHJ1

IF (IHC-P), IF (IHC-F), IF (ICC)

Purified by Protein A.

482nm/677nm

1µg/µl

IF (IHC-P) (1:50-200), IF (IHC-F) (1:50-200), IF (ICC) (1:50-200)

Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Unmodified

Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

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Human, Mouse, Rat, Cow, Sheep, Pig