Rabbit Anti-FAM189A1 antibody

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F1891_HUMAN; FAM189A1; KIAA0574; Protein FAM189A1; TMEM228; Transmembrane protein 228.

Cat:

SL14767R

Species Reactivity：

(predicted: Human,Mouse,Rat,Chicken,Dog,Pig,Horse,Rabbit,Guinea Pig,)

Immunogen：

KLH conjugated synthetic peptide derived from human FAM189A1:121-220/539

Format：

Liquid

Storage instructions：

Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

Concentration：

1mg/ml

Clonality：

Polyclonal

Isotype：

IgG

Applications：

WB=1:500-2000IHC-P=1:100-500IHC-F=1:100-500ICC=1:100-500IF=1:100-500（Paraffin sections need to do antigen repair）not yet tested in other applications.optimal dilutions/concentrations should be determined by the end user.

Host：

Rabbit

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Unit:

Price: $228.00

Product PDFs

Datasheet: Down Datasheet

Other Information
Citations
Protein Attributes
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FAM189A1 is a 539 amino acid multi-pass membrane protein that exists as two alternatively spliced isoforms. The gene encoding FAM189A1 maps to human chromosome 15, which encodes more than 700 genes and is made up of approximately 106 million base pairs. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.

Subcellular Location:
Membrane.

Similarity:
Belongs to the FAM189 family.

SWISS:
O6064

Gene ID:
23359

Database links:

Entrez Gene: 23359 Human

SwissProt: O6064 Human

Unigene: 383564 Human

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