Rabbit Anti-FAM49B antibody

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BM 009; FA49B_HUMAN; Fam49b; Family with sequence similarity 49, member B; L1; Protein FAM49B.

Cat:

SL16002R

Species Reactivity：

(predicted: Human,Mouse,Rat,Chicken,)

Immunogen：

KLH conjugated synthetic peptide derived from human FAM49B:251-324/324

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=1:500-2000ELISA=1:5000-10000IHC-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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Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The FAM49B gene product has been provisionally designated FAM49B pending further characterization.

Similarity:
Belongs to the FAM49 family.

SWISS:
Q9NUQ9

Gene ID:
51571

Database links:

Entrez Gene: 51571 Human

SwissProt: Q9NUQ9 Human

Unigene: 126941 Human

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