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FAM96B Rabbit anti-Human, Polyclonal, Bioss

Rabbit Polyclonal Antibody
Supplier: Bioss BS9729R

Description
Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn′s disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The FAM96B gene product has been provisionally designated FAM96B pending further characterization.Specifications
FAM96B | |
Polyclonal | |
Unconjugated | |
CIAO2B | |
1110019N10Rik; CGI-128; CIAB; Ciao2b; Cytosolic iron-sulfur assembly component 2B; FAM96B; family with sequence similarity 96 member B; family with sequence similarity 96, member B; HSPC118; Mip18; Mitotic spindle-associated MMXD complex subunit MIP18; MSS19-interacting protein of 18 kDa; Protein FAM96B; RGD1311762 | |
Rabbit | |
Protein A | |
RUO | |
51647 | |
-20°C | |
Liquid |
Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot | |
1 μg/mL | |
PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH | |
Q9Y3D0 | |
CIAO2B | |
KLH conjugated synthetic peptide derived from human FAM96B. | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
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