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FAM96B Rabbit anti-Human, Polyclonal, Bioss
SDP

Rabbit Polyclonal Antibody

Supplier:  Bioss BS9729R

Encompass_Preferred

Catalog No. 50-198-9295


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Description

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

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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