SLC25A4 antibody (AA 40-298)

Catalog No. ABIN3022646

The Rabbit Polyclonal anti-SLC25A4 antibody has been validated for WB and IF. It is suitable to detect SLC25A4 in samples from Human.

Quick Overview for SLC25A4 antibody (AA 40-298) (ABIN3022646)

Target: SLC25A4 (Solute Carrier Family 25 (Mitochondrial Carrier, Adenine Nucleotide Translocator), Member 4 (SLC25A4))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLC25A4 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF)

Product Details anti-SLC25A4 Antibody

Binding Specificity: AA 40-298

Sequence: HASKQISAEK QYKGIIDCVV RIPKEQGFLS FWRGNLANVI RYFPTQALNF AFKDKYKQLF LGGVDRHKQF WRYFAGNLAS GGAAGATSLC FVYPLDFART RLAADVGKGA AQREFHGLGD CIIKIFKSDG LRGLYQGFNV SVQGIIIYRA AYFGVYDTAK GMLPDPKNVH IFVSWMIAQS VTAVAGLVSY PFDTVRRRMM MQSGRKGADI MYTGTVDCWR KIAKDEGAKA FFKGAWSNVL RGMGGAFVLV LYDEIKKYV

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 40-298 of human SLC25A4/ANT1 (NP_001142.2).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000,IF,1:50 - 1:200

Restrictions: For Research Use only

Handling

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for SLC25A4

Target: SLC25A4 (Solute Carrier Family 25 (Mitochondrial Carrier, Adenine Nucleotide Translocator), Member 4 (SLC25A4))

Alternative Name: SLC25A4

Background: This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Mutations in this gene have been shown to result in autosomal dominant progressive external opthalmoplegia and familial hypertrophic cardiomyopathy.,SLC25A4,AAC1,ANT,ANT 1,ANT1,MTDPS12,MTDPS12A,PEO2,PEO3,PEOA2,T1,Signal Transduction,Cell Biology & Developmental Biology,Apoptosis,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Warburg Effect,Neuroscience,Neurodegenerative Diseases,SLC25A4

Molecular Weight: 33 kDa

Gene ID: 291

UniProt: P12235

Pathways: Proton Transport, Dicarboxylic Acid Transport